Clinical relevance of biomarkers, new therapeutic approaches, and role of post-translational modifications in the pathogenesis of Alzheimer’s disease

Introduction

Alzheimer’s disease (AD) is a neurodegenerative disorder associated with diminished regenerative capacity of neurons and impaired cognitive functions including learning and memory (Galimberti and Scarpini, 2012; Haque and Levey, 2019; Chatterjee et al., 2020). Nearly 35 million people are suffering from AD worldwide and is estimated to be doubled by 2030 (Alzheimer’s Association, 2019; Haque and Levey, 2019). The nature of this disease demands proper and long-term medical care which has accounted for an estimated cost of $195 billion in 2019 and is expected to rise to $1 trillion by 2050 (Alzheimer’s Association, 2019). Various factors contribute to AD-related dementia and impairment of cognitive functions, however, extracellular amyloid beta (Aβ) plaques and intracellular aggregates of hyperphosphorylated tau proteins also called neurofibrillary tangles (NFTs) are the two major histopathological hallmarks of AD (Mayeux and Stern, 2012; Xu et al., 2012; Kametani and Hasegawa, 2018; Janeiro et al., 2021). Accumulation of amyloid beta (Aβ) plaques and NFTs initiate a cascade of events, resulting firstly in synaptic dysfunction, axonal degeneration and impaired cellular communication, and followed subsequently as the disease progresses by gliosis, neurodegeneration and widespread neuronal death (Wang et al., 2013; Hampel et al., 2015; Li et al., 2015; Pini et al., 2016; Knezevic et al., 2018). Although accumulation of Aβ deposits and NFTs are the pathological hallmarks of AD and have drawn the special attention of researchers in the search for biological markers, it is clear now that the disease begins decades before the onset of any clinical symptoms. To predict, diagnose, or monitor the progression of AD disease biomarkers are considered useful in every step of patient care. As disease symptoms are subjective, biomarkers provide an objective, measurable way to characterize the disease. Biomarkers for Alzheimer’s disease aim to facilitate early disease prognosis and makes it possible to determine the progression of disease during initial stage and evaluate response to existing and future treatments. Also, biomarkers are likely to predict clinical benefit and support accelerated or traditional drug approval, respectively. There is an unmet need for identification of such clinical biomarker for Alzheimer’s disease.

Major proteins and enzymes involved in Alzheimer’s progression: Role of amyloid-beta precursor protein, secretase, Tau, beta-site amyloid-beta precursor protein-cleaving enzyme, Apo E, PS1/2, and microglia

Amyloid-beta precursor protein and secretase enzymes

Amyloid-beta precursor protein (APP) encoded by a gene APP (located on chromosome 21) is a ubiquitous type-1 transmembrane protein with three splice variants: APP695, APP751, and APP770 expressed mostly in neurons, astrocytes, and vascular endothelial cells respectively (Miura et al., 2020; Zhao et al., 2020). Although the exact functions of APP are not known, however, its expression increases during differentiation of neurons and synapse formation, and declines once mature connections are established, suggesting the role of APP in aging and development (Chen et al., 2017). Under normal conditions, APP undergoes non-pathogenic processing by involving two important enzymes α-and γ-secretase. These enzymes cleave the APP within the Aβ domain resulting into non-amyloidogenic fragments along with soluble amyloid precursor protein fragments α (sAPPα) and C-terminal fragments (CTFs). In diseased conditions, a different set of enzymes including β-and γ-secretase to cleave the APP in such a way that it generates the neurotoxic Aβ peptides (40–42 amino acid long peptides), along with soluble amyloid precursor protein fragments β (sAPPβ) and CTFs (Nesterova et al., 2019). Various studies have shown a link between the mutations of APP and AD; for example 10–15% cases of early-onset-familial Alzheimer’s disease (EOFAD) are reported to be caused by APP gene mutations (Hooli and Tanzi, 2016). Such mutations appear to influence the biology of Aβ by promoting local oligomer/fibril formation or changing the propensity of Aβ to bind to other proteins and affecting Aβ clearance. This ability of APP to undergo cleavage using different set of enzymes to form either soluble or pathogenic amyloid-beta (Aβ) peptides makes APP as a main target protein in AD progression. Any mutation in APP and in the proteins that regulate APP endocytosis and processing in neurons leading to disturbed APP-related intracellular signaling pathways can be used as a biomarker during early stages of AD.

Tau protein

Tau is a microtubule-associated protein involved in the stabilization of microtubules by promoting their polymerization. The association of tau protein with the microtubules is involved in regulating the axonal transport as well as neuronal cytoskeleton (Zhou et al., 2018). Six different isoforms of tau are usually expressed in normal mature human brains however they are found to be abnormally hyperphosphorylated in AD brains. Any unusual alterations in the structural conformation or phosphorylation events of tau impact its binding affinity with microtubule which leads to its toxic aggregation in the form of neurofibrillary tangles (NFTs) and paired helical filaments (PHFs). These NFTs which on aggregation attain the shape of PHFs are one among the major hallmarks seen in pathology of AD (Augustinack et al., 2002). Tau phosphorylation and its detailed role in the pathogenesis is included elsewhere under post-translational modifications (PTMs) in AD. Importantly, Hyper-phosphorylated tau is considered to be promising biomarker for monitoring the disease progression in AD.

Beta-site amyloid-beta precursor protein-cleaving enzyme

Beta-Site APP-cleaving enzyme (BACE) is a ubiquitously expressed membrane-bound aspartyl protease. It uses its proteolytic activity for the production of neuro-pathogenic Aβ peptides. There are four splice variants of BACE with 501, 476, 457, and 432 amino acids. Among these variants 501 variant is having the highest degree of proteolytic activity on Aβ amyloid substrate (Mowrer and Wolfe, 2008). The production of Aβ peptides from its precursor APP occurs in two sequential proteolytic cleavages. First cleavage is catalyzed by BACE in which BACE cleaves the ectodomain of APP generating a C99 membrane-bound C-terminal fragment and the second proteolytic reaction is carried out by γ-secretase which further processes a C99 fragment leading to the formation of Aβ peptides (Bolduc et al., 2016). In AD patients BACE is highly expressed in various parts of the brain especially in brain cortex and cerebrospinal fluid (CSF) (Hampel et al., 2020). The increased expression of BACE can serve as an early biomarker in detection of AD (Blennow et al., 2010; Evin et al., 2010), and its increased expression has been directly co-related with the age of the patient and stress level (O’brien and Wong, 2011). BACE1 protein concentrations and rates of enzyme activity are promising candidates among biological markers in clinical trials investigating the role of BACE1 inhibitors in regulating APP processing.

Apolipoprotein E

In the central nervous system (CNS), apolipoprotein E (ApoE) is mostly synthesized and produced by astrocytes to transport cholesterol to neurons via ApoE receptors (Bu, 2009). ApoE is composed of 299 amino acids and exists in three isoforms in humans; ApoE2, ApoE3, and ApoE4. The single amino acid differences alter the structure of these isoforms and influences their functional abilities (Frieden and Garai, 2012). The ApoE4 isoform represents the most significant risk factor for late-onset Alzheimer disease (LOAD) (Corder et al., 1993; Mahoney-Sanchez et al., 2016). The individuals carrying the rare E2 variant are less likely to develop AD and E3 represents the most common but non-pathogenic isoform of ApoE (Serrano-Pozo et al., 2015). Although number of studies have been conducted to understand the mechanism of action of different variants of ApoE, but further investigation and research is needed to fully understand the differential effects of ApoE isoforms on Aβ aggregation and clearance in AD pathogenesis (Kim et al., 2009; Husain et al., 2021). In an interesting study, the total ApoE and ApoE4 plasma proteins were assessed using Australian Imaging, Biomarkers and Lifestyle (AIBL) study of aging and the result were assessed by Positron Emission Tomography (PET) using Pittsburgh compound B (PiB). The levels of these plasma proteins were compared with cerebral Aβ load, and it was found that both the total ApoE as well as ApoE4 levels are significantly lowered in AD patients. From ApoE genotyping, the protein (ApoE) levels were significantly lower among E4 homozygous individuals and in APOE E3/E4 heterozygote carriers, ApoE4 levels decreased, indicating that ApoE3 levels increase with disease. This study suggests that ApoE, ApoE3, and ApoE4 can be used as AD biomarkers and possible therapeutic drug targets (Gupta et al., 2011; Soares et al., 2012).

Presenilin 1

Presenilin 1 protein encoded by PSEN1 gene is located on chromosome 14 and forms an important component of the γ-secretase complex, which cleaves APP into Aβ fragments (Steiner et al., 2008). It is mostly expressed in endoplasmic reticulum and helps in protein processing (Bezprozvanny and Mattson, 2008). The importance of PSEN1 gene in AD is evident from the fact that it accounts for about 50% cases of early-onset Alzheimer’s disease (EOAD), with complete penetrance (Giri et al., 2016). Mutation in PSEN1 leads to mutations in γ-secretase and increase in the Aβ42/40 ratio resulting in cotton wool plague formation (Zhang et al., 2015; Miki et al., 2019). Only few mutations are insertions and deletions, majority of PSEN1 mutations are missense. PSEN1 mutations not only affect the activity of γ-secretase enzyme but also directly affect the neuronal functioning by controlling the activity of GSK-3β and kinesin I (Giri et al., 2016). More than 295 pathogenic mutations have been identified in PSEN1, of which 70% mutations occur in exons 5, 6, 7, and 8. Studies using genetically modified mice have shown that mutations in PSEN1 lead to impaired Aβ production and increased ratio of Aβ42/Aβ40 (Xia et al., 2015). Recent studies that investigated potential relationships between the molecular composition of FAD-linked Aβ profiles and disease severity by analyzing Aβ profiles generated by 25 mutant PSEN1/GSECs that span a wide range of AAOs, revealed that full spectrum of Aβ profiles (including Aβ37, Aβ38, Aβ40, Aβ42, and Aβ43) better reflects mutation pathogenicity. Furthermore, this study suggested Aβ(37 + 38 + 40)/Aβ(42 + 43) ratio better at predicting the age at disease onset (Petit et al., 2022). Presently, PSEN1 gene is considered as the most common cause of familial Alzheimer’s disease (FAD). However, a recent studies (Sun et al., 2017) contradicts the role of PSEN1 in AD progression by increasing the Aβ42 production (Hardy and Selkoe, 2002) and therefore is a matter of a debate in the scientific world.

Presenilin 2

Presenilin 2 protein encoded by PSEN2 gene is located on chromosome 1 is similar in structure and function to PSEN1 (Ridge et al., 2013). Similar to PSEN1, it also forms the important component of the γ secretase complex and any mutation in PSEN2 alters the activity of γ secretase leading to elevated ratio of Aβ42/40 (Wakabayashi and De Strooper, 2008). Despite close homology between the two, mutations in PSEN2 are less toxic and less common than PSEN1, but neuritic plaque accumulation and neurofibrillary tangle (NFT) formation have been found in some people with PSEN2 mutations (Giri et al., 2016). Efforts to develop disease-modifying therapies for AD have been heavily focused on the amyloid hypothesis but repeated failures in late-stage clinical trials based on these hypotheses heighten the urgency to explore alternative approaches. Thus, therapeutic strategies aimed at restoring secretase activities by involving modifications or mutations at the levels of PSN1 and PSN2 offer a valid and complementary approach to develop disease modifying treatments for FAD.

Microglial role in Alzheimer’s disease

Microglia, a type of neuroglia (glial cells), forms the innate immune system of our central nervous system (CNS). Proliferation, activation, and concentration of these glial cells in the brain around amyloid plaques, is a prominent feature of AD. Data from human genetic studies also suggest the role of these cells in AD progression. Under normal conditions, microglia protect against AD, however, impaired microglial activities lead to increased risk of AD progression. Activated microglial cells can be harmful and mediate loss of synaptic junctions via complement-dependent mechanisms, increase tau phosphorylation and enhance inflammatory responses against neurons leading to activation of neurotoxic astrocytes (Hansen et al., 2018). The role of microglia in forming neuritic plaques was described long back by Alois Alzheimer himself (Alzheimer et al., 1995; Graeber et al., 1997) and further studies have shown the involvement of both reactive astrocytes and microglia in deposition of Aβ plagues (Verkhratsky et al., 2016). In AD patients, the microglia interact with the amyloid peptides, APP, and neurofibrillary tangles during early phase of AD, and their activation promote Aβ clearance through microglia’s scavenger receptors, and thus acts as a hurdle in the progression of AD. The Aβ activation induced continuous activation of microglia involving CD36, Fc receptors, toll-like receptors (TLRs), and complement receptors advanced glycation end products (RAGE), promote Aβ production while hampering Aβ clearance, which ultimately causes neuronal damage (Wang et al., 2015). In a study done on post-mortem brain sections taken from AD patient, it was found that increased microglia activation begins with amyloid NP deposition and the increase was found to be directly related to the part of brain involved in AD (Xiang et al., 2006). Thus, activation of microglia in brain tissues, such as hippocampi, can serve as an inflammatory biomarker for AD.

Major sources and methods for isolation of potential biomarkers for Alzheimer’s disease

One of the major challenges in the treatment of Alzheimer’s disease is the lack of sensitive and specific biomarkers. Multiple studies have argued that AD begins decades before the onset of clinical symptoms and accumulation of Aβ deposits and NFTs-pathological hallmarks of AD. Clinically relevant biomarkers are expected to be useful in detecting the preclinical as well as symptomatic stages of AD. Such clinically relevant biomarkers used in the validation of AD are structured through a road map called the Strategic Biomarker Roadmap (SBR), initiated in 2017 and according to recent reports is still valid for the assessment of biomarkers of tauopathy, as well as that of the other diagnostic biomarkers of AD and related disorders (Boccardi et al., 2021). Moreover, biomarkers would be significantly helpful to predict, diagnose, or monitor the progression of AD disease during initial stage, and in evaluating response to existing and future treatments. Till date different methods have been followed to access and isolate the different biomarkers for AD.

Potential biomarkers for Alzheimer’s disease from cerebrospinal fluid

Although advanced neuroimaging techniques have been very useful in assessing structural and physiological changes in the brains of AD patients, clinical biomarkers still represent the most convenient and direct means to monitor the disease state. Despite the fact that PET and cerebrospinal fluid (CSF) biomarkers are useful information for the diagnosis of AD, these methods have limited use due to their sophistication, invasiveness, and high cost. In the search for biological markers of AD, Aβ42, t-Tau, and p-Tau have drawn the special attention of researchers. Various types of brain specific biomarkers associated with AD are shown in Figure 1, CSF specific biomarkers for AD are listed in Table 1 and diagnostic platforms based on four chief biomarkers for AD along with various parameter are listed in Table 2. Aβ42, T-tau and P-tau biomarkers can predict progression from preclinical to clinical AD (Mattsson et al., 2018). The levels and variations of Aβ in CSF have been an essential hallmark feature of AD-type dementia (d’Abramo et al., 2020). It has been suggested that the ratio of CSF Aβ42/Aβ40 can be a superior biomarker because this ratio is quite useful in the differentiation of AD from other non-Alzheimer’s related cognitive changes like the subcortical deficits related to vascular diseases. Aβ42 levels in the CSF are generally lower in comparison to the controls and Aβ42 levels decrease substantially with an increase in disease progression (d’Abramo et al., 2020). The other biomarkers like YKL-40 (Chitinase-3-protein like), VILIP-1 (VLP-1) and, NFL are associated with glial inflammation, neuronal damage and non-specific marker for neurodegeneration respectively can also be used for the diagnosis but the limit of detection (LOD) and accuracy should be validated first in order to gain the specificity (Gaiottino et al., 2013; Olsson et al., 2016).

FIGURE 1

Figure 1. Brain specific biomarker associated with Alzheimer’s disease.

TABLE 1

Table 1. Biomarkers for Alzheimer’s disease (AD) in cerebrospinal fluid (CSF).

TABLE 2

Table 2. Sensing platforms based on four chief biomarkers associated with Alzheimer’s disease (AD) and their limit of detection (LOD).

Potential biomarkers for Alzheimer’s disease from blood

Blood-based biomarkers are more cost-effective than PET imaging, less invasive than CSF testing, and can be used as viable first-line tools in the multi-stage diagnostic processes (d’Abramo et al., 2020). Since blood testing is a part of clinical routines all over the world which require no special or further training, therefore, blood-based biomarkers for AD are more promising. Although, a lot of progress has been made in understanding the role of biomarkers in the pathophysiology of AD (Tables 1, 2), there is still a need for the development of blood-based biomarkers that can help in the early diagnosis of AD and to understand disease progression. Tau and β-Site APP Cleavage Enzyme 1 (BACE 1) to some levels are useful in this context (Snyder et al., 2014). Tau levels in the blood can be used to predict the onset of future cognitive decline and the levels of BACE1 activity in the blood can also be used to predict the progression of mild cognitive impairment to AD dementia (Hampel et al., 2018). Aβ peptides like Aβ1-42, Aβ1-40, and Aβ1-17 as well as tau are important blood biomarkers to detect AD and its progression. These peptides in plasma can be detected by immunoprecipitation and mass spectroscopy (Pannee et al., 2014; Ovod et al., 2017). It has been found that the plasma levels of Aβ-42, Aβ1-40, and Aβ1-42/Aβ1-40 are low in AD patients but show a significant correlation with CSF levels (Janelidze et al., 2016a). Blood levels of Aβ1-17 also play an important role in the diagnosis of AD. The ratio of free to cell-bound Aβ1-17 levels in the blood helped to understand the difference between healthy individuals and individuals with mild AD with high specificity and sensitivity (Snyder et al., 2014). Tau proteins in plasma have been quantified by sensitive immunoassay techniques and found to be increased in AD patients compared to controls (Zetterberg et al., 2013; Neergaard et al., 2018). Phosphorylated tau (p-tau) proteins are leading blood biomarkers that identify AD, and its underlying pathology. It also highlights future risks of AD. Plasma p-tau (p-tau217 and p-tau181) highlights AD in dementia cases with high accuracy and can also be validated by neuropathological studies. AD progression can be strongly predicted by even baseline increases of p-tau biomarkers However, assay platform comparisons and effects of covariates and accurate biomarker cut-offs for p-tau and Aβ are still lacking necessitating more studies in this direction in the context of Strategic Biomarker Roadmap (Ashton et al., 2021). Moreover, Aβ1–42, Aβ1–40 and phosphorylated tau represent post-translationally modified protein species this explains the involvement of PTMs as biomarkers in AD (Henriksen et al., 2014). Furthermore, recent studies suggested Aβ37/42 ratio could become an improved Aβ biomarker for Alzheimer’s disease of pathogenicity and clinical diagnosis (Liu et al., 2022). Other proteins like axonal protein and neurofilament light (NF-L) are found to be increased in the serum of AD patients and have been found to be comparable with plasma Aβ1–42/Aβ1–40 (Mattsson et al., 2017). However, high NFL-1 concentration in plasma is not associated only with AD but also with other neurodegenerative disorders (Progressive supranuclear palsy and corticobasal syndrome). Recently, investigators questioned if a panel of blood-based biomarkers instead of an individual biomarker could be more useful in the detection of AD. In this direction, O’Bryant used a different set of 30 serum proteins to develop an algorithm that could detect AD with 80% sensitivity and 91% specificity (O’Bryant et al., 2010). It was reported that a panel of three blood markers von Willebrand factor, cortisol, and oxidized LDL antibodies identified using multivariate data analysis, could distinguish between AD patients and normal ones with more than 80% accuracy (Laske et al., 2011). To some level, microRNAs and PTMs can also serve as biomarkers for AD. Alterations in microRNAs levels are reported to be associated with AD pathology and efforts are being made to monitor the changes in the individual miRNAs in blood as biomarkers (Henriksen et al., 2014). A decrease in miR-132-3p levels has been reported to be associated with AD due to the hyper-phosphorylation of tau (Lau et al., 2013). Interestingly, miR-125b and miR-26b have been reported to be increased in AD patients and both are associated with tau phosphorylation (Absalon et al., 2013; Ma et al., 2017). Blood biomarkers are reliable and promising in AD detection Anything that may interfere with the detection of AD biomarkers when their concentration is low in blood is taken care of by modern diagnostic platforms that work with high dilution and high amplification of the specific signal which allows the detection of picomolar/ml or even lesser concentrations of the target biomarker. It was shown that detection by immunoprecipitation followed by liquid chromatography-mass spectroscopy (IP-MS) is a high precision assay for plasma Aβ42-40 ratio, which predicts brain amyloidosis with 90% accuracy (d’Abramo et al., 2020). Recent clinic trials based on biomarker identification for Alzheimer’s disease are listed in Table 3.

TABLE 3

Table 3. List of natural products and synthetic drugs tested for identification of a reliable clinical biomarker in various clinical trials of Alzheimer’s disease.

Extracellular vesicles associated with Alzheimer’s disease

Extracellular vesicles (EV) or exosomes (EXOs) were initially considered as cellular trash bags. These lipid-based membrane-bound biological nanoparticles have now emerged as a new paradigm of cell-to-cell communication which has implications for both normal and pathological physiology (Raposo and Stahl, 2019). Recently, extracellular vesicles have been widely used as biomarkers and are found to play an important role in the pathogenesis of Alzheimer’s disease. The presence of disease-related proteins in these extracellular vesicles from AD patients have been actively studied to use them as biomarkers to predict the development of AD before the appearance of clinical symptoms (Lin et al., 2019). They are excreted in the urine and saliva of both healthy and diseased individuals which makes them an excellent choice for diagnostics in diseases like AD as compared to other invasive methods which require lumbar puncture or brain autopsy for diagnosis (Watson et al., 2019). EVs are released from various cell types including the cells associated with neuron-glia communication, neuronal progression, and regeneration from CNS (Surgucheva et al., 2012; Bronisz et al., 2014; Janas et al., 2016). It is widely accepted that EVs are good biomarkers but their nature, regulation, sorting and molecular composition need to be further investigated. Interestingly, the role of exosomes in stimulating aggregation of amyloid-beta (Aβ) peptides in vitro and in vivo was demonstrated and as was their role in the uptake of Aβ by cultured astrocytes and microglia under in vitro conditions (Dinkins et al., 2014). By preventing the secretion of EVs via inhibition of neutral sphingomyelinase 2 (nSMase2), a key regulatory enzyme generating ceramide from sphingomyelin, with GW4869, they observed a significant reduction of Aβ plaques in the mice brain. Moreover, exosomal markers such as Alix and flotillins have been found to be associated with the amyloid plaques of the brain of post-mortem tissues of human AD patients when compared to post-mortem samples of healthy individuals, thereby reflecting specific association of EVs with amyloid plaques (Hu et al., 2016). Further, an increase in levels of tau in exosomes have been reported in CSF at an early phase of AD (Saman et al., 2012; Asai et al., 2015). Levels of several exosomal miRNAs that are altered in AD points to their roles in regulating certain events related to AD neurodegeneration as the ability of miRNAs to target genes related to tau phosphorylation, APP processing, and apoptosis is already known (Liu et al., 2014; Ma et al., 2017). The miRNA-193b and miRNA-125b-5p are the two most common exosomal miRNAs identified and are reported to be expressed differentially in exosomes isolated from serum, plasma and CSF of AD patients (Soares Martins et al., 2021). Therefore, miRNA-193b and miRNA-125b-5p are thought to be potential putative peripheral biomarkers of AD pathogenesis. EVs as potential biomarkers for AD can open up a wide arena of discoveries associated with it; however, a proper evaluation and correlation is needed for it as well.

Circadian genes associated with Alzheimer’s disease

It has been reported that that the levels of the main risk factor for AD progression i.e., Aβ in the brain are regulated by circadian rhythms and the sleep-wake cycle (Kang et al., 2009). Circadian rhythms (CR) are biological clocks that coordinate internal time with the external environment to regulate various physiological processes like the sleep-wake cycle, mental, behavioral and physical changes. Circadian rhythms are managed by a molecular clock in the suprachiasmatic nucleus (SCN) that resides in the anterior part of the hypothalamus. Molecular clockwork consists of different core clock genes such as period circadian regulators 1 and 2 (PER1 and PER2), circadian locomotor output cycles kaput protein (CLOCK), brain and muscle ARNT-like 1 (BMAL1), cryptochrome circadian regulators 1 and 2 (CRY1 and CRY2), These genes are organized in a transcription-translation feedback loop that oscillates every 24 h. Any mutation or alteration in these genes or their subsequent proteins has functional impacts on the CR (Shkodina et al., 2021). Disruptions in CR cause cognitive impairment, psychiatric illness, metabolic syndromes, and are thus considered as a significant risk factor in the onset of cerebrovascular and neurodegenerative disorders such as Alzheimer’s, Parkinson’s, and Huntington’s diseases. Moreover, disrupted sleep wake-cycle and alterations in circadian rhythms are seen to lead to AD progression by dysfunctional tau metabolism. This is achieved by changing the conformation and solubility of tau in the brain involving the post-translational modifications by decreasing the activity of major regulators of tau phosphorylation, especially cyclin-dependent kinase 5 (cdk-5) (Di Meco et al., 2014). During the early development of AD, there is a disruption in the normal expression of clock genes (especially Cry1, Cry2, and Per1) not only in the central pacemaker but also in other brain areas like the cortex, hippocampus, and cerebellum supporting circadian regulation (Bellanti et al., 2017). Since sleep and circadian rhythm dysfunction (SCRD) are very common in the early stage of AD, it is considered as a potential early biomarker for detecting AD. A proper understanding of the circadian clock and investigations of core clock components including Bmal1, Clock, Per1, Per2, Cry1, Cry2, Rev-erbα, and Rorα by genomic, proteomic, and metabolomic studies and its influence on several key processes involved in neurodegeneration might be helpful to be manipulated at early stages to promote healthy brain aging and decrease the chances of AD progression on one hand and uncover their potential use as biomarkers and hallmarks of circadian disruption during early stages of Alzheimer’s disease progression.

Post-translational modifications in Alzheimer’s disease

Translated messages in the form of protein undergo important modifications usually after their synthesis. These post translational modifications (PTMs) usually occur in the various cellular compartments like the Endoplasmic reticulum, Golgi complex, Nucleus, as well as Cytoplasm (Blom et al., 2004). PTM’s play an important role in regulating the structure, localization and, activity of proteins (Deribe et al., 2010). PTMs impact the hydrophobicity of proteins and induce changes in their structural conformations and thus define protein function as well as their interactions with other proteins (Ravid and Hochstrasser, 2008; Ardito et al., 2017). PTMs involve the addition of varied chemical moieties to a target protein that include phosphate, acyl, methyl, and glycosyl groups catalyzed by specific enzymes. PTMs not only define the structural integrity of proteins, these modifications usually cause the proteins to lose or enhance their normal function as well (Santos and Lindner, 2017). Unusual PTMs of various proteins like APP, secretases, tau, various kinases, and phosphatases are linked to the development of neurodegenerative diseases. The appearance of NFTs, senile plaques and aggregation of toxic amyloid β peptides are some of the hallmarks of abnormal PTMs in Alzheimer’s disease. These posttranslational protein modifications are associated with memory weakening, cognitive impairments, reduced synaptic plasticity and thus rapid progression to AD (Chong et al., 2018). Exploring post-translational modifications and understanding their molecular mechanism will open a window to develop effective and rational therapeutic interventions to counter these neurodegenerative disorders. Various PTMs associated with AD are shown in Figure 2. PTM specific modifications associated with AD vs. normal brain are also shown in Figure 3 and discussed in detail here.

FIGURE 2

Figure 2. Various post-translational modifications (PTMs) associated with Alzheimer’s disease.

FIGURE 3

Figure 3. Post-translational modifications (PTM) specific modifications associated with Alzheimer’s disease vs. normal brain. (A) PTMs associated with Alzheimer’s disease. (B) Normal PTMs.

Phosphorylation

Phosphorylation is one of the most frequently occurring PTMs in proteome biology, and about 30% of proteins undergo such modifications (Sacco et al., 2012). It involves the addition of a phosphate group to amino acids particularly to serine, threonine and tyrosine residues (Humphrey et al., 2015). This modification impacts the structure and function of proteins and determines their fate in terms of signaling, trafficking as well as metabolism; thus playing an important part in regulating the normal physiological processes (Ravid and Hochstrasser, 2008). Protein phosphorylation is one of the most predominant PTMs that drives enormous cellular cascades in living cells. The phosphorylation of proteins is reversible and very specific. These events of phosphorylation and dephosphorylation are catalyzed by diverse kinases. A variety of kinases like Akt, Erk, and PKA. GSK3β and Cdks have been found to be overexpressed with enhanced activity accompanied by a significant drop in phosphatases activity in AD patients (Alquezar et al., 2021). Accumulating evidence report that various proteins on altered phosphorylation in these neuro disorders drive the cell death signaling cascades (Suprun, 2019).

Tau phosphorylation

Tau is involved in the stabilization of microtubules, as mentioned earlier. Six different isoforms of tau are usually expressed in normal mature human brain which are found to be hyperphosphorylation in AD brains. These six isoforms of tau protein with varied amino acid chain length (331 to 441) emanate from alternative splicing of a single gene. Tau protein has different domains like N terminal projection domain ranging from 1 to 165 amino acids, proline rich domain from 166 to 242, microtubule binding region (MTBR) starting from 243 to 367 as well as carboxy terminal domain 368–441. Tau proteins bear 85 phosphorylation sites; with nearly half of them found to undergo phosphorylation and the majority of these phosphorylated stretches are found in proline rich domain of tau protein, flanking microtubule binding region (Goedert et al., 1989; Hanger et al., 2009). These phosphorylation events and isoform expression are developmentally regulated and it determines the complexity of embryonic cytoskeleton plasticity (Hanger et al., 2007). However, any unusual alterations in its structural conformation or in phosphorylation events impact its binding affinity with microtubule. Tau phosphorylation is residue specific and is mediated by different types of kinases. These kinases are proline rich domain specific kinases like GSK-3, Cdk5, and AMPK, non-proline directed phosphorylating kinases as well as Fyn kinases (Iqbal et al., 2016). Phosphorylation of tau protein by GSK3β at residues other than that of microtubule binding region like, thr231 pro232, and s214 has been found to impede its association with the microtubule thus affecting its anterograde transport (Figure 4). This residue specific phosphorylation leads to the induction of some conformational alterations which in turn lead to hyperphosphorylation of tau protein. It has been found that phosphorylation of Ser 404 accommodated by C-terminal domain alters the tau conformation (Luna-Munoz et al., 2007). Although GSK3B has been found to phosphorylate 36 residues of tau protein, however, preferable sites spotted by 2D phosphor-peptide mapping include Ser199, Thr231 as well as Ser413, respectively. Besides aforementioned mapping, monoclonal antibody technology has been applied to spot the phosphorylation sites that play a role in AD pathology, and it has been found that phosphorylation at specific motifs like Thr212/Ser214 and Thr231/Ser235 are exclusively seen in PHF (Ebneth et al., 1998; Despres et al., 2017). Interestingly phosphorylation of tau proteins at ser293 and ser305 neutralizes its ability to form aggregates without affecting tubulin polymerization. GSK3β like other kinases recognizes primed target proteins as it has been noted that Thr231 residue of tau proteins needs to be primed by other kinases like Cdk5 which is followed by GSK3b mediated phosphorylation. This phosphorylation of tau protein, in turn, impacts its binding ability with the microtubules thus hampering their polymerization and other neuronal functions (Stoothoff and Johnson, 2005). Cdk5 another proline region-specific kinase involved in hyperphosphorylation of tau hampers the ability of tau protein to bind and stabilize microtubules leading to the disruption of axonal transport and neuronal death-an important contributor to the pathology of neurodegenerative diseases like AD (Piedrahita et al., 2010). Growing evidences report that dephosphorylated tau protects nuclear DNA from heat damage and other kinds of oxidative stress insults however tau in hyperphosphorylated form is believed to halt protective functionalities associated with non-phosphorylated forms in neuronal entities (Sultan et al., 2011). Cdk5 isoform is expressed in the brain, unlike cell cycle-related Cdks serine/threonine kinase, shows affinity toward the proline rich domain and phosphorylates some preferable residues like Ser202, Thr205, Ser235, and Ser404; which are found to be essential in regulating Tau-Mt binding. Cdk5 is activated by neuron specific p35 and p39 proteins-which are not considered to be cyclins. Thus, Cdk5 mostly acts in neural cells and is activated by binding to neuronally enriched activators, p35 and p39, to display its functions predominantly in post-mitotic neurons. While the defect of Cdk5 is disparaging to the CNS, its hyperactivation is also lethal to neurons. Some studies have also unraveled the various roles of cdk5 in neuronal remodeling as well as modulation of synaptic transmission (Fleming and Johnson, 1995; Cruz et al., 2003). Fyn, a tyrosine kinase, phosphorylates tyr18 residue and has been reported to precede the deposition of NFT as well as PHF associated with AD pathology (Lee et al., 2004). Exhaustive research has been carried out and it has been observed that hyperphosphorylation of tau protein makes it susceptible to aggregation and leads to the formation of tau assembly in vitro conditions whereas dephosphorylation events reverse its assembly to normal levels as well as stabilizes microtubules back. Coordinated interactions of kinase as well as phosphatases have been seen to maintain the phosphorylation status of tau protein and imbalance in such interplay usually drives its aggregations associated with several tauopathies. Various in vitro studies have been carried out which unraveled the involvement of specific phosphatases involved in the regulation of phosphorylation in AD. It has been found that PP1, PP2A as well as PP5 are residue specific and dephosphorylates the tau protein at particular residues like ser199, ser20, thr212, and ser409 respectively, thus maintaining the balance between kinase and phosphatase action (Liu et al., 2005). These phosphates also drive the positive feedback cycles by regulating the ERK/MAPK signaling cascade that otherwise activates the GSK3β which progresses the aggregation of tau proteins. Among these phosphates PP2A is most extensively studied as it regulates about 70% of tau dephosphorylation in the human brain. Besides phosphorylation, tau proteins undergo other post translational modifications like acylation and glycosylation playing a role in standard microtubule dynamics (Qian et al., 2010). Emerging evidences suggest that overexpression of GSK3β as well as other kinases like Cdk5 plays a part in the progression of these neurodegenerative disorders like AD thus gaining a special interest in treating these disorders by employing therapeutic intervention in the form of specific inhibitors which can inactivate these kinases. Lithium-One of the most commonly used GSK3β inhibitor that inactivates the gsk3b by enhancing its ser-9 inhibitory phosphorylation which acts as a pseudo substrate and prevents its activity (Zhang et al., 2003). It has been reported that the application of lithium treatment in some experimental murine models that are overexpressing human APP, showed some encouraging results in retarding the neuropathology and cognitive impairments (Hu et al., 2009; Undurraga et al., 2019). Lithium is the only GSK-3β inhibitor that has been in clinical use for a significant time. However, we know that lithium lacks target specificity, and shows adverse side effects and high toxicity. Although two molecules AZD-1080 (AstraZeneca) and NP-12/Tideglusib (Noscria) reached the clinic in 2006, AZD-1080 was later on abandoned due to its nephrotoxicity as observed in phase I clinical trial while as NP-12 is currently in phase IIb trials for Alzheimer’s disease and paralysis supranuclear palsy. Meanwhile presently, an increasing number of GSK-3β inhibitors are being tested in preclinical models, and it is anticipated that some of the potent inhibitors will enter clinical trials (Eldar-Finkelman and Martinez, 2011). Recent developments in the field of small-molecule inhibitors of CDKs have led to several compounds with anticancer potencies both in vitro and in vivo and models of cancer. However, the specificity of the inhibitors, which inhibit close isoforms, is not fully achieved yet, especially for CDK5, which is involved in neurodegenerative diseases (Łukasik et al., 2021). Other specific inhibitors have been developed with improved therapeutic effects, some of which are non-ATP competitive inhibitors that are selective and significantly less toxic than others like L803-mts as well as TDZD-8, VP0.7 (Kaidanovich-Beilin et al., 2004; Kaidanovich-Beilin and Eldar-Finkelman, 2006). Other conventional ATP competitive inhibitors include paullones, indirubin, SB415286 and SB216763 as well as AR-A014418 respectively (Leost et al., 2000; Bhat et al., 2007). Tau phosphorylation as well as amyloid beta deposition is impeded by treating the transgenic mouse models that are overexpressing APP, as well as reducing the memory weakening in the Morris water maze (Serenó et al., 2009; Ly et al., 2012). A recent finding suggests that selective GSK3 inhibitor SAR502250 is effective in contributing toward neuroprotection as well as diminish behavioral impairments in rodent models with neuropsychiatric abnormalities. Treatment of P301L human transgenic mice with this inhibitor was seen to reduce the tau phosphorylation thus impairs the formation of tau aggregates. Besides implications of specific inhibitors, genetic knockdowns of GSK isoforms have been also shown to recover cognitive abnormalities associated with various murine models. So these findings suggest that intervention of these kinase inhibitors can possibly act as disease modifying tactics to encounter AD related conditions (Griebel et al., 2019).

FIGURE 4

Figure 4. Displaying how the altered post-translational modifications (PTM) leads to Alzheimer’s pathology-based on the literature surveyed GSK3β dependent hyperphosphorylation of tau proteins results in accumulation of NFT’S and deposition of Aβ plaques–hallmarks of Alzheimer’s disease whereas O-linked glycosylation of tau proteins hampers its aggregation thus promoting normal polymerization processes.

Acetylation

Alzheimer’s disease (AD), also known as a protein misfolding disease, is a degenerative and incurable terminal disease of the central Nervous system (CNS) characterized by the presence of two main types of protein aggregates that include amyloid plaques and NFTs. Both genetic and non-genetic (environmental) factors are involved in the development of AD (Singh and Li, 2012; Tönnies and Trushina, 2017). However, the exact gene-environment interactions involved in the development of AD have not been delineated yet. Epigenetic changes are involved in integrating genetic and environmental interactions. These epigenetic processes are thus considered heritable changes in gene expression without causing any change in the coding sequence of genes. Most common epigenetic alterations reported that impact phenotypic outcomes include histone modifications like acetylation, phosphorylation, methylation, ubiquitination, ADP ribosylation, and SUMOylation; DNA methylation and non-coding RNA (Miller and Grant, 2013). These epigenetic changes regulate gene expression by altering the chromatin structure thereby increasing access to transcription factors (Venkatesh and Workman, 2015). The histone modifications involve acetylation and deacetylation of histone proteins which are the chief protein components of chromatin in the form of histone octamers. Each histone octamer consists of four core histones which include H2A, H2B, H3, and H4 (Shahbazian and Grunstein, 2007). These positively charged histone octamers wrap around negatively charged DNA to form nucleosomes-the basic components of chromatin structure. Acetylation and deacetylation of these histones define the chromatin configuration. Acetylation at the N-terminal tails of H3 and H4 histones neutralizes their positive charge thereby reducing the binding of histone to DNA. Acetylation of core histones, considered as the markers of an open configuration of chromatin, opens up the chromatin to facilitate gene transcription (Struhl, 1998). On the other hand, deacetylation does the opposite. Thus, we can say that histone acetylation promotes transcriptional activation, while as histone deacetylation leads to transcriptional repression of genes. These histone modifications regulate critical cellular processes that include cell proliferation, differentiation, apoptosis, inflammation, neuronal plasticity, and metabolic reprogramming (Thiel et al., 2004). During the process of histone acetylation, Histone Acetyltransferases (HATs) transfer an acetyl group from acetyl coenzyme A to the lysine residues present at the N-terminal domains of core histones. This acetylation neutralizes the positive charge in histones and thus reduces affinity between histones and negatively charged phosphates in DNA. Therefore, it opens up chromatin to promote the transcriptional activity of genes (Bannister and Kouzarides, 2011). In contrast to this, histone deacetylase (HDAC) removes the acetyl groups from histones which results in silencing of gene expression. Thus, both histone acetyl transferases (HATs) and histone deacetylases (HDACs) play an important role in chromatin remodeling (Kuo and Allis, 1998). HATs are broadly divided into two classes based on their subcellular localization: A-type HATs, and the B-type HATs which are seen in the nucleus and cytoplasm respectively (Mersfelder, 2008). A-type HATs are further divided into three subclasses based on their structural homology: (1) GNAT family represented by Gnc5, PCAF, and ELP3; (2) MYST family containing Tip60, MOZ/MYST3, MORF/MYST4, HBO1/MYST2, and HMOF/MYST1; and (3) p300/CBP family containing p300 and CBP. Multiple studies have been conducted to investigate the role of these HATS in the etiology of AD (Lu et al., 2015; Li et al., 2021). HAT activity of Tip60 was shown to regulate the expression of genes that are related to behavior, learning, memory, and neuronal apoptosis in Drosophila (Xu et al., 2014). Similarly, HAT activity of CBP and p300 is related to long-term memory and neuronal survival. An interesting study was conducted in behavior-trained rats where hyperacetylated H2B/H4 in the promoters of the synaptic-plasticity-related genes was observed upon expression of CBP/p300 and PCAF (Chatterjee et al., 2013). Furthermore, AD pathological contexts also show a critical CBP/p300 loss with histone H3 deacetylation (Rouaux et al., 2003). A genome-wide study was conducted to examine the histone H3 acetylation pattern in the entorhinal cortex of AD patient samples and compared with the control subjects using chromatin immunoprecipitation and highly parallel sequencing (Marzi et al., 2018; MacBean et al., 2020). Genes involved in the progression of AD like amyloid-β and tau showed highly enriched acetylated peaks. Ramamurthy E. et al. carried out cell type-specific histone acetylation pattern analysis of AD patients and controls and observed differential acetylation peaks in the early onset risk genes (APP, PSEN1, PSEN2, and BACE1), and late onset genes (BIN1, PICALM, CLU, ADAM10, ADAMTS4, SORL1, and FERMT2) associated with the pathogenesis of AD (Marzi et al., 2018; Ramamurthy et al., 2020).

The histone deacetylases are also classified into four groups based on their homology to yeast enzymes: Class I HDACs consist of HDACs 1, 2, 3, and 8; Class II HDACs which are further divided into two subclasses, class IIa including HDACs 4, 5, 7, 9, and class IIb HDACs 6, 10; Class III HDACs which include SirT1-7; and class IV HDAC that has a single member-HDAC11 (Seto and Yoshida, 2014). Although class I HDACs are ubiquitously expressed, in comparison to HDAC1, HDAC2 and –3 show the highest expression levels in brain regions associated with memory and learning, such as the amygdala, hippocampus, and cortical areas (Volmar and Wahlestedt, 2015). The subcellular localization and expression levels of individual HDAC isoforms differ in different cell types during various stages of AD progression. HDAC2 is reported to negatively regulate memory and synaptic plasticity (Guan et al., 2009). The mice overexpressing HDAC2 showed hypoacetylation of histone H4 on their K12 and K5 residues. These mice also showed memory impairment and decreased number of synapses (Kumar et al., 2005). Since HDAC2 shows high levels of expression in the post-mortem brain samples of AD patients. HDAC2 downregulation by using short-hairpin-RNA restored the memory impairment and synaptic plasticity in CK-p25 mice indicating the critical nature of HDAC in memory formation and synaptic plasticity (Gräff et al., 2012). In another study, HDAC3 was shown to be critical for regulating synaptic plasticity in a single neuron or neuronal populations. Some established human neural cell culture models with familial AD (FAD) mutations showed a significant increase in HDAC4 levels in response to Aβ deposition in this cell model (Citron, 2010). Targeting HDAC4 by the selective inhibitor TasQ rescued the expression of genes involved in regulating neuronal memory/synaptic plasticity (Mielcarek et al., 2015). While high levels of HDAC6 protein were seen in the cortices and hippocampi of AD post mortem brain samples, reducing endogenous levels of HDAC6 were reported to restore learning and memory ability in the mouse model of AD. This happens partly because HDAC6 is shown to significantly decrease tau aggregation and promote tau clearance via acetylation (Fan et al., 2018). Thus, several studies have demonstrated that abnormal acetylation of core histones is involved in the etiology of AD. In addition to histones, altered acetylation of non-histone proteins which include NF-κb, p53, alpha tubulin and tau have also been reported in the pathogenesis of AD. Tau acetylation is mediated by p300 and CBP histone acetyl transferases at different residues. Acetylation of tau reduces its solubility and thus affects its intrinsic propensity to aggregate. Intracellular tau acetylated at Lys280, preferably by CBP, is seen during all stages of AD disease. Tau acetylation is known to suppress the degradation of phosphorylated tau (Chen et al., 2001; Park et al., 2013). Moreover, both acetylated and hyperphosphorylated-tau were reported to show similar spatial distribution pattern. Conversely, HDAC6 activity promotes deacetylation tau, which then contributes to enhanced tau-microtubule interactions and microtubule stability (Carlomagno et al., 2017).

Histone deacetylases (HDAC) inhibitors for the treatment of AD: A growing body of evidence considers HDAC proteins as therapeutic targets for the treatment of AD. HDAC inhibitors may be alternative drugs to potentially protect against the impairment of cognition in AD patients. It is suggested that HDAC inhibitors may be a good alternative to conventional drugs to potentially improve the cognition features in AD patients (Xu et al., 2011). It has been shown that inhibitors targeting HDACs are involved in improving memory and cognition in the mouse model of AD. In AD animal models, HDAC inhibitors show neuroprotective activities, and thus provide a promising strategy for the treatment of AD (Sun et al., 2017). However, care should be taken when using pan-HDAC inhibitors (non-selective HDAC inhibitors) to treat AD because these HDAC inhibitors are poorly selective and often cause some undesired side effects (Cheng et al., 2015; Sun et al., 2017). Thus, evaluating the role of individual HDAC isoforms fin memory, learning and in the pathogenesis of AD becomes all the more important for the discovery and development of more selective HDAC inhibitors. Isoform selective HDAC inhibitors may, however, greatly eliminate side effects and toxicities associated with pan inhibitors and offer improved efficacy (Balasubramanian et al., 2009).

Glycosylation

Glycosylation involves the attachment of specialized forms of sugars called glycans to the target proteins through glycosidic bonding like N and O linkages (Spiro, 2002). Glycans are the sugar moieties linked to protein, lipids or other molecular entities and their structural complexity varies depending on the type of monocarbide core it bears. These glycans regulate the various functionalities associated with the normal functioning of cells like cellular signaling (Varki, 2017). These tissue specific glycosylation patterns have also been reported. Unusual alterations in such modification have implications for different diseases including several neurodegenerative disorders (Abou-Abbass et al., 2016). Nearly 50% of proteins have been observed to undergo such modifications. Glycosylation of proteins usually occurs in the ER and Golgi complex to facilitate the trafficking of proteins to different locations like mitochondria, cytoplasm, plasma membrane, nucleus etc., (Kizuka et al., 2017). This modification is usually catalyzed by enzymes to add glycans to target proteins through glycosidic bonding. Based on the type of glycosidic bonding between sugar moiety and target protein, it is categorized into N-linked and O-linked modifications (Shental-Bechor and Levy, 2008; Haukedal and Freude, 2021). N-linked glycosylation involves the attachment of N-acetyl glucosamine to the asparagine residues of target proteins through β-1N linkages. This modification starts with the synthesis of glycan (14 carbon moiety) from N acetyl glucosamine and mannose sugar, which undergoes further sugar modification, followed by the transfer of modified sugar chain to a particular protein thus acquiring complex form. This whole process is carried out by a specific set of enzymes like mannosidases and glucosidases of ER as well as glycosyltransferases of the Golgi complex (Moremen et al., 2012; Reily et al., 2019). On the other hand, O-linked glycosylation occurs in the several cellular compartments like cytoplasm, nucleus and mitochondria and involves the linking of O-glycans usually in the form of N-acetyl galactosamine or N-acetyl glucosamine to target proteins through Ser/Thr residues without undergoing any kind of alteration in the form of trimming of precursor sugar as is seen in N linked type. Many other sugar modifications are also reported which are carried out by enzymes like glycosyl transferases. These modifications involve the addition of galactose, N acetyl glucosamine, sialic acid etc., to target proteins (Clausen and Bennett, 1996; Akasaka-Manya and Manya, 2020). These sugar modifications usually determine the stereochemistry of target proteins which in turn define the structural organization as well as protein stability (Shental-Bechor and Levy, 2008). In the progression of Alzheimer’s disease (AD), glycosylation is associated with tauopathies. Several proteins like APP and BACE1 are seen to be glycosylated in tauopathy patients (Kizuka et al., 2015). It has been seen that O-glycosylation of tau hampers its aggregation without causing any kind of obstruction in its normal polymerization activity (Mietelska-Porowska et al., 2014). Thus, it has been proposed that glycosylation of tau plays a protective role by blocking tau aggregation. Few O-linked glycosylation sites have been spotted in tau protein at residues which are targets of tau phosphorylation as well. These residues include S400, S238, and S409 (Yuzwa et al., 2011). Unlike O-glycosylation, N-type modifications of tau protein have been observed to affect the subcellular localization of tau protein in AD patients (Alquezar et al., 2021). Transgenic mice models of AD have shown a significant disparity in O-GlcNAcylation and phosphorylation with tau protein being hyperphosphorylated at specific serine residues followed by a drop in O-GlcNAcylation levels (Bourré et al., 2018). Both O-linked glycosylation and phosphorylation of tau protein are well-adjusted in normal conditions and it has been observed that hyperphosphorylated protein shows a decreased glycosylation thus impacting its nuclear localization (Lefebvre et al., 2003). Thus we can say that O-glycosylation competes with phosphorylation and shields tau protein from hyperphosphorylation at particular stretches of serine residues by Protein Kinase A (PKA), therefore playing a protective role in normal brain functions. However, it has been found that N-glycosylation helps tau phosphorylation by hampering dephosphorylation or by activating PKA mediated tau phosphorylation, and thus promotes the progression of pathology associated with Alzheimer’s disease (Liu et al., 2004). Altered glycosylation patterns of many other proteins involved in the progression of neuro disorders like APP have been reported as well. Glycosylated APP has been reported in CSF of patients showing AD pathology (Schedin-Weiss et al., 2014). It has been reported that N-bonded glycan display modulation of amyloid beta production and structural variations in such glycans alters APP transport as well as trafficking. O-linked glycosylation of APP directs it to plasma membranes to promote the processing of APP through non-toxic, non-amyloidogenic pathways, thus lowering the production of toxic amyloid beta peptides (Chun et al., 2015a). N-glycans are also involved in the trafficking and secretion of APP. It has been shown that blocking the activity of mannosidase hampers the production of hybrid and complex forms of N glycan which affects APP transport and other proteins to the synaptic membrane (Bieberich, 2014). Recently site-directed mutagenesis approach has shown that specific O-glycosylation at Thr576, directs its transport toward the plasma membrane and the subsequent endocytosis of APP elevates Aβ levels (Chun et al., 2015b). Treatment of experimental 5XFAD mice with a small molecule inhibitor blocking the glycosylation of gamma secretase lead to reduced production of AB peptides, thus slowing the progression of neuroinflammation followed by recovery in memory impairments (Kim et al., 2013). Patients displaying AD pathology have been found to contain BACE1 post translationally altered with bisecting GlcNAc however blocking this modification using knockout approach slows down APP processing followed by reduced amyloid deposition. Experimental knockout Mgat3-gene mice have been shown to alleviate cognitive abnormalities as well as deposition of amyloid beta aggregates (Elder et al., 2010; Haukedal and Freude, 2021). Besides these enzyme dependent modifications, there are enzyme independent post translational modifications called glypiations which involve the covalent attachment of sugars to lysine residue of target proteins. This alteration usually produces advanced glycation end products (AGES) which are speculated as glycotoxins playing a role in age related diseases (Cho et al., 2007). It has been observed that glycation modifications cause aggregation of the tau proteins by hampering the ubiquitination process required for tau degradation. Moreover. this modification usually reduces the binding affinity of tau protein toward microtubule thus affecting polymerization followed by defective axonal transport and other synaptic functions (Ko et al., 1999).

Fatty acylation

The attachment of long chain fatty acids like palmitate (16 carbon saturated fatty acid) and myristate (14 carbon saturated fatty acid) by amide and thioester linkages respectively is called fatty acylation (Lanyon-Hogg et al., 2017). The mechanism of fatty acylation tunes various cellular processes such as protein-protein interactions, membrane targeting, and intercellular as well as intracellular signaling. Dysregulation in the process of fatty acylation leads to the development of disease conditions including neuronal defects (Wright et al., 2010; Tate et al., 2015). Of all the three lipid modifications viz myristylation, prenylation and palmitoylation; myristoylation and palmitoylation are the most common acylation processes and only palmitoylation is reversible (Resh, 2016).

Palmitoylation

S-Palmitoylation is a vital post-translational modification that is important for the function and trafficking of various synaptic proteins. Palmitoylation reactions are carried out by palmitoyl acyltransferases (PATs) that catalyze the attachment of palmitate (16 carbon) covalently to cysteine residues through thioester bonds (Cho and Park, 2016). Palmitoylation (addition of sulfhydryl group to palmitoyl group) is important for synaptic activity and an increase in palmitoylation contributes to pathogenesis of AD to a large extent (Bhattacharyya et al., 2013). BACE 1 or β-secretase, a 501 amino acid type 1 transmembrane aspartic acid protease, associated with the retroviral aspartic β-secretase protease and pepsin family, leads to APP cleavage in the amyloidogenic pathway generating Aβ including pathogenic Aβ42 (Vassar et al., 2009). S-Palmitoylation of BACE 1 takes place at specific Cys residues viz Cys-474, 478, and 485, out of which Cys 474 is a part of the transmembrane domain. Mutations that change these cysteine residues to alanine cause displacement of BACE1 from the lipid rafts without affecting the processing of APP and produce peptides of amyloid (Vetrivel et al., 2009). S-Palmitoylation of BACE1 and its role in Alzheimer’s disease was studied by developing a gene knock-in transgenic AD mice, where the cysteine residues of S-palmitoylation were changed to alanine residues. The lack of S-Palmitoylation of BACE 1 was observed to reduce the cerebral amyloid burden in AD mice significantly, it also reduced cognitive defects. This suggests that the intrinsic S-palmitoylation of BACE 1 has an impact on the pathogenesis of amyloid and further cognitive decline (Andrew et al., 2017). Palmitoylation targets APP to the lipid rafts and enhances its BACE-1 mediated cleavage which ultimately increases the amyloidogenic processing. Palmitoylation inhibitors impair the processing of APP and α and β (a family of proteolytic enzymes that cleave APP to produce amyloid beta peptides). Acyl Coenzyme A Cholesterol acyltransferase (ACAT) inhibitor, known to redistribute cellular cholesterol, inhibits APP palmitoylation and significantly reduces Aβ generation (Bhattacharyya et al., 2013).

Myristoylation

Myristoylation, is a eukaryotic post and co-translational modification, is the covalent attachment of myristic acid, a 14-carbon saturated fatty acid, to the N-terminal glycine of proteins. Proteins that are destined to be myristoylated begin with the sequence Met-Gly. N-M-T acts on myristoyl coenzyme A and transfers myristate from it to N-terminal glycine to a varied range of substrate proteins. These myristoylated proteins play critical roles in many signaling pathways to mediate protein-protein and protein-membrane interactions, subcellular targeting of proteins etc. Myristoylation is mediated by the enzymes commonly known as N-myristoyltransferases (N-M-T). In vertebrates myristoylation is carried out by NMT1 and NMT2-members of the GCN5 acetyltransferase superfamily, expressed in nearly all tissues and are reported to be involved in the progression and development of various pathological conditions which include Alzheimer’s disease, cancer, epilepsy etc., (Thinon et al., 2014). A key event in AD is the cleavage of APP by β-secretase to generate APP C99, which then undergoes additional cleavages by γ-secretase to produce Aβ40 and Aβ42 peptides (Su et al., 2010). The presenilin-1 (PSEN1) and presenilin-2 (PSEN2) genes encodes the major component of γ secretase responsible for APP cleavage resulting in the subsequent formation of Aβ peptides (Delabio et al., 2014) and altered APP processing is usually seen in AD patients carrying PSEN mutation. It has been shown that calmyrin, a calcium binding myristoylated protein, plays a versatile role in intracellular signaling and is also important in the functioning of presenilin (Stabler et al., 1999). Calmyrin preferentially interacts and colocalizes with PSEN2. The co-expression of calmyrin and PSEN2 in Hela cells were reported to modify the subcellular distribution of these proteins and cause cell death, thus suggesting that these two proteins act in concert in pathways that regulate cell death (Stabler et al., 1999). PSEN2 and calmyrin mutually regulate each other; calmyrin regulates the PSEN2 function when it detects changes in calcium homeostasis, on the other hand, PSEN2 proteins may disrupt calcium homeostasis altering the calcium binding capacity of calmyrin. Also, the overexpression of presenilins causes perturbations in calcium balance (Guo et al., 1996; Keller et al., 1998). Any imbalance in the regulation of calcium could be fatal to the cell because calcium plays a central role in various cellular processes and in apoptosis (McConkey and Orrenius, 1997).

Normally, APP, β-and γ-secretases and phosphatidylinositol 4, 5-bisphosphate (PIP2), which is an signaling lipid moiety for endocytosis, are located on the lipid rafts. Also, It has been shown that endocytotic invagination of the membrane causes smaller lipid rafts to fuse to form larger rafts where APP, β, and γ secretases come together, this combination brings APP, β, and γ secretases in close proximity to one another causing APP cleavage thus, inducing the amyloidogenic pathway in AD (Su et al., 2010). The myristoylated alanine-rich C kinase substrate (MARCKS) usually binds to the membranes to shield PIP2 from taking a part in endocytosis. This process halts endocytosis, thus reducing the Aβ production (van Rheenen et al., 2005). Phosphorylation of MARCKS by protein kinase C (PKC) or its interaction with Ca2 + leads to its release from the membrane into the cytoplasm, thus releasing PIP2 and promoting endocytosis again, and subsequent generation of Aβ40 and Aβ42 peptides in AD (Arbuzova et al., 2002). Thus, MARCKS provides a novel therapeutic option for reducing the generation of Aβ40 and Aβ42 peptides by regulating the pathway of endocytosis.

Ubiquitination

Ubiquitin is a greatly conserved 8.6 kDa regulatory protein composed of 76 amino acids found in almost all tissues of eukaryotes encoded by UBB, UBC, UBA52, and RPS27A genes (Kimura and Tanaka, 2010). Ubiquitination interchangeable with ubiquitylation is the addition of ubiquitin to a substrate protein. Ubiquitination is known to mark proteins for degradation; it can affect their function and alter protein sub-cellular localization as well (Mukhopadhyay and Riezman, 2007). Ubiquitination is regulated by three main enzymes viz (E1) Ubiquitin activating enzymes, (E2) Ubiquitin conjugating enzymes and (E3) Ubiquitin ligase. Ubiquitination can take place by either the addition of a single ubiquitin protein (mono-ubiquitination) or a chain of ubiquitin proteins (Polyubiquitination) (Mukhopadhyay and Riezman, 2007). These modifications generally occur at the side chain of lysine residues or the N-terminal methionine, although lately cysteine, serine and threonine residues have also been recognized as places for ubiquitination (McClellan et al., 2019). The site, length, and attachment of these ubiquitin proteins help to determine the fate and stability of a substrate (Ramesh et al., 2020). As EI, E2, and E3 enzymes help in the attachment of ubiquitin proteins, the deubiquitinases (DUBs) detach ubiquitin proteins from the substrates (Schmidt et al., 2021). Interestingly, Ubiquitin, protein can itself be post-translationally modified with acetylation and phosphorylation for enhanced diversity and regulation. The ubiquitin proteasomal degradation pathway is one of the major routes responsible for the clearance of misfolded proteins to maintain protein homeostasis. Any perturbation of the ubiquitination degradation pathway leads to toxic aggregation of species promoting the onset of various neurodegenerative diseases including Alzheimer’s (Zhang et al., 2017). AD is mainly caused by the unusual accumulation of misfolded proteins and peptides which result in the formation of amyloid plaques and NFTs, respectively. APP, BACE1 and tau proteins are the major targets of abnormal modification by ubiquitination (Perluigi et al., 2016). β-secretase/BACE1 leads to APP cleavage in the amyloidogenic pathway generating Aβ. The therapeutic inhibition/regulation of β-secretase would therefore reduce the production of all forms of beta-amyloid including the pathogenic Aβ42 (Vassar et al., 2009). The regulation of BACE1 level is done by the ubiquitination and proteasome degradation system. Tau is a protein is also rich in lys residues thus has high susceptibility toward ubiquitination. The central role of tau ubiquitination is to regulate tau clearance by proteasomal or lysosomal autophagy system (Gonzalez-Santamarta et al., 2020).

Further, the presenilin (PSEN) proteins are known to play an essential role in AD pathogenesis by mediating the intramembranous cleavage of APP generating (Aβ) (Oikawa and Walter, 2019). In order to sort APP into the endosome and allow their processing by PSEN, ubiquitination of its lysine residues present in its cytosolic domain is carried out by E3 ligases. These ligases are active in Alzheimer’s and they ubiquitinate at Lys 649/650/651/678 of ACR. Any mutation that changes these lysine residues to arginine hinders the ubiquitination of APP and increases Aβ40 levels (Williamson et al., 2017; Figure 5). Apart from this, Lys 203 and Lys 382 of BACE1 are also important ubiquitination sites for degradation. Mutations at these sites also disrupt the degradation of BACE1, thus increasing the production of Aβ (Wang et al., 2012). BACE1 is ubiquitinated by an E3 ligase known as FbX2 via trp280 which causes it to degrade through the proteasome pathway. In turn, the expression level of FbX2 gets affected by PGC-1α [Peroxisome proliferator-activated receptor gamma (PPARγ) coactivator-1α] which is known to promote the degradation of BACE 1 through the ubiquitin degradation system (Ramesh et al., 2020). The AD brain has altered expression levels of both FbX2 and PGC-1α and any supplementation of FbX2 externally reduces the levels of BACE1 and also improves synaptic function (Gong et al., 2010). This suggests that FbX2 has a role in the reduction of Aβ levels.

FIGURE 5

Figure 5. Ubiquitination in Alzheimer’s disease. Ubiquitination of APP by E3 ligase (Stub1) targets it to endosomal degradation. Mutations at lysine residues inhibit the ubiquitination and endosomal degradation of APP increasing the amyloid burden.

The ubiquitination of tau is also an important factor to study AD pathology. NFTs and paired helical filaments (PHFs) which were derived from the Alzheimer’s affected brain at an early stage, depicted that tau is hyperphosphorylated and ubiquitinated at lys-6,11, and 48. These residues thus have a significant role in AD pathogenesis. While lys48 linked polyubiquitination targets tau to proteasomal degradation, lys6 linked polyubiquitination prevents its degradation and thus hinders the clearance of PHFs (Mayeux and Stern, 2012). As already known that dUbs are the species that mediate deubiquitination, the only dUb that has been reported to target tau is the Otub1, a cysteine protease. Otub1 is reported to prevent the degradation of tau by removing Lys48 polyubiquitin chains from the endogenous tau. This removal of the Lys 48 polyubiquitin chain prevents degradation of tau in primary neurons derived from transgenic mouse models, which suggests that Otub 1 has a necessary role in regulating tau ubiquitination (Juang et al., 2012).

SUMOylation

SUMOylation, a reversible post-translational protein modification, occurs by the binding of an 11KDa, Small Ubiquitin-like Modifier (SUMO) peptide to the lysine residues of target proteins. SUMOylation helps in the normal functioning of proteins by regulating the transactivation of transcription factors, localization of proteins and protein-protein interactions to subcellular regions (Zhang and Sarge, 2008; Feligioni et al., 2015). Similar to the ubiquitination pathway, the SUMOylation process also requires a SUMO-EI activating enzyme, a SUMO-E2 conjugating enzyme and a SUMO-E3 ligase to complete the cycle. Various SUMO paralogues (SUMO-1,2,3,4, and 5) get expressed in a tissue specific manner. The subtypes SUMO2 and SUMO3 share sequence homology of around 95% therefore, they are more commonly called SUMO2/3. SUMO1 and SUMO2/3 are predominantly expressed in brains, SUMO4 in lymph nodes, spleen and kidney while SUMO5 is expressed in the testis (Liang et al., 2016). In AD patients, the expression of SUMO-related proteins are altered, for example the post-mortem brain sections taken from Alzheimer’s patients showed enhanced SUMO3 labeling in the hippocampal region (learning and memory) (Li et al., 2003). SENP3 (a SUMO-specific proteases 3), which takes part in the maturation of native SUMO as well as de-SUMOylation process has been reported to get down-regulated in the inferior parietal lobes of sporadic Alzheimer’s patients (Weeraratna et al., 2007). In addition, the proteins like tau, AβPP, GSK3β, BACE1, and JNK which are involved in AD are SUMO targets (Feligioni and Nisticò, 2013). As already known the abnormal intracellular accumulation is an important hallmark in the progression of AD and is an important target for SUMOylation studies. SUMO1 modification of tau happens on K340, through which tau binds with microtubules (Dorval and Fraser, 2006). SUMOylation and phosphorylation of tau are known to stimulate each other reciprocally. Increased SUMOylation enhances phosphorylation and vice-versa. The SUMOylated/Phosphorylated tau does not bind to tubulin thus making it unable to promote microtubule assembly, and it also removes normal tau from the microtubule assembly, which therefore serves as a template for the transition of normal tau into a misfolded protein (Luo H.B. et al., 2014). SUMOylation of tau also leads to increased formation of NFTs by either competing with ubiquitination or by enhancing the aggregation of tau (Luo Y. et al., 2014).

In APP processing, SUMOylation helps in its trafficking, its modulation and finally in its amyloidogenic processing. Both SUMO1 and SUMO2, SUMOylates APP in vitro on lysines 587 and 595 which reduces Aβ levels in Hela cells overexpressing APP (Martins et al., 2016). Apart from tau and APP, BACE 1 SUMOylation also has a significant role to play in AD pathogenesis. BACE 1, cleaves APP during late or early endosome for Aβ generation. SUMOylation of BACE1 at Lys 501, increases the stability and enhances its protease activity resulting in the processing of APP and ultimately excessive Aβ production. Mutation at this SUMOylation site (lys501) causes BACE1 to degrade which confirms that lys501 is important in stabilizing BACE1 upon SUMOylation (Ramesh et al., 2020; Figure 6).

FIGURE 6

Figure 6. SUMOylation of BACE1 and HDAC. SUMOylation at Lys 501 enhances the activity of BACE1 which enhances APP cleavage and increases amyloid burden. Any mutation in the BACE 1 SUMOylation site decreases the amyloid burden. SUMOylation of HDAC at Lys 444 and Lys 476 also decreases the amyloid burden.

Histone deacetylases play critical roles in the modulation of various cellular processes like chromatin remodeling, DNA repair and transcription (Seto and Yoshida, 2014). SUMOylation of HDACs at lys444 and lys476 decrease the amyloid burden (Figure 5). HDACs particularly HDAC1 maintains genomic integrity in cultured neurons and the mouse brain (Pao et al., 2020). Co-localization studies done in vivo and in vitro, have revealed that the SUMOylation of HDAC1 in the hippocampal CA2 region gets increased in the presence of PIAS1(Protein inhibitor of STAT1). HDAC1 SUMOylation also gets enhanced when Aβ is administered directly in the rat hippocampus (Tao et al., 2017). Furthermore, it has been reported that the Corticotropin Releasing Factor (CRF), Insulin like Growth Factor (IGF-1) and Brain Derived Neurotropic Factor (BDNF) increased the SUMOylation in the CA2 region of HDAC1 of the rat brain. SUMOylation of HDAC1 results in the suppression of HDAC1 and CREB (Cyclic AMP Responsive Element Binding). CREB then binds to the region of the promoter of Mcl-2 (a family of proteins having a role in apoptosis) and enhances its expression. HDAC1 SUMOylation promotes cellular apoptosis, enhances the amyloid burden and relieves memory and synaptic deficits in PSEN/APP mice (Tao et al., 2017).

Deamidation

Deamidation is a spontaneous and non-enzymatic post translational modification which takes place at the side chains of asparagine and glutamine (Dunkelberger et al., 2012). Protein and peptides can undergo deamidation of glutaminyl (Gln) and asparaginyl (Asn) to produce glutamyl and aspartyl residues which cause changes in the structure of the protein because of the addition of negative charge. It influences protein stability, structure, folding, and aggregation. Studies done in vivo and in vitro have shown that deamidation rates are dependent upon the pH, primary sequence, and three dimensional structure of the protein, buffer ions, ionic strength, and temperature etc., (Robinson and Robinson, 2001). Although deamidation of proteins has been found to be involved in the process of amyloid formation, however, the role of deamidation in the formation of Alzheimer’s plaques is still not very well understood One hypothesis is that deamidation can contribute to the development of plaque through the isomerization of Asp to iso-Asp that might prevent the damaged peptides to degrade properly (Dunkelberger et al., 2012). As an example, the Tottori Japanese mutation (Asn-7) and the Lowa mutation (Asn-23) are two common Aβ mutations that have been found to deaminate to iso-Asp in AD patients (Wakutani et al., 2004). Under physiological conditions, the process of deamidation takes place through the formation of a 5-membered succinimide ring (intermediate) facilitated by the protein L-isoaspartate-O-methyltransferase (PIMT), which can restore iso-aspartate to succinimide by transferring methyl from S-adenosyl-methionine (SAM) to the side chain of iso-Asp. These 5-membered rings then hydrolyze into aspartic or iso-aspartic acid (from asparagine) or glutamic or iso-glutamic acid (from glutamine) (Dunkelberger et al., 2012). Deamidation produces L-forms of the products, but they also have the potential to racemize to D-forms through the succinimide intermediate. The ratio of normal to iso-products is 1:3 (Dunkelberger et al., 2012). This isomerization increases the length of the backbone by a CH2 group resulting in the addition of a rotable bond in the backbone of the peptide (Dunkelberger et al., 2012) which therefore, causes serious structural changes leading to the augmentation of Alzheimer’s pathogenesis (Roher et al., 1993). It has been shown that different Aβ biochemical pools have different amounts of N-terminus Isomerization. The membrane fractions and insoluble plaques in AD brains have nearly 85% isomerized Aβ_1–15, whereas the soluble and vesicular portions have lower isomerization percentage [42 (Bronisz et al., 2014)]. Moreover, on deamidation some otherwise non-amyloidogenic proteins have been reported to convert to amyloidogenic which also leads to Alzheimer’s disease (Nilsson et al., 2002).

Oxidative/nitrosative stress

The imbalance between the creation of reactive oxygen/nitrogen species (ROS/RNS) and the ability of the cell’s antioxidant defense to neutralize them is known as oxidative stress. The brain requires a lot of oxygen to function correctly and is highly vulnerable to the action of ROS. Furthermore, the brain is abundant in polyunsaturated fatty acids (PUFAs) that are at risk of peroxidation or free radical attack. Moreover, there is a high quantity of iron, a powerful ROS catalyst, and other antioxidant molecules present in the brain. The etiology of several neurodegenerative disorders, including Alzheimer’s disease, has been linked to an increase in oxidative stress. The increase of Aβ peptide and hyperphosphorylated tau protein in the brain during the progression of Alzheimer’s disease has been suggested to have significant pro-oxidant effects, either directly or indirectly. Through activation of NADPH oxidase and inducible nitric oxide synthase (iNOS), amyloid-β could induce reactive oxygen species (ROS) production from cortical neurons, as a result, superoxide anion (O2^–) and nitric oxide are formed, which leads to the production of hydrogen peroxide (H₂O₂) and peroxynitrite (ONOO) (Medeiros et al., 2007). Amyloid-β disrupts the mitochondrial electron transport by negatively regulating the key enzymes involved in the electron transport chain such as cytochrome C oxidase which leads to the increase in superoxide anion (O2^–) and later on its conversion into hydrogen peroxide (H₂O₂) thus exacerbating oxidative stress (Yan et al., 2013). Aβ induced oxidative stress also leads to the activation of different signaling pathways, for example, p38 a member of mitogen-activated protein kinases (MAPKs) family is activated during Aβ-mediated oxidative stress (Zhu et al., 2000). When compared to control individuals, late AD patients had higher levels of several lipid peroxidation markers such as 4-hydroxyhexanal (HHE), F2-isoprostane, and F4-neuroprostane. Peroxidation of lipids harms mitochondria by impairing respiration by releasing electrophilic aldehydes (Kuhla et al., 2007). Protein oxidation indicators such as protein carbonyls and 3-nitrotyrosine (3-NT) were also shown to be higher in MCI and AD patients (Alzheimer’s Association, 2019). Significant increases in the levels of DNA oxidation marker 8-hydroxy guanosine (8-OH-dG) were seen in CSF of Alzheimer’s patients when compared with control (Lovell et al., 1999). Oxidation of different proteins in the brain alters the function of enzymes responsible for the proper neuron and glial function, for example, Glutamine synthetase and creatine kinases undergo oxidative modifications during oxidative stress that leads to excitotoxicity altering the concentrations of glutamate and decrease in energy metabolism in AD (Moreira et al., 2005). As a result of oxidative stress, Aβ, and tau have been shown to undergo a variety of changes. Tau helps to organize microtubules by actively interacting with newly generated microtubules. Modification of tau by oxidative stress leads to the disruption of microtubule organization in AD patients (Heston and White, 1978). Levels of different metal ions such as Cu²⁺ and Zn²⁺ are tightly regulated for different functions of the brain and also prevent the oxidative stress resulting from the interaction of Fe²⁺ or Cu²⁺ with oxygen to generate free radicals. In AD the homeostasis is disrupted and leads to oxidative stress (Deibel et al., 1996).

In AD patients various stress responses or antioxidant genes are activated during oxidative stress such as heme-oxygenase 1, which degrades the prooxidant heme into antioxidant biliverdin, carbon monoxide and free iron. These antioxidants play central neuro-protective roles in AD (Maines, 2000; Pini et al., 2016) Gene expression of Mn^–, Cu-, and Zn-superoxide dismutase (Mn^– and Cu, Zn-SOD), catalase (CAT), glutathione peroxidase (GSH-Px), and glutathione reductase (GSSG-R) is enhanced (Aksenov et al., 1998). Superoxide dismutase (SOD) is an enzyme that catalyzes the conversion of superoxide radicals to H2O2 and oxygen (O2) as part of the body’s initial defense against ROS (Balmuş et al., 2017). In both MCI and AD patients, serum SOD activity was lower than in controls. GSH reacts with oxidized products or ROS either catalyzed by glutathione peroxidase (GPx) or on its own or leads to the formation of glutathione disulphide (GSSG). Glutathione reductase can then convert the GSSG back to reduced GSH (GR). According to various human brain studies, damaged brain areas of Alzheimer’s patients have a decreased ratio of reduced to oxidized glutathione (GSH/GSSG) (Benzi and Moretti, 1995; Li et al., 2015). α-tocopherol (Vitamin E) an endogenous antioxidant protects lipid peroxidation because of its lipophilic nature. Reduced Levels of α-tocopherol were present in the plasma of mild AD patients compared to control (Brigelius-Flohé and Traber, 1999; Baldeiras et al., 2008). Higher vitamin E levels in the blood have also been linked to a lower incidence of Alzheimer’s disease in older people (Mangialasche et al., 2010). Ascorbic acid (vitamin C) is one of the most significant water-soluble antioxidants required for the reactivation of Vitamin E, and its levels in plasma are lower in MCI and AD patients as compared to controls (Rinaldi et al., 2003). Different studies have reported that N-3 PUFA’s is having a strong neuroprotective effect in humans in the early stages of AD development, corresponding to MCI. Enriching brain cells with N-3 PUFA causes a low-level oxidative/nitrosative stress, which will boost antioxidant activities and hence have a neuro-protective impact (Barone et al., 2014). Zhang et al. have recently reported that in both in vitro and in vivo models n-3 PUFAs induces neuroprotective effects through targeting Nrf2 and upregulating heme oxygenase-1 (HO-1) (Zhang et al., 2014).

Therapeutic prospects for the treatment of Alzheimer’s disease

Some of the approaches that can be adopted for the treatment of AD include:

1. Novel exosomes-based therapeutics (NET): Several intriguing properties of exosomes, such as immunological inertness and the natural ability of EVs to transfer cargo between the cells makes them unique natural biological vehicles to cross the biological barriers such as the blood-brain barrier (BBB), which increases their therapeutic potential exponentially for delivering drugs particularly non-coding RNAs across the brain, resulting in silencing of disease-causing genes in the neurological disorders (Familtseva et al., 2019). Further, in mouse studies, it was demonstrated that Neprilysin (NEP) deficient mice showed elevated levels of Aβ, which relates NEP to the degradation of Aβ in the brain (Farris et al., 2003). When MSC-derived exosomes with NEP activity were administered intravenously, it led to reduction in the deposition of Aβ plaques in AD mice, a promising approach in AD therapeutics (Ding et al., 2018). Apart from their role as biomarkers exosomes have also emerged as promising vehicles for pharmaceuticals and they are also reported to play a neuroprotective role in neurodegenerative illnesses and traumatic brain injuries. E.g., exosomes derived from multipluripotent mesenchymal stem cells (MP-MSCs-EXOS), support functional recovery in these illnesses by inhibiting apoptosis and neuroinflammation (Alzheimer et al., 1995). However, the lack of techniques to isolate tissue specific EVs and lack of standard methodology to isolate EVs from different biological fluids are some of the critical challenges that needs to be overcome before utilizing the properties of EVs in treating various challenging diseases. For example, BACE 1 is an important therapeutic target for lowering Aβ levels in AD by specifically silencing BACE1 using small interfering RNAs (siRNAs), significant reduction of Aβ levels were seen (Zhou Y. et al., 2020). Thus, exosome based nanocarrier systems could be employed as effective therapeutic strategies in AD.

2. CRISPR/Cas9 based gene-editing: This approach has demonstrated a great potential for the treatment of AD and other diseases by correcting specific gene sequences (DiCarlo et al., 2017; Schneller et al., 2017; German et al., 2019; Mirza and Karim, 2019; Karimian et al., 2020; Xu et al., 2020; Bhardwaj et al., 2021). In a study using CRISPR/Cas9, gene editing of endogenous APP at the extreme C-terminus inhibited interactions of APP and BAC1 within the endosomes, thereby the most important cleavage event in Aβ generation was avoided in Sporadic AD (Das et al., 2013; Sun et al., 2019). Thus, CRISPR/Cas9 technology could be used to correct increased Aβ production or mutations in APP, PSEN-1, and PSEN-2 genes, which are known to be a causative factor in familial AD, and is a promising tool and has potential for therapeutics in AD. However, further studies are required to establish off-targets and safety of this approach.

3. Nanotherapeutic approaches: Functionalized and tailored nanomaterials have been designed that have the ability to cross the BBB easily and act on the target cells and cellular components like cellular proteins, peptides, and nucleic acids (Tsou et al., 2017; Furtado et al., 2018). Interestingly, nanomaterial-based drugs are considered promising due to their small size and multidimensional therapeutic abilities, and various nano-formulations such as carbon nanotubes, quantum dots, dendrimers, fullerenes, and tailor-made gold nanoparticles help in the targeted delivery of drugs in the targeted cells in AD brain to reduce synaptic impairment (Karthivashan et al., 2018; Farheen et al., 2021; Khan et al., 2021). Interestingly, the amyloid-β-derived peptides prevented in vitro tau aggregation and their inhibitory effect on tau and non-toxic nature points to their therapeutic importance in overcoming AD (Hampel et al., 2015; Kametani and Hasegawa, 2018; Abeysinghe et al., 2020; Farheen et al., 2021). Nanomaterials help in hindering amyloid protein growth and its accumulation due to their highly sensitive molecular detection and identification (Elbassal et al., 2017; Li et al., 2019; Jara-Guajardo et al., 2020; Gorantla et al., 2021). Due to their ability to cross BBB, nanomaterials have been used to identify AD biomarkers, and to study the beta-amyloid protein and tau proteins pathological mechanism (Kametani and Hasegawa, 2018). Another approach in nanotherapeutics is the use of nano-phytomedicine which is the conjugation of nanoparticles and medicinal plants, or their components. The antioxidative, anti-inflammatory, anticholinesterase and, anti-amyloid properties of phytochemicals make them promising therapeutic agents (Bhattacharya et al., 2022). For example, curcumin loaded poly lactic-co-glycolic-acid (PLGA) nanoparticles system has been shown to enhance the action of curcumin and when targeted to the neuroblastoma cell line for the treatment of Alzheimer’s disease they were reported to reduce oxidative damage of the cells. Further, it has been reported that the NPs-Cur delivery system enhances the action of curcumin on several pathways implicated in the pathophysiology of AD by either inhibiting M1-microglial activation or by reducing the expression of apolipoprotein J or clusterin (Chopra et al., 2021). Therefore, nanotechnology-based approaches, with all its advantages already discussed, to target various therapeutic targets in AD including PTMs provides an excellent strategy to manage the progression and decrease the burden of AD.

4. Reactive oxygen species have been shown to be one of the primary drivers in the pathogenesis of AD. Because of the protective effects of phytochemicals against oxidative stress-induced cell apoptosis, they are being explored as potential therapeutic agents for treating or preventing neurodegenerative diseases. Phytochemicals show neuro-protective effects and due to their various effects as anti-inflammatory and antioxidative activities (Palmal et al., 2014). For example, Salidroside, one of the main bioactive ingredients of R. Crenulata, was reported to improve the proliferation and neuronal differentiation of NSCs in the hippocampus of STZ-treated rats, where it acts by scavenging ROS to protect Neural Stem Cells (NSCs) from necrosis and apoptosis (Zhang et al., 2007; Uddin et al., 2021). Another example is Curcumin, which is a polyphenolic natural compound. It has shown its beneficial therapeutic effect in AD and related conditions in various preclinical and clinical studies. The findings from these studies suggested that the curcumin treatment counteracts the deleterious effects of oxidative stress and reverses memory (Walia et al., 2021). Several other phytochemicals have been reported to be involved in slowing down the onset and progression of AD and in improving cognitive functions. However, further research is needed to bring these phytochemicals to a clinical stage, where they can be used as effective antioxidants and/or anti-inflammatory agents for the treatment of AD. Plant derived phytochemicals combined with nanotherapeutics approaches have great potential in targeted therapies for AD and are quite prnset and progressioomising.

5. Another promising therapeutic approach is using antibody-based immunotherapy against Aβ to initiate its clearance or to reduce its neurotoxicity. Recently, Aducanumab, a human monoclonal antibody, when administered intravenously into transgenic mouse models of AD, was shown to selectively target the aggregated forms of Aβ by entering the brain and binding to parenchymal Aβ thereby reducing the soluble and in-soluble forms of Aβ in a dose dependent manner (Qu et al., 2012). Therefore, monoclonal antibody based immuno therapeutics hold a great promise in treating AD, besides other novel therapeutic approaches discussed above.

Future direction

Considering the complex nature of human health and disease, a single gene, protein, glycan or a phosphorylated site may be inadequate as a precise biomarker for diagnosis and for knowing the effective possible cure for any specific disease, so the need of the hour is to establish methods to develop PTM signatures and to develop PTM specific diagnostic and therapeutic interventions for the treatment of AD. Emerging technological approaches like metabolomics, lipidomics, and proteomics hold a great promise and intriguing role in identifying and predicting the progression of neurodegenerative diseases like AD by exploring changes occurring in cells, tissues, and biofluids; structure and function of AD-related proteins, protein-protein interactions (Schumacher-Schuh et al., 2021) and so there is a need to employ these technological approaches for reliable biomarker-based diagnostics and therapeutic interventions. Recently, Huo et al. used targeted multiomics strategy to assess blood and brain samples from different cohorts and reported different serum metabolites that play an important role in predicting cognitive decline in AD patients, as well as other brain metabolites related to neuropathological measurements (Huo et al., 2020). Multiomics profiling analysis of a group of elderly patients with normal cognition, mild cognitive impairments as well as with dementia have unraveled new pathways associated with AD pathology including homeostasis, extracellular matrix signaling as well as immune responses, which enabled researchers to define combination of molecules that could be useful in predicting cognitive impairments as well as omics signatures associated with AD pathology (Clark et al., 2021). Such approaches have made it possible to identify various transcripts and metabolites associated with metabolism of fatty acids and inflammation in AD patients showing disturbances in blood brain barrier and unusual exchange of metabolites. Moreover, new compounds related to AD pathology have been identified by lipidomic analysis in AD patients that include sphingolipids, phospholipids, and ceramides, which have been found to be linked with some neuronal deuteriations like memory impairments, hippocampus volume loss and rapid progression of AD (Han et al., 2011; Mielke et al., 2012). AD is multifactorial disease with varied parameters, of which certain belongs to metabolic changes and some are environmental as well. In order to enhance the specificity of certain biomarkers at varied geographical levels, we need to enhance the proteome analysis of AD patients with accurate and precise detections Untargeted proteome analysis is need of an hour at various AD hit geographical locations to achieve this goal of differential detections and to develop AD therapeutics. A common database generated based on proteome data from plaques or from sera of patients can not only provide an insight of whole protein compositions but also help us to differentiate the proteome of subjects having underlying disease as well giving clear image of changes associated with AD. By using TMT-LC/LC-MS/MS platforms, seven deep proteomic datasets have been developed recently, which identified > 8,000 proteins from 192 subjects (Bai et al., 2020; Higginbotham et al., 2020; Wang Z. et al., 2020; Sathe et al., 2021). These data sets of AD proteome could be used as control data for other geographical locations. After developing the data-sets from various geographical locations, we need to pool the data by high-throughput screening and develop an AI based system which can easily detect the changes in proteins associated with certain factor. So that we can easily make the datasets more reliable and the biomarkers associated with it.

To help identify new biomarkers for AD, molecular profiling which is based on integration of systems biology with high-throughput technology is the best way forward in this direction and these platforms are going to be a valuable tool in AD diagnostics. It is believed that systems biology-based approaches/platforms will help uncover the exact mechanisms involved in the pathogenesis of AD and help understand about triggering factors involved in the onset and progression of the disease (Sevigny et al., 2016). This, in turn, will enable researchers to design disease modifying therapies inhibiting key steps of pathogenesis, and thereby hindering the occurrence and progression of the disease (Hampel et al., 2015; Abeysinghe et al., 2020). Furthermore, it is hoped that recent developments in the identification of biomarkers like miRNAs in exosomes and understanding of circadian clock genes and their dysregulation at different stages will prove to be potential future generation biomarkers, which can revolutionize AD diagnostics. However, more research and validation are needed in this direction.

Conclusion

Biomarkers play a central role in the diagnosis of any disease, but the lack of clinically relevant biomarkers that can provide information about early disease stages as well as its subsequent progression has complicated development of effective treatments for AD. Several candidates as potential biomarkers for early diagnosis of AD are being studied worldwide. We have reviewed the recent literature related to most the advanced technical developments in the identification of biomarkers, like PTM signatures, levels of miRNAs in exosomes and have highlighted the need to understand circadian clock genes and their dysregulations at different stages, which are expected to be potential new generation biomarkers that can revolutionize AD diagnostics. The main hallmarks of AD include accumulation of insoluble proteins primarily composed of amyloid-β plaques and NFTs in the brain. In this review, we have described in detail how aberrant post-translational modifications of AD-related proteins like APP, Aβ, tau, and BACE1 are involved in impairing their normal function resulting in onset and progression of AD. Finally, we also discussed recent developments and therapeutic approaches for AD based on targeted siRNA/miRNA therapeutics, exosome-based drug carriers, nanoparticle-based targeted therapies, CRISPR/Cas9 based gene-editing, monoclonal antibody-based immunotherapies, and phytochemicals which are highly promising interventions that can be employed for the management and treatment of AD in future.

Author contributions

TM and GA conceptualized the idea, developed the contents for this review, and approved the revised final manuscript. IM, MD, and TM prepared the first draft. IM, MA, MK, UM, MG, AB, GD, BA, and AH contributed in writing different sections/sub-section. IM, MA, AB, MK, and UM contributed in the preparation of original figures and tables. TM, GA, MD, IM, MA, MK, and UM contributed in critical revision of the manuscript.

Funding

We are gratefully and acknowledge the technical and financial support from the Ministry of Education and Deanship of Scientific Research (DSR), King Abdulaziz University, Jeddah, Saudi Arabia, under the Institutional Fund Projects Grant No. IFPDP-72-22. Research funding by the University Grants Commission (UGC), New Delhi, India, under BSR Grant No. F.30-357, 2017 (BSR) to TM and Research Fellowship (JRF) by CSIR, New Delhi, India, to IM is gratefully acknowledged.

Acknowledgments

TM acknowledges the help and support received from the University of Kashmir, India.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

AD, Alzheimer’s disease; AGES, Advanced Glycation End Products; APP, Amyloid Precursor Protein; Aβ, Amyloid Beta; BACE, β-Site APP Cleavage Enzyme; BBB, Blood Brain Barrier; BDNF, Brain Derived Neurotropic Factor; BMAL, Brain and muscle ARNT-like; Cas9, CRISPR-associated protein 9; CLOCK, Circadian Locomotor Output Cycles Kaput Protein; CNS, Central Nervous System; CR, Circadian rhythms; CREB, Cyclic AMP Responsive Element Binding; CRF, Corticotropin Releasing Factor; CRISPR, Clustered Regularly Interspaced Short Palindromic Repeats; CRY, Cryptochrome Circadian Regulators; CSF, Cerebrospinal Fluid; ELISA, Enzyme-Linked Immunosorbent Assay; ER, Endoplasmic Reticulum; EV, Extracellular vesicles; EXOs, Exosomes; FAD, Familial Alzheimer’s disease; GSSG, Glutathione Disulphide; HATs, Histone Acetyltransferases; HDACs, Histone Deacetylases; IGF, Insulin like Growth Factor; LOD, Limit of Detection; LP-MS, liquid chromatography-mass spectroscopy; MARCKS, Myristoylated Alanine-Rich C Kinase Substrate; miRNAs, micro RNAs; MP-MSCs-EXOS, Exosomes from Multipluripotent mesenchymal cells; MTBR, Microtubule Binding Region; NCS, Neuronal Stem Cells; NEP, Neprilysin; NET, Novel exosome-based therapeutics; NFTs, Neurofibrillary Tangles; NMT, N-myristoyltransferases; PER, Period Circadian Regulators; PHFs, Paired Helical Filaments; PKA, Protein Kinase A; PSEN, Presenilin; PTMs, Post-Translational Modifications; ROS/RNS, Reactive Oxygen/Nitrogen Species; SCN, Suprachiasmatic Nucleus; SCRD, Sleep and Circadian Rhythm Dysfunction; SiRNAs, Small Interfering RNAs; SUMO, Small Ubiquitin-like Modifier.

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