Abstract
Proper regulation of neurogenesis, the process by which new neurons are generated from neural stem and progenitor cells (NS/PCs), is essential for embryonic brain development and adult brain function. The transcription regulator Patz1 is ubiquitously expressed in early mouse embryos and has a key role in embryonic stem cell maintenance. At later stages, the detection of Patz1 expression mainly in the developing brain suggests a specific involvement of Patz1 in neurogenesis. To address this point, we first got insights in Patz1 expression profile in different brain territories at both embryonic and postnatal stages, evidencing a general decreasing trend with respect to time. Then, we performed in vivo and ex vivo analysis of Patz1-knockout mice, focusing on the ventricular and subventricular zone, where we confirmed Patz1 enrichment through the analysis of public RNA-seq datasets. Both embryos and adults showed a significant reduction in the number of Patz1-null NS/PCs, as well as of their self-renewal capability, compared to controls. Consistently, molecular analysis revealed the downregulation of stemness markers in NS/PCs derived from Patz1-null mice. Overall, these data demonstrate the requirement of Patz1 for NS/PC maintenance and proliferation, suggesting new roles for this key transcription factor specifically in brain development and plasticity, with possible implications for neurodegenerative disorders and glial brain tumors.
Introduction
The Poxviruses and Zinc finger (POZ)/Broad complex, Tramtrack, and Bric à brac (BTB), and AT-hook containing Zinc finger protein 1 (PATZ1), also referred as MAZ related factor (MAZR), Zinc finger Sarcoma gene (ZSG) or Zinc finger factor/protein (ZNF278/Zfp278), is a transcriptional regulator that modulates the expression of several genes, either negatively or positively depending on the cellular context (, ; ). PATZ1 belongs to the POZ and Krüppel (POK) family of transcription factors, which are implicated in many biological processes, including B cell fate determination, cell cycle progression, DNA damage responses and development (gastrulation, limb formation, hematopoietic stem cell fate determination) (; ). Accordingly, Patz1 has been implicated in T cell differentiation (; ; ), cell cycle regulation (), DNA damage response (), and embryonic development (). Noteworthy, a critical role for Patz1 has been described in the maintenance of embryonic stemness through its functional interaction with the pluripotency master genes Nanog and Pou5f1, which are both targets and regulators of Patz1 (). Consistently, mouse embryonic fibroblasts lacking Patz1 show low reprogramming efficiency in induced pluripotent stem cells (iPSCs) ().
In situ hybridization analysis demonstrated that Patz1 gene is actively expressed during early embryogenesis in several districts including the central nervous system, where it mainly localizes in proliferating neural progenitors (NPCs) of the periventricular neocortical neuroepithelium, suggesting a role for Patz1 in neurogenesis (). Indeed, the ventricular and subventricular zone (VZ-SVZ) is located in the wall of the lateral brain ventricles and produces new neurons in both embryonic and postnatal brain of mammals. In the embryonic brain, immature, and neurogenic transient-amplifying NPCs, the intermediate progenitor cells (IPCs), originated from multipotent radial glia cells (RGCs), also known as apical progenitors (APs) in the VZ-SVZ (; ; ; ). The IPCs produce a huge variety of neuronal cell types that migrate toward their final destinations, thus contributing to brain formation and function (). In the adult, neural stem/progenitor cells (NS/PCs) are also present in the SVZ. NSCs activate, upon an injury or inflammatory stimulus, to produce transient-amplifying neural progenitor cells (NPCs) that divide and generate a different type of proliferating progenitors, the neuroblasts (NBs), that eventually differentiate to produce newborn neurons (; ; ).
Genetic inactivation of Patz1 gene in mice results in a partial embryonic lethality and several developmental defects in testes, cardiac outflow tract and brain (; ). The latter defects consist in hypoproliferation of the periventricular tissue, one of the key neurogenic sites, consistently with the idea that Patz1 could play a crucial role in neurogenesis ().
To verify this hypothesis, we first deeply examined Patz1 gene expression in different sub-regions of the embryonic, fetal, juvenile and adult mouse brain, showing a decreasing trend with respect to time, as opposed to a stable expression of Patz1 at neurogenic sites of the adult brain. Then, we analyzed the in vivo incorporation of the DNA intercalant 5′-bromo-2′-deoxyuridine (BrdU) at embryonic stage, and we isolated and ex vivo cultured both embryonic and adult NS/PCs from Patz1-null homozygotes, heterozygotes and wild type mice to perform neurosphere assay and gene expression analysis. All together the results indicate that Patz1 inactivation leads to a drastic impairment in the number and self-renewal capacity of NS/PCs, therefore pointing out to a key role of Patz1 in maintenance and proliferation of NS/PCs.
Materials and Methods
Analysis of Patz1 Transcript Distribution From Publicly Available Datasets
To analyze Patz1 expression levels across development in different cellular populations we took advantage of different publicly available datasets. Normalized fragments per kilobase of exon model per million reads mapped (FPKM) expression values were downloaded from “Mouse RNA-seq time-series of the development of seven major organs” experiment of EMBL-EBI Expression Atlas (; ). The experiment comprises gene expression data (mRNAseq) from different tissues (among them heart, brain, liver, testis, ovary) across several time points from embryonic day 10.5 (E10.5) to postnatal day 63 (P63). Expression data relative to Patz1 in this dataset are represented in the heatmap (A) and in the barplot (B) in Figure 1. Two single cell RNA-seq dataset were also analyzed (©2020 10× Genomics 10K E18 Brain cells; - GSE118953). We downloaded row counts and metadata relative to 10,000 cells from E18 mouse brain from the 10X Chromium website and data relative to the Telley dataset using GSE118953 accession number in the GEO database1. Clustering analysis was performed with R version 4.0.3 (2020-10-10) using Seurat package version 3.2.3 (; ; ). The dataset was normalized using standard SCT normalization pipeline2. A cell cycle score was also assigned to each single cell using the Seurat pipeline but was not used as variable to regress during normalization because considered biologically relevant. We considered the top 60 statistically significant principal components as input for UMAP dimensional reduction, using the DimPlot function. To identify cellular clusters, we used FindClusters function considering 0.2 resolution for both datasets. The robustness of the clustering was validated using an in silico downsampling approach. To annotate cell clusters, top 20 differentially expressed genes (markers) per cluster were considered and the most relevant were plotted using DotPlot function to check cell type specificity. Data relative to 10X-Chromium dataset were shown in Figures 2A–D, whereas data relative to the dataset of were shown in Figures 3A–C. We also analyzed bulk-RNAseq data derived from purified NS/PCs from adult murine SVZ (). The normalized expression matrix of the dataset of was downloaded from GEO database using GSE138243 accession number. Expression data relative to Patz1, Cd9, Slc1a3, Tbr2, Dcxa, and Cd24a genes were reported in the heatmap (scaled data) and in the floating box plot (normalized expression) in Figures 2E,F.
FIGURE 1
FIGURE 2
FIGURE 3
Animals
Patz1-knockout mice were previously described (). C57/BL6 wild type mice were used to collect mouse brains at different embryonic and post-natal stages of development. Mice were maintained under standardized non-barrier conditions in the Laboratory Animal Facility of Istituto dei Tumori di Napoli (Patz1-knockout mice and their wild type controls) and in the Animal Facility of the Institute of Genetics and Biophysics (C57/BL6 wild type mice showed in Figure 1) in Naples, Italy. All studies were conducted in accordance with the Italian regulations for experimentations on animals (prot. no. 576/10 approved by the Italian Ministry of Health on 3 February 2011).
Patz1 Genotype Analysis
Tail pieces from both embryos and adult mice were lysed in tail digestion buffer (50 mM Tris, pH 8.0; 100 mM EDTA, pH 8.0; 100 mM NaCl; 1% SDS) plus proteinase K (0.6 mg/ml) over-night at 55°C. Genomic DNA was extracted by phenol/chloroform/isoamyl alcohol (1:1), precipitated with 95% ethanol and dissolved in TE (Tris/EDTA) buffer, pH 7.5. A set of three primers was used to detect both normal and mutant Patz1 alleles by polymerase chain reactions (PCR), as previously described (). The primers used were: 5′—GCC TTC TTG ACG AGT TCT TC–3′/5′—CCA CAC CAT CAA AGT TGG–3′ for the knockout allele; 5′—AAG CAA GTG GCT TGT GAG–3′/5′—CCA CAC CAT CAA AGT TGG–3′ for the wild type allele.
Brain Dissection
For embryonic brain collection, C57/BL6 mice were crossed. Noon of the day on which the vaginal plug was detected was considered as 0.5 days post coitum (dpc) in the timing of the embryo collection. Timed pregnant females were sacrificed by cervical dislocation and embryos were dissected from decidual tissue in cold PBS. For each embryonic stage two different embryonic litters were analyzed. For each litter, brains from three embryos were dissected into the different territories. Corresponding brain territories of the same litter were pulled together to increase starting material. At each postnatal stage, two mice were sacrificed by cervical dislocation and brains were extracted and then dissected into the different territories. Each postnatal brain territory was analyzed separately.
The dissection was started separating the head from the body using scissors, then, a midline incision along the integument from the neck to the nose was made to expose the skull or its primordium. Any residual tissue was removed using scissors or tweezers. Before to proceed to surgery, all the dissection instruments were disinfected with 70% ethanol. Moreover, the instruments were sterilized with 70% ethanol before the removal of each tissue in order to avoid contaminations.
RNA Extraction and Reverse Transcription–Quantitative Polimerase Chain Reaction (RT-qPCR)
Five hundred microliter of Trizol reagent (Sigma, St. Louis, MO, United States) were added to each sample, except for adult cerebellum and mesencephalon in which 1 ml was added, for subsequent RNA extraction according to the manufacturer’s protocol. Recovered RNA was reverse transcribed using M-MuLV Reverse Transcriptase (Roche Diagnostics). qPCR was performed with SYBR Green PCR Master Mix (Life Technologies) under the following conditions: 10 min at 95°C, followed by 40 cycles (15 s at 95°C and 1 min at 60°C). Each reaction was performed in duplicate in at least three independent experiments. The 2–ΔΔCt method () to calculate the relative expression levels (fold change) was used. Amplification of two housekeeping genes, Glucose-6-Phospate Dehydrogenase (G6PD) and Ribosomal Protein S9 (RPS9) genes, was used to normalize the amount of cDNA. For analysis of brain territories in Figure 1, E11.5 or E14.5 samples have been used alternatively as calibrators to calculate the relative expression. For analysis of neurospheres, both proliferating and differentiated in Figure 6, one of control samples, randomly chosen and different for each independent experiment, was used as calibrator to calculate the ΔΔCt. Sequences for forward (Fw) and reverse (Rv) primers were as follows: Patz1 Fw = 5′-GAG CTT CCC CGA GCT CAT-3′; Patz1 Rv = 5′–CAG ATC TCG ATG ACC GAC CT–3′; Nanog Fw = 5′–GCC TCC AGC AGA TGC AAG–3′; Nanog Rv = 5′-GGT TTT GAA ACC AGG TCT TAA CC-3′; Nestin Fw = 5′—GAG AAG ACA GTG AGG CAG ATG AGT T–3′; Nestin Rv = 5′—GCC TCT GTT CTC CAG CTT GCT–3′; Tubb3 Fw = 5′—GAA TGA CCT GGT GTC CGA GT–3′; Tubb3 Rv = 5′—CCG ATT CCT CGT CAT CAT CT–3′; G6pd Fw = 5′—CAG CGG CAA CTA AAC TCA GA–3′; G6pd Rv = 5′—TTC CCT CAG GAT CCC ACA C—3′; Rps9 Fw = 5′—CTG GAC GAG GGC AAG ATG AAG c—3′; Rps9 Rv = 5′—TGA CGT TGG CGG ATG AGC ACA—3′.
Bromodeoxyuridine Pulse-Labeling and Detection
Heterozygous Patz1-mutant mice were mated and vaginal plug monitored each day to establish the coitum day. At 15.5 days dpc pregnant mice received a single intra-peritoneal injection of 5′-bromo-2′-deoxyuridine (BrdU) (50 mg/kg) and, 2 h later, they were euthanized. One embryo for each genotype was extracted, post-fixed in 4% paraformaldehyde for 24 h and then kept in 70% ethanol at 4°C before to be processed for immunofluorescence analysis. Embryos were then dehydrated through ascending ethanol, washed in Toluene and Toluene-Paraffin 1:1, included in paraffin and then sectioned using a microtome to undergo histological analyses (). For details see elsewhere (). Briefly, cutting angle and thickness have been set, respectively, at 5 and 8 μm. Paraffin sections have been dewaxed in xylene (pre-warmed at 55–65°C) twice for 5 min and then rehydrated through sequential steps in gradually less concentrated ethanol solutions and rinsed in tap water, at the end. Slides have been heated in a 10 mM sodium citrate pH 6.0 in a microwave to expose the antigens (). Tissue sections have been incubated 1 h at R.T. with a solution 1% milk, 10% FBS, 1% BSA, 1X Sodium Azide, 0,5% Tween in PBS 1X and then O.N. at 4°C with a rat-monoclonal BrdU antibody (Novus Biologicals NB500-169) at dilution 1:400. Sections have been rinsed and incubated 1,5 h at R.T. with a Donkey α-rat Alexa Fluor- 488 secondary antibody (Molecular Probes A-21208) at 1:400 dilution, counterstained with Hoechst 1:5,000 and then mounted.
Patz1 Immunological Detection
Sections were dewaxed in xylene, hydrated in graded series of alcohol and subjected to heat-induced antigen retrieval (). After blocking endogenous peroxidase activity, the tissue was incubated for 1 h at R.T. with the blocking solution previous described and then with our previously characterized polyclonal antibody able to recognize both human and mouse Patz1 proteins () at a dilution 1:40 (V/V) O.N. Subsequently, the slices were rinsed and incubated with the biotinylated secondary antibody, at room temperature, for 30 min. The bound antibody complexes were stained for 3–5 min with diaminobenzidine, and slides were then counterstained with hematoxylin (30 s), dehydrated and mounted.
Neurosphere Culture, Proliferation, and Differentiation Assays
Before surgery all the dissection instruments have been disinfected with 70% ethanol. Adult mice or pregnant females were euthanized. SVZ dissection from 4 wild type, 3 Patz1+/– and 2 Patz1–/– adult mice or total forebrain dissection from 6 wild type, 6 Patz1+/– and 2 Patz1–/– 13.5 dpc embryos was carried out under stereoscopic control in ice-cold disodium phosphate buffer solution supplemented with glucose 0.6% (PBSg). The dissected samples were transferred into a new sterile cold PBSg buffer and brought under the hood where they were mechanically dissociated in single cell suspension.
For each sample, cells were counted and plated at the density of 3,000 cells/cm2 in 14–16 ml of serum-free medium comprising 1:1 mixture of DMEM and F12 supplemented with 2 mM glutamax, N2 supplement (1:100), B27 minus Vitamin A (1:50) (Invitrogen), 20 ng/ml EGF (Sigma), 20 ng/ml bFGF (Sigma) and penicillin/streptomycin (1:100), into T75 neurosphere-flasks in a prewarmed culture medium, to obtain a single embryo cell culture. 1 × 105 and all cells recovered from dissection were plated for embryonic and adult neurospheres, respectively. The number of neurospheres/brain were counted under microscope after 4 days in culture for embryonic cells and 7 days for adult ones, and their diameter measured by ImageJ. Only neurospheres > 40 μm in diameter were considered (). Primary neurospheres (P0) were then disaggregated by incubating with TripleExpress dissociation reagent (Invitrogen) for 5 min at room temperature. After the incubation, the dissociation reagent was aspirated, the neurosphere were mechanically dissociated and replated (1 × 105/plate) to form secondary neurospheres (P1). Initial self-renewal activity was evaluated by counting the number of P1 neurospheres/cell seeded ∗ 100.
For differentiation assay, neurospheres at passage 3 were dissociated to obtain single cell suspension, as described above and plated on poly-D-lysine coated multiwell plates at a density of 50,000 cells/cm2. Cells were grown in absence of growth factors for 6 days in a 1:1 mixture of Neurobasal and DMEM/F12 medium supplemented with B27 plus Vitamin A (1:50), 2 mM glutamax (Invitrogen) and penicillin/streptomycin (1:100). Half of the differentiation medium was replaced every other day.
Image Quantification
ImageJ/Fiji software was used to perform image analysis (). To compute the percent of BrdU+ cells (Figure 3F), 10 different images were analyzed per sample by defining the number of BrdU+ cells over Hoecsht+ cells on 5 different regions of interest (ROIs) manually set on VZ/SVZ using Cell Counter ImageJ Plug-in. The lateral ventricle area was computed over 5 different images per sample spanning from anterior to posterior regions, by segmenting Hoecsht signal and automatically defining ROIs over segmentation using ImageJ default threshold algorithm (Figure 3G). BrdU intensity signal per cell was computed by segmenting single positive nuclei of 3 different images per sample using ImageJ MaximalEntropy threshold function and computing the Mean Intensity arbitrary unit (a.u.) score using the Analyze Particle function. Representative quantifications of this analysis are shown in the dot plot in Figure 3H.
To compute the percent of β-III-tubulin+ cells (Figure 6F), 5 different images were analyzed per sample by defining the number of β-III-tubulin+ cells over Hoecsht+ cells using Cell Counter ImageJ Plug-in. NeuroJ Plung-in was used to perform neurite guided tracing and perform number (Figure 6H), length (Figure 6I), and fluorescence score (Figure 6J) analysis of 3–5 neurons per image for at least 3 images per sample.
Statistical Analysis
Pearson correlation test was performed among the Patz1 expression levels detected and the age of the analyzed samples (Figure 1) and between Patz1 and Nanog expression in Patz1+/+ and Patz1+/– adult neurospheres (Supplementary Figure 1). Ordinary one-way analysis of variance (ANOVA) followed by Tukey’s multiple comparisons test was applied for comparison of all the other sets of data. The values analyzed are the average ± SD of at least two biological replicates and three independent experiments. All tests were assessed using GraphPad Prism 7 software, La Jolla (CA), United States. Statistical significance was indicated by ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ****p < 0.0001 vs. wild type control when not differently specified in the figures by linking lines.
Results
Patz1 Is Expressed During Mouse Brain Development and Turns Down in Adult Brain
To get insight into Patz1 expression pattern during embryonic development, we took advantage of the Expression Atlas publicly available dataset containing RNA-seq data from different tissues across multiple timepoints during both embryonic and postnatal development (Figures 1A,B). As shown in Figure 1A, Patz1 expression is frequently higher during embryogenesis than in postnatal and adult stages, with the strongest expression of Patz1 in embryonic brain respect to the other tissues analyzed (heart, liver, ovary, and testis). Interestingly, during brain development, a decreasing trend of Patz1 expression with respect to time, from E10.5 to P63, is quite evident (Figure 1B).
To confirm and expand these findings, we analyzed, by means of qPCR, Patz1 transcript distribution levels in specific mouse brain territories at different time points during both embryonic (11.5, 14.5, and 17.5 dpc) and postnatal (14 days and adults) life. The results are shown in Figure 1C and confirm the existence of a temporal Patz1 expression gradient, with higher levels of expression at early embryonic stages, that decrease during embryogenesis and even more during postnatal (P14) and adult life, when Patz1 expression reaches the minimum measured level. This trend is detectable in the whole brain (Pearson correlation index = −0.6249; p = 0.0014) and also in the specific structures analyzed, as reported in Figures 1C–E. Conversely, there is no preferential spatial distribution at the different embryo and adult stages. Interestingly, looking at the relative expression of Patz1 in the adult, a higher expression level was detected in telencephalic structures (olfactory bulbs, cortex, and hippocampus), in which neurogenesis mainly occurs after birth, respect to the most posterior ones (Figure 1C).
Patz1 Is Enriched in Proliferating Neural Progenitor Cells Inside the SVZ and Appears Involved in Their Maintenance
Given the complex cellular heterogeneity and temporal dynamics of embryonic and adult brain tissue, we took advantage of publicly available single-cell and bulk RNA sequencing datasets to get insight into Patz1 expression level in neural progenitors during brain development. By analyzing the 10× Genomics 10K E18 Brain cells dataset, we found an enrichment of Patz1 expression in early apical radial glia/neural stem cells (RG/NSCs) and intermediate progenitors (IPCs) (Figures 2A–D). We also examined Patz1 expression in a dataset of bulk RNA sequencing from sorted types of progenitors from mouse adult SVZ (), finding that Patz1 was expressed in the entire proliferating lineage with an enrichment in neural progenitor cells (NPCs) and neuroblasts (NBs) (Figures 2E,F). A further analysis, on single-cell RNA sequencing of sorted progenitor cells belonging to presumptive somato-sensory cortex of E12, E13, E14, and E15 mouse embryos (), confirmed an enrichment of Patz1 expression during development in early apical radial glia/neural stem cells (RG/NSCs), mainly at the E12 stage (Figures 3A–C). Accordingly, Patz1 immunodetection at E15.5 showed a strong immunoreactivity in the cortical plate as well as in the VZ/SVZ of wild type embryo (Figure 3D). As expected, no Patz1 immunosignal was detected in corresponding brain sections of null mutants (Figure 3D). All these data point out to a possible function of Patz1 during embryonic neurogenesis. Then, to have a first indication of the impact of Patz1 depletion on proliferating cells in the periventricular area, we examined the in vivo proliferation inside the SVZ of 15.5 dpc Patz1-null and heterozygous mouse embryos, compared to wild type control, using a saturation BrdU (5′-bromo-2′-deoxyuridine) pulse-labeling method (; ) that could label the entire pool of proliferating NS/PCs within a 12 h-period (Figure 3E). BrdU is a thymidine analog that incorporates into dividing cells during DNA synthesis. BrdU-labeling appears weaker and unevenly distributed in the SVZ of Patz1-null and heterozygous mutants compared to control brains. Quantitative analysis indicates a reduction of the number of proliferating cells (Figure 3F) and a significant decrease of BrdU incorporation level (Figure 3H) coupled to an overall reduction of lateral ventricle area (Figure 3G) in both Patz1 mutants compared with control. Interestingly, the heterozygous shows mean values lower than wild type and higher than Patz1 null mutant for all parameters analyzed.
Reduced Proliferative Capacity in Patz1-Knockout-Derived Neurospheres
To effectively measure the number of NS/PCs and their proliferation rate, we performed neurosphere assays on both Patz1 mutant and wild type brains. In this assay NS/PCs derived from SVZ of Patz1–/–, Patz1+/– and wild type adult mice (more than 1 month up to 21 months of age) as well as from 13.5 dpc embryonic telencephalon (from which SVZ arises), were allowed to proliferate in culture at very low density to form spheroid cell aggregates called neurospheres. The number of neurospheres was determined after 4 days in culture for embryonic and 7 days for adult neurospheres (Figures 4A, 5A). Under these conditions, primary neurosphere colonies are derived from single cells and can be used as a good model of the number of in vivo NS/PCs (; ). In agreement with in vivo BrdU labeling data (Figures 3E–H), the number of primary neurospheres (P0) isolated from Patz1–/– embryonic telencephalons was significantly lower than wild type counterparts (mean difference −1208; 95% CI of diff. −2377 to −39.62) (Figures 4B,C). The diameter of each neurosphere, an indirect measure of the ability of cells to grow and proliferate, was also determined, showing a significant reduction in neurospheres derived from Patz1–/– embryos compared to the wild type (mean difference −12,36; 95% CI of diff. −24.48 to −0.2338) (Figure 4D). Furthermore, to assess the initial NS/PC self-renewal capability, primary neurospheres were dissociated into single cells after 4–7 days in culture and 10,000 cells per sample were cultured as above to form secondary neurospheres (P1) that were counted (day 8 and 14 for embryonic and adult neurospheres, respectively). As shown in Figure 4E, we observed a significant reduction (mean difference = −1.787; 95% CI of diff. −3.261 to −0.3126) in the number of P1 neurospheres from Patz1–/– embryos compared to wild type controls, indicating the impairment of the self-renewal ability of Patz1-null NS/PCs. The reduction of the number (mean difference −332.9; 95% CI of diff−561.5 to −104.4), the diameter (mean difference −81.52; 95% CI of diff. −145.8 to −17.26) and the self-renewal capability (mean difference −3.425; 95% CI of diff. −6.053 to −0.7973) of NS/PCs lacking Patz1 was also evident in the SVZ of adult brain (Figure 5). Even though no significant difference was observed in the number and size of neurospheres from the heterozygous Patz1+/– brains, compared to both Patz1–/– and wild type samples, data from both embryonic and adult samples suggest for Patz1+/– heterozygotes an intermediate trend between Patz1-null mutants and wild type controls (Figures 4C,D, 5C,D). Noteworthy, both embryonic and adult Patz1+/– NS/PCs showed a self-renewal capability significantly higher than Patz1-null homozygotes and comparable to wild type (Figures 4E, 5E).
FIGURE 4
FIGURE 5
Overall, these data provide evidence for a role of Patz1 in the maintenance, proliferation and self-renewal capability of NS/PCs at both embryonic and adult stages.
Downregulation of Stem Cell Related Genes and Enhanced Neuronal Differentiation in Patz1-Knockout-Derived Neurospheres
RNA extracted from embryo-derived neurospheres, after at least three passages in culture (Figure 4A), under proliferating conditions, was used to analyze expression of genes characteristic of stemness (Nanog) and neural progenitor (Nestin) phenotype in proliferating neurospheres, or neuronal (Tubb3) cells. Nanog is a DNA binding homeobox transcription factor involved in embryonic stem cell proliferation, renewal, and pluripotency, which is a general marker of stemness; Nestin, neuroepithelial stem cell protein, is an intermediate filament protein that has generally been considered to be a marker of NS/PCs and is crucial for their self-renewal and survival; while Tubb3, coding for β-III-tubulin, correlates with neuronal differentiation (). In agreement with the above data, both Nanog and Nestin genes were significantly downregulated in homozygous Patz1-null NS/PCs with respect to wild type (Figures 6A,B), confirming also at molecular level that Patz1 inactivation strongly affects the stem/progenitor phenotype. Moreover, Patz1-null heterozygous neurospheres also showed a significant downregulation of Nanog and Nestin expression with respect to the control ones. However, Nestin expression levels of Patz1+/– NS/PCs settle in the middle between Patz1–/– and wild type NS/PCs, whereas Nanog expression of Patz1+/– NS/PCs was as low as in the homozygous Patz1-null neurospheres. These results might suggest a significant reduction of the Nestin+ and Nanog+ cells in Patz1-knockout NS/PCs compared to wild type controls. However, according to the role of Patz1 as a positive regulator of Nanog expression in mouse embryonic stem cells (), Patz1 might activate Nanog expression also in NSCs and the reduced levels of Nanog could be partly due to the direct modulation of Nanog promoter by Patz1. Consistently, Patz1 and Nanog gene expression were highly correlated in adult neurospheres as well (Pearson correlation index = 0.9; p = 0.0069) (Supplementary Figure 1).
FIGURE 6
Conversely, the expression of Tubb3 did not change significantly in the three groups (Figure 6C), even though a slight increasing trend was visible among the different genotypes from Patz1+/+ to Patz1–/– proliferating neurospheres, which might suggest an accelerated differentiation into neurons of the Patz1-null neurospheres. To verify this hypothesis, neurospheres were cultured for 6 days in differentiating conditions and neuronal differentiation was confirmed by β-III-tubulin immunodetection (Figure 6D). Tubb3 transcript levels after neurospheres differentiation did not show any significant difference among the different genotypes (Figure 6E), as well as the number of β-III-tubulin+ cells detected (Figure 6F) and the mean fluorescence level per neuron (Figure 6G). However, both number and length of neurites were higher in Patz1–/– than in both Patz1+/– and Patz1+/+ cells (Figures 6H–J), indicating that Patz1-null neurospheres can go toward an enhanced neuronal differentiation compared to control. Consistent with the genotype, Patz1 expression in heterozygous was about half the level of wild type cells, while it was not detected at all in Patz1-null samples (Figure 6K). Interestingly, its expression was lower in differentiated than in proliferating cells, once again supporting a role of Patz1 in counteracting neuronal differentiation.
Discussion
Growing evidences suggest that Patz1 and stemness are closely associated. Patz1 is required for pluripotency maintenance of mouse embryonic stem cells (ESCs), by regulating expression of pluripotency master genes Pou5f1 and Nanog (), and its gene dosage is crucial for an efficient reprogramming of mouse induced pluripotent stem (iPS) cells (). Moreover, during mouse embryonic development, Patz1 gene expression has been detected in actively proliferating neuroblasts of the periventricular and subventricular neocortical neuroepithelium, and Patz1–/– embryos showed anatomical reduction of the SVZ ().
Here, we confirmed and expanded these previous results, revealing a temporal decreasing expression gradient of Patz1 gene during mouse brain development. Indeed, Patz1 transcription levels in the brain decrease during embryogenesis and even more at postnatal stages, reaching the minimum levels in adult mice. In adults, higher Patz1 expression levels correspond to brain structures characterized by still active neurogenesis, such as olfactory bulbs, cortex and hippocampus. The maintenance of high Patz1 expression in the adult hippocampus, a region that is essential for many forms of learning, memory and mood regulation (), suggests that aberrant expression of PATZ1 could contribute to neurological and psychiatric disorders. Indeed, adult-generated neurons and the dynamic regulation of neurogenesis by epigenetic factors are relevant for neuropsychiatric disorders, including depression, addiction, and epilepsy (). Consistently, PATZ1 has been identified as one of the differentially regulated key genes in a form of depression (). Moreover, very recently, PATZ1 has also been associated to Parkinson’s disease, consistent with its possible contribution to neurodegenerative diseases (). However, no studies have so far specifically investigated the role of PATZ1 in NS/PCs.
We now showed an in vivo analysis of BrdU incorporation in embryonic brain of Patz1-null mutant mice, confirming previous observations () and suggesting a different distribution and lowered number of proliferating cells inside the SVZ of Patz1-null mutants compared to wild type embryos. Quantitative and qualitative analysis of neurospheres in culture is extremely helpful in studying both self-renewal and differentiation potential of NS/PCs and dissecting mouse mutant neural phenotype (; ; ). By using this approach on our Patz1-knockout mouse model, we explored the role of Patz1 in self-renewal and proliferation of NS/PCs. Albeit with the limitation of a small number of Patz1–/– samples, due to the high and early embryonic lethality of this genotype in our current mouse colony, the data indicate that Patz1 contributes to proliferation and self-renewal of NS/PCs inside the SVZ, likely playing a role in the early development of the mouse brain, and lately in the maintenance of the adult neurogenic niches. Indeed, evidence for a role of Patz1 in the maintenance and proliferation of NS/PCs was corroborated by impairment of the self-renewal of Patz1-null NS/PCs in both embryonic and adult ex vivo neurosphere cultures derived from telencephalon and SVZ, respectively. Consistent with neurosphere functional data, the gene expression analysis in proliferating neurospheres also suggests that Patz1 inactivation might strongly impair the ability of these NS/PCs to maintain a stemness phenotype. Indeed, the Patz1-null neurospheres express significantly lower levels of stemness and neural progenitor markers, such as Nanog and Nestin, respectively, while the neuronal marker Tubb3 does not seem to be affected, indicating a specific role of Patz1 in their proliferation and self-renewal. These data are consistent with recent results in other cell types, such as rat thyroid cancer stem-like cells, in which Patz1 expression enhances self-renewal ability ().
We also provided a first evidence of a negative role for Patz1 in the differentiation of embryonic neurospheres, showing enhanced neuronal differentiation in Patz1–/– compared to Patz1+/– and Patz1+/+ cells. Moreover, differentiated wild type cells had significantly lower levels of Patz1 than non-differentiated neurospheres, supporting its opposing role in neurosphere differentiation. Additional neurosphere differentiation experiments are underway to investigate possible additional roles of Patz1 in neuro-glial differentiation. Consistently, a recent study linked PATZ1 to neuron and glia differentiation through its interaction with the variant polycomb repressor complex 1 component PCGF1, which also interacts with NANOG and OCT4, and contribute to the maintenance of the undifferentiated phenotype of NT2 teratocarcinoma cell line that, upon treatment with all-trans retinoic acid, can differentiate to both neuron and glia (). Moreover, it has recently been shown that during neural differentiation, Nanog prevents the upregulation of genes important for neural specification (). As a further support, our previous studies have associated PATZ1 to cell plasticity, being it involved in both epithelial-mesenchymal and proneural-mesenchymal transition (; ).
It is well known that epigenetic mechanisms, including DNA and histone modifications, play critical roles in different stages of neurogenesis, and that aberrant epigenetic regulation also contributes to the pathogenesis of various brain disorders (). PATZ1 belongs to a large family of transcription factors, named POZ-ZF or POK, including BCL6, PLZF, TAZ1, and others, in which the POZ/BTB domain mediates protein-protein interactions, allowing the recruitment of histone deacetylases through co-repressor complexes (). PATZ1 is indeed an epigenetic regulator acting through the recruitment of repressor complexes that modulate histone deacetylase levels to the promoter of different genes (; ). Based on these findings, PATZ1 may be one of the key epigenetic factors that, by remodeling chromatin through the recruitment of histone deacetylases, is implicated in neurogenesis and, consequently, neurodegenerative and neuropsychiatric disorders. In this frame, the relatively high expression of PATZ1 in the hippocampus is particularly significant, where adult NSCs generate granular cells that confer the plasticity necessary for memory and behavior (; ). PATZ1 in these cells could be crucial for such plasticity, accounting for its involvement in depression (). Indeed, hippocampus is an important anatomical area associated with depression and studies have shown that some antidepressant can treat depression by changing the plasticity of the hippocampus (). Future experiments are needed to verify such hypothesis.
A tight link exists between NSCs and glioblastoma stem cells (GSCs). Glioblastoma (GBM) is the most frequent form of brain tumor in adults and is associated with a poor prognosis in both adults and children due to the poor tumor response to the limited available therapeutic options (). Various studies have suggested that NSCs might be the cells of origin of GBM, which arises from migration of mutated astrocyte-like NSCs (; ; ). We have previously shown that PATZ1 is overexpressed in both adult and pediatric GBM compared to normal glial cells (; ), and that it is specifically expressed in GSCs, where it is associated with the proneural phenotype (). Based on the results emerged from the present study, we could hypothesize that PATZ1 overexpression may contribute in maintaining the self-renewal and proliferative capacity of GSCs, likely favoring symmetric over asymmetric stem cell division. It is in fact known that both HMGA1 and p53, two PATZ1 interactors (; ; ), are deeply involved in the balance between symmetric and asymmetric stem cell division, which plays a key role in the expansion of the stem cell pool in both NSCs and GSCs (; ). Indeed, an undue increase in NSC symmetrical divisions, due to the disruption of molecular regulators, is the prelude to the conversion to GSCs and tumors in invertebrates (). Future molecular experiments are needed to clarify this possibility.
Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Ethics statement
The animal study was reviewed and approved by the Italian Ministry of Health (prot. no. 576/10 approved on 3 February, 2011). Written informed consent was obtained from the owners for the participation of their animals in this study.
Author contributions
MF: conceptualization, project administration, and original draft preparation. GLL and SM: methodology. SM, MV, and MD: validation. GLL and MF: formal analysis and supervision. SM, MV, MD, FM, GP, and AL: investigation. CA, GLL, and MF: resources. SM, GLL, and MF: data curation. SM, GLL, LC, and MF: writing, review and editing. LC and GLL: funding acquisition. All authors have read and agreed to the published version of the manuscript.
Funding
This study was supported by the funding from Associazione Italiana Ricerca sul Cancro (AIRC) to LC (IG 23052), from Regione Campania (PO FESR 2014−2020 SATIN) and from the European Union’s Horizon 2020 Research and Innovation Programme VES4US (Grant agreement no. 801338) to GLL.
Acknowledgments
We would like to acknowledge Antonio Simeone for the critical suggestions on in vivo BrdU-labeling, Sabrina Battista for the critical reading of the manuscript, Fabiana Franchini and Paola Francesca for the experimental contribution during their pre-graduate internships, the IGB Integrated Microscopy Facility for support in image acquisition, and the IGB Animal Facility for mice housing.
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.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcell.2021.657149/full#supplementary-material
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Summary
Keywords
neurogenesis, neural stem cells, PATZ1, knockout mice, neurosphere assay, subventricular zone
Citation
Mancinelli S, Vitiello M, Donnini M, Mantile F, Palma G, Luciano A, Arra C, Cerchia L, Liguori GL and Fedele M (2021) The Transcription Regulator Patz1 Is Essential for Neural Stem Cell Maintenance and Proliferation. Front. Cell Dev. Biol. 9:657149. doi: 10.3389/fcell.2021.657149
Received
22 January 2021
Accepted
15 March 2021
Published
07 April 2021
Volume
9 - 2021
Edited by
Carmen Castro, University of Cádiz, Spain
Reviewed by
Elena Parmigiani, University of Basel, Switzerland; Angela Fontan-Lozano, Seville University, Spain
Updates
Copyright
© 2021 Mancinelli, Vitiello, Donnini, Mantile, Palma, Luciano, Arra, Cerchia, Liguori and Fedele.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Monica Fedele, mfedele@unina.it; monica.fedele@cnr.it
†These authors share last authorship
‡Present address: Claudio Arra, Retired, Naples, Italy
This article was submitted to Stem Cell Research, a section of the journal Frontiers in Cell and Developmental Biology
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