Mitochondrial Transfer in Cardiovascular Disease: From Mechanisms to Therapeutic Implications
Jun Chen
Jinjie Zhong1 
Lin-lin Wang
Ying-ying Chen- 1Department of Basic Medicine Sciences, and Department of Obstetrics of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
- 2Department of Basic Medicine Sciences, and Department of Orthopaedics of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China
Mitochondrial dysfunction has been proven to play a critical role in the pathogenesis of cardiovascular diseases. The phenomenon of intercellular mitochondrial transfer has been discovered in the cardiovascular system. Studies have shown that cell-to-cell mitochondrial transfer plays an essential role in regulating cardiovascular system development and maintaining normal tissue homeostasis under physiological conditions. In pathological conditions, damaged cells transfer dysfunctional mitochondria toward recipient cells to ask for help and take up exogenous functional mitochondria to alleviate injury. In this review, we summarized the mechanism of mitochondrial transfer in the cardiovascular system and outlined the fate and functional role of donor mitochondria. We also discussed the advantage and challenges of mitochondrial transfer strategies, including cell-based mitochondrial transplantation, extracellular vesicle-based mitochondrial transplantation, and naked mitochondrial transplantation, for the treatment of cardiovascular disorders. We hope this review will provide perspectives on mitochondrial-targeted therapeutics in cardiovascular diseases.
Introduction
Cardiovascular diseases refer to a group of disorders affecting the heart and blood vessels, including coronary artery disease (such as myocardial infarction), arrhythmia, hypertensive heart disease, valvular heart disease, cardiomyopathy, et al. (1, 2). Mitochondria not only serve as power plants in cells but also act as crucial regulators in many biological processes, including reactive oxygen species (ROS) signaling, redox balance, calcium homeostasis, protein quality control, and programmed cell death (3, 4). The abnormal morphology and dysfunction of mitochondria have been proven as the principal mechanisms in the pathogenesis of cardiovascular diseases, such as heart failure, myocardial infarction, atherosclerosis, and hypertension (4–6). So mitochondria-targeted therapy is suggested to be a potential treatment strategy for cardiovascular diseases. In recent years, a large number of pharmaceutical compounds and nutritional supplements that can boost mitochondrial bioenergetics efficiency have been developed. However, clinical trials of these agents for cardiovascular diseases were hardly approved to carry out, even less to evaluate their clinical effectiveness and safety. The main obstacle is because many protein components of mitochondria are the network hubs of multiple biological pathways. If a chemical compound targeting one of these hubs is used, it can not only modify the anticipated biological pathways but also change other unexpected mitochondrial processes (5). Therefore, patients with cardiovascular diseases would fail to achieve the desired outcomes by using these mitochondrial-targeted drugs (5). Given the complexity of the biological function of mitochondria, researchers have begun to consider rescuing the injured cells through mitochondrial transfer, that is, replacing damaged mitochondria with healthy mitochondria from donor cells.
The intercellular mitochondrial transfer was reported for the first time by Spees and colleagues in 2006. They demonstrated that transferring functional mitochondria of bone marrow-derived stem cells to defective parenchymal cells increases the aerobic respiration capacity of recipient mitochondria (7). Nowadays, more and more studies have revealed that cells in the cardiovascular system (such as cardiomyocytes, vascular smooth muscle cells, endothelial cells, et al.) can act as donors or recipients during mitochondrial transfer under physiological conditions (8–12). However, harmful stimuli (such as ischemia-reperfusion, oxidative stress, and toxic chemicals) can change the direction and efficiency of intercellular mitochondrial transfer. Studies have shown that cells can eliminate defective mitochondria by delivering them to recipient cells (such as macrophages) to maintain homeostasis. And the released mitochondria can also act as a distress signal to activate the rescue properties of recipient cells (12, 13). Meanwhile, damaged cells can take up exogenous functional mitochondria and integrate them into endogenous mitochondria networks, which improve their biological process and enhance their repairability (14, 15). In this review, we summarized the mechanism and function of mitochondrial transfer in the cardiovascular system. We also discussed the advantages and challenges of mitochondrial transfer strategies in the treatment of cardiovascular disorders. We hope this review will provide perspectives on mitochondrial-targeted therapeutics in cardiovascular diseases.
Mechanisms of Intercellular Mitochondrial Transfer
Intercellular transfer of mitochondria in the cardiovascular system is through several pathways, including tunneling nanotubes (TNTs), extracellular vesicles (EVs), naked mitochondria extrusion, and others.
Mitochondrial Transfer via Tunneling Nanotubes
TNTs, also called membrane nanotubes, are long tubular membrane structures (Figure 1). TNTs were discovered as unique structures for intercellular communication for the first time by Rustom and coworkers in 2004 (16). Recent studies have shown that cells in cardiovascular systems (such as cardiomyocytes, cardiac fibroblasts, endothelial cells, and vascular smooth muscle cells) can exchange mitochondria with their neighboring cells via TNTs (Table 1) (8–12, 15, 17–24). The intercellular transfer of mitochondria through TNTs could be unidirectional or bidirectional. The diameter of TNTs ranges from 50 to 1,000 nm (8, 17, 21, 22, 24). The length of TNTs, which differs in various types of cells, is usually 5–120 μm (8, 9, 17). Actin is the principal component of TNTs, and filamentous actin (F-actin) polymerization is necessary for the assembly of TNTs (15, 18, 23). Besides actin, another cytoskeleton component, microtubule, is also found in some TNTs (23). Both F-actin and microtubules could act as cytoskeletal tracks for the movement of mitochondria. TNTs containing both microtubules and F-actin are large in diameter (>0.7 μm) and responsible for the long-distance delivery of mitochondria. TNTs containing only actin are small in diameter (<0.7 μm) and in charge of the short-distance transport of mitochondria (19, 21, 25–28).
Figure 1. Mitochondrial transfer via tunneling nanotubes (TNTs). TNTs are formed via cell dislodgment mechanism or actin-driven protrusion mechanism. TNTs containing only actin are small in diameter. TNTs containing both F-actin and microtubules are large in diameter. M-Sec is necessary for the formation of TNTs, while Cdc42 is required for the extension of TNTs. Mitochondrial Rho GTPase 1 (Miro1), a tail-anchored mitochondrial outer membrane protein, plays a critical role in mediating mitochondrial movement along the TNTs. After combing with the adaptor protein TRAK1/2, Miro1 can recruit motor protein kinesin and initiate microtubule-based mitochondrial movement. Miro1 can also mediate actin-based mitochondrial transport via binding with motor protein Myo19.
Table 1. Properties of mitochondrial transfer-related TNTs in cardiovascular system.
There are two different mechanisms involved in the formation of TNTs. (1) Cell dislodgment mechanism. Cells contact each other, then quickly migrate in opposite directions, retaining a thread of membrane between these two detached cells which finally develop into TNTs (9, 18). (2) Actin-driven protrusion mechanism. Filopodia-like membrane protrusions extend beyond the cell and elongate in an F-actin polymerization-dependent manner. Then the elongated protrusions connect with the target cells or other protrusions to form the TNTs (9, 12, 29). Unlike other cellular protrusions, these filopodia-like protrusions do not anchor to the substratum but suspend in the culture medium, which makes it possible for long-distance communication between cells (30).
M-Sec, also known as tumor necrosis factor α-inducible protein 2 (TNFαIP2), is reported as a key trigger of TNTs formation. Studies have shown that interaction of M-Sec with RalA can induce the assemble of exocyst complex and then initiate F-actin polymerization, while Cdc42 may be required for the extension process of TNTs (31). The expression of M-sec expression is regulated by many stimuli. Oxidative stress can activate p53, which in turn upregulates M-Sec expression by enhancing epidermal growth factor receptor expression or activating Akt/PI3K/mTOR pathway (32). Treatment of mesenchymal stem cells (MSCs) with TNF-α can increase M-Sec expression and trigger TNTs formation with cardiomyocytes via the NF-κB signaling pathway (15).
Some studies have demonstrated that gap junction protein connexin 43 (CX43) is necessary for TNTs formation and TNT-mediated intercellular mitochondrial transfer in non-cardiovascular systems (33–35). However, new evidence has shown that there is no Cx43 exists in the TNTs between cardiomyocytes and cardiac fibroblasts (9). Wang and coworkers have found that Cx43 only anchors at one end of TNT between two human umbilical vein endothelial cells (36). Since gap junctions do not allow the passage of large molecules (>1.2 kDa), Cx43 in the TNTs might only mediate intercellular electrical coupling but not cell-to-cell mitochondrial delivery (36). The role of Cx43 in the formation of TNTs and TNT-mediated mitochondrial transfer in the cardiovascular system still needs to be further explored.
Recently, mitochondrial Rho GTPase 1 (Miro1) has been reported to play a critical role in mediating mitochondrial movement along the TNTs (14, 15). Miro1 is a tail-anchored mitochondrial outer membrane protein. After combing with the adaptor protein TRAK1/2, Miro1 can recruit motor proteins (such as kinesin) and initiate microtubule-based mitochondrial movement (37). In a cardiomyocytes and cardiac myofibroblasts co-culture system, mitochondrial transport along microtubules in TNTs is mediated by KIF5B, which is a membrane of the kinesin superfamily (23). Recent studies have shown that Miro1 can also mediate actin-based mitochondrial transport via binding with motor protein Myo19 within individual mouse fibroblasts (38). However, whether Miro1 and Myo19 are involved in the mitochondrial movement along F-actin in TNTs still needs to be further investigated.
Mitochondrial Transfer via Extracellular Vesicles
Another pathway for cell-to-cell mitochondrial transfer is through EVs (Figure 2). The properties of EVs that transfer intact mitochondria or mitochondrial components in the cardiovascular system are listed in Table 2.
Figure 2. Mitochondrial transfer via EVs. The intercellular mitochondrial transfer can be mediated through EVs including exosomes, microvesicles, and exophers. Exosomes are smaller than microvesicles. Exophers are large membrane-surrounded microparticles usually containing damaged mitochondria and misfolded proteins. Exosomes or microvesicles can directly fuse with the recipient cell membrane or be engulfed by recipient cells through multiple pathways, including clathrin-dependent endocytosis, caveolin-mediated endocytosis, lipid raft-mediated endocytosis, phagocytosis, and micropinocytosis. Cardiac exophers can internalized into recipient cells via Mertk-mediated endocytosis.
Table 2. Characteristics of mitochondrial transfer-related EVs in cardiovascular system.
EVs are phospholipid membrane-bound microparticles released by cells. Exosomes and microvesicles are two major forms of EVs. Exosomes are small EVs (30–150 nm in diameter) that originated from the endosomal networks and are considered to deliver lipids, RNAs, and mitochondrial components (such as mtDNA). Microvesicles derived from cellular plasma membranes are larger than exosomes (100–1,000 nm in diameter) (43). Since mitochondria are elongated organelles with a diameter of 500–1,000 nm, the intact mitochondria more likely exist in the microvesicles but not in the exosomes (44). Many harmful stimuli, such as lipopolysaccharide, can induce endothelial cells to release EVs. Then the EVs are taken up by the recipient cells and cause inflammatory responses. The inflammatory responses might be due to the pro-inflammatory effect of mtDNA in the EVs (39, 41). On the contrary, hypoxia-injured cardiomyocytes can uptake the EVs containing respiratory-competent mitochondria to increase their rescue ability (40).
Recent studies have suggested that selective packaging of mitochondrial content into EVs depends on optic atrophy 1 (OPA1) and sorting nexin 9 (Snx9) proteins (45), but the exact mechanism is unclear. The formation of exosomes is initiated via membrane invagination to generate multivesicular late endosomes. Then the multivesicular late endosomes fuse with the plasma membrane, leading to the release of exosomes into the extracellular space. The biogenesis and release process of microvesicles is different from exosomes. Microvesicles are generated via membrane blebbing and then released into the extracellular environment by separating from the plasma membrane in Ca2+-dependent enzymatic machinery (46). Integrins on the surface of EVs have been widely reported as major regulators of anchoring EVs on recipient cells (47, 48). Once attaching the recipient cells, EVs can directly fuse with the recipient cell membrane or be engulfed by recipient cells through multiple pathways, including clathrin-dependent endocytosis, caveolin-mediated endocytosis, lipid raft-mediated endocytosis, phagocytosis, and micropinocytosis (49–51).
In 2020, a new type of mitochondria-containing EVs called exophers was discovered in hearts by Nicolas et al. (42). The structure of exophers from cardiac tissues is similar to that of neural exophers of C. elegans, which mainly contain misfolded proteins and damaged mitochondria (52). Different from the traditional EVs, cardiac exophers are large membrane-surrounded microparticles with an average diameter of 3.5 μm, which allows intact mitochondria to be packed in (42). The formation of cardiac exophers is motivated by the cardiac-specific autophagy mechanism. A large number of exophers extruded by cardiomyocytes can be engulfed by cardiac-resident macrophages via Mertk-mediated endocytosis. Such kind of crosstalk between cardiomyocytes and immune cells is required for the maintenance of mitochondrial fitness and cardiovascular health (42).
Mitochondrial Transfer via Naked Mitochondria Extrusion
Many studies have shown that the intact respiratory competent mitochondria exist in healthy human and animal blood which might be released by resting or activated platelets (53, 54). Likewise, mitochondria can also be released into the environment in the form of naked organelles by many normal or abnormal cells beyond platelets (54). For example, extracellular mitochondria are found in the endothelial progenitor cells culture system under physiological conditions (55). Monocytic cells can extrude naked mitochondria after being attacked by lipopolysaccharide (41). It has been proven that intact cell-free mitochondria are released from platelets through an actin-dependent but microtubule-independent mechanism (56).
However, the uptake mechanism of cell-free mitochondria by recipient cells has not been fully clarified. A few previous reports have shown that MSCs engulf platelet-derived functional mitochondria through clathrin-mediated endocytosis and enhance their pro-angiogenic activity (49). Some evidence has demonstrated that autologous mitochondria can be internalized into cardiomyocytes through actin-dependent endocytosis. Neither caveola-mediated nor clathrin-mediated endocytosis is involved in the mitochondrial internalization into cardiomyocytes (57). It has been reported that H9C2 rat cardiomyocytes can recognize and engulf exogenous mitochondria released from human uterine endometrial gland-derived MSCs in a co-incubation system. The uptake of mitochondria by cardiomyocytes is mainly via micropinocytosis (58). During the mitochondrial internalization process, cells can discriminate intact mitochondria from other similar microparticles and only engulf mitochondria (59). So the internalization mechanism of naked mitochondria might be different according to the types of recipient cells and the origin of naked mitochondria.
Mitochondrial Transfer via Other Pathways
Other pathways, such as cell fusion, are also found to be involved in intercellular mitochondrial transfer. In 2003, bone marrow-derived MSCs was reported to donate their mitochondria to cardiomyocytes through cell fusion. The cell fusion between MSCs and skeletal muscles is at a very low rate, suggesting that cell fusion is a kind of cell-specific machinery for cell-to-cell mitochondrial transfer (60).
Fate of Donor Mitochondria in Recipient Cells
Studies have shown that most healthy donor mitochondria can successfully escape from the endo-lysosomal system after being transferred into damaged cardiomyocytes and quickly integrate into the host mitochondrial network (61, 62). The combination of donor and recipient mitochondria within cardiomyocytes is a transient event that lasts about 4 h (62). The mechanism of mitochondrial integration might involve dynamic movements of mitochondrial fusion and fission. Many studies have demonstrated that mitofusin 1 (Mfn1) and Mfn2 are necessary for the fusion of mitochondrial outer membrane, optic atrophy 1 (Opa1) is responsible for the fusion of mitochondrial inner membrane (63), and dynamin-related protein 1 (Drp1) is required for mitochondrial fission (64, 65). In non-cardiomyocytes, mitochondrial transplantation can enhance the expression of Mfn2 and Opa1 and decrease the level of Drp1, which results in mitochondrial fusion (66). In the co-culture system of iPS-derived cardiomyocytes and cardiac fibroblasts, the mitochondrial fusion of donor and recipient mitochondria might be more likely due to the high Mfn1 and Opa1 protein levels in mitochondria (62). A minority of donor mitochondria that cannot flee from lysosomes undergo degradation through autophagy (62). This phenomenon has been confirmed by Louwagie and coworkers, whose studies have shown that the number of lysosomes in the recipient cells elevates after 4 h of mitochondrial transfer, accompanied by a higher mitophagy of donor mitochondria and a lower mitophagy of host mitochondria (61).
On the contrary, the main function of transferring defective mitochondria from damaged cells to healthy cells is to ask for help. After that, these foreign mitochondria in recipient cells will eventually be trapped in the LC3B-labeled phagosomes and eliminated via mitophagy, which ensures the normal functions of recipient mitochondria (14).
Besides mitochondrial fusion, a structure called mitochondrial nanotunnels also allows the exchange of matrix between two individual mitochondria. The mitochondrial nanotunnels in cardiomyocytes are a thin double-membrane tunneling structure with 40–200 nm in diameter and 0.7–14 μm in length (67, 68). Mitochondrial components like mitochondrial DNA, proteins, lipids can freely diffuse through the mitochondrial nanotunnels. Although the rate of mitochondrial matrix exchange via mitochondrial nanotunnels is slower than that of mitochondrial fusion mode, it provides the possibility for long-range communication between two individual mitochondria (67, 68). Whether the mitochondrial nanotunnels participate in the communication of donor and recipient mitochondria still needs to be further explored.
Role of Mitochondrial Transfer
Role of Mitochondrial Transfer Under Physiological Conditions
The cell-to-cell mitochondrial transfer has been detected in the cardiovascular system under physiological conditions (Table 3). In 2005, the unidirectional mitochondrial transfer from neonatal cardiomyocytes to endothelial progenitor cells was observed for the first time by Koyanagi et al. (8). After receiving donor mitochondria, endothelial progenitor cells acquire a cardiomyocyte-like phenotype through reprogramming (8). Meanwhile, a bidirectional mitochondrial transfer has been detected between cardiac myocytes and MSCs in a co-culture system (22). Migration of mitochondria from MSCs into fully differentiated cardiomyocytes can reprogram the adult cardiomyocytes and regress them to a progenitor-like state (20). Likewise, the mitochondrial transfer from embryonic cardiomyocytes to MSCs initiates stem cells differentiation toward cardiac cells, which might be an essential mechanism of stem cell-based therapies for cardiovascular disorders (22). Studies have also shown that mitochondrial transfer between vascular smooth muscle cells and MSCs is required to promote stem cells proliferation (10). These results suggest that intercellular mitochondrial transfer might play an important role in the regulation of cardiovascular system development.
Table 3. Role of mitochondrial transfer under physiological and pathophysiological conditions.
Although cardiomyocytes account for about 70–85% of the adult myocardial tissue volume (72), non-myocytes in cardiac tissues are essential for heart health. Cardiomyocytes and cardiac fibroblasts are the two most abundant cell types in mammalian hearts. Recent studies have demonstrated that mitochondrial exchange between cardiomyocytes and fibroblasts is a distinct intercellular communication pattern, which might be indispensable for normal cardiac function (9). But the exact molecular mechanism remains unclear. In 2020, Nicolas-Avila and colleagues found that cardiomyocytes can eliminate their abnormal mitochondria by delivering them to heart-resident macrophages under physiological conditions. Harmful stimuli, such as ischemia or isoproterenol challenge, can enhance the efficiency of mitochondrial transfer and accelerate the clearance of dysfunctional mitochondria (42). The mitochondrial transfer from cardiomyocytes to macrophages is beneficial to maintain the mitochondrial fitness of cardiomyocytes, reduce the accumulation of pro-inflammatory material, and prevent the activation of inflammasome (42). Studies have also demonstrated a low mitochondrial transfer between heart-resident macrophages and other non-myocytes (such as endothelial cells), suggesting intercellular mitochondrial transfer within the heart has a highly cell-specific feature. These studies demonstrated that cell-to-cell mitochondrial transfer might be essential for maintaining normal cardiac homeostasis.
Role of Mitochondrial Transfer Under Pathophysiological Conditions
Under pathophysiology conditions such as ischemic cardiomyopathy, damaged cells can not only release dysfunctional mitochondria to ask for help but also take up exogenous functional mitochondria to rescue their own mitochondria network (Table 3). The transfer of healthy mitochondria toward injured cells has multiple protective mechanisms include the following. (1) Improvement of mitochondrial biogenesis. The perturbation of mitochondrial biogenesis is known as the fundamental mechanism of cardiovascular diseases (6). Transfer of healthy mitochondria to the injured cardiomyocytes or endothelial cells can increase cellular ATP levels through elevating oxidative phosphorylation and tricarboxylic acid (TCA) cycle and reducing glycolysis (12, 15, 57, 61, 69). The improvement of mitochondrial biogenesis is due to the renewal of damaged mitochondrial DNA and increased expression of mitochondrial respiration-related protein through activation of peroxisome proliferator-activated receptor-gamma coactivator 1-alpha (PGC-1α)-mediated pathway (40, 57, 70, 71). It has been reported that this beneficial effect of the mitochondrial transfer can last for a long time (at least 28 days) in ischemic cardiomyocytes (73), which is in contrast to the short-term improvement of energy metabolism found in normal cardiomyocytes (74). (2) Enhancement of antioxidant capacity. Mitochondria are vital organelles that regulate redox balance via their pro-oxidant and antioxidant functions. Oxidative stress-induced injury is involved in the pathogenesis of many cardiovascular diseases, including atherosclerosis, myocardial ischemia-reperfusion injury, and hypertension (75–77). Inflammatory response, triggered by excessive ROS level, is also associated with vascular dysfunction in many pathophysiology conditions (78, 79). Recent studies have shown that the delivery of healthy mitochondria to cardiac cells or endothelial cells can protect them against oxidative damage (14, 70). Transplantation of MSCs to a doxorubicin-induced animal cardiomyopathy model also alleviates cardiac inflammation via mitochondrial transfer (15). The protective mechanism might be due to the overexpression of heme oxygenase-1, which has well-known properties of anti-oxidative and anti-inflammatory activities (14). (3) Reduction of apoptosis. Apoptosis is one of the most common patterns of programmed cell death in the cardiovascular system (80). Cardiomyocytes and endothelial cells are prone to apoptosis under various cellular stress (such as hypoxia, chemicals, and metabolic stress). Many studies have shown that transfer of healthy mitochondria to these injury cells can reduce apoptosis (11, 15, 18, 23, 69). The anti-apoptotic effect of mitochondrial transfer has been shown to have a gender-specific characteristic in pregestational diabetes mellitus-exposed offspring (61). The mechanism of mitochondrial transfer-induced anti-apoptosis might involve the decrease of Bax/Bcl-2 ratio and the inhibition of caspase-3 activity (11, 61).
In short, a series of studies implied the significance of mitochondrial transfer in the cardiovascular system. In physiological conditions, cardiac fibroblasts and cardiomyocytes show frequent intercellular communication through bidirectional mitochondrial transfer, which is critical in maintaining normal cardiac function (9). Although this phenomenon is observed in an in vitro model, whether it exists in vivo has not been confirmed. Meanwhile, transferring distressed mitochondria to macrophages is also critical to the fitness of cardiomyocytes (42). It is undoubted that mitochondria containing the information of donor cells once internalized into recipient cells can trigger a cascade of response, which in turn acts on donor cells. For instance, cardiomyocytes and endothelium suffered ischemia/reperfusion injury deliver mitochondria as signals to MSCs to ask for help. After receiving mitochondria, MSCs enhance the biogenesis of mitochondria and promote the capacity of anti-apoptosis, then generously donate functional mitochondria to distressed cells (14).
Therapeutic Strategies of Mitochondrial Transfer for Cardiovascular Diseases
Since transferring healthy mitochondria to damaged cells can alleviate injury and enhance the repairability of the target cells. Mitochondrial transplantation has been suggested as a promising therapeutic strategy for cardiovascular diseases. The most common methods of mitochondrial transplantation used for the treatment of cardiovascular diseases are cell-mediated therapy and cell-free therapy (including naked mitochondria transplantation and EV-based transplantation) (Figure 3 and Table 4).
Figure 3. Therapeutic strategies of mitochondrial transfer for cardiovascular diseases. The most common methods of mitochondrial transplantation used for the treatment of cardiovascular diseases (such as ischemic cardiomyopathy, anthracycline-induced cardiomyopathy) are cell-mediated therapy and cell-free therapy (including naked mitochondria transplantation and EV-based transplantation). Routes of administration can be intramyocardial injection, intracoronary delivery, and intravenous injection. After approaching the recipient cells, exogenous mitochondria can integrate with recipient mitochondria through mitochondrial fusion and fission machinery, or be trapped by lysosomes and be autophagy degraded. Some donor mitochondria might only communicate with recipient mitochondria via mitochondrial nanotunnels, without undergoing mitochondrial fusion. The transfer of healthy mitochondria toward injured cells has multiple protective mechanisms including improvement of mitochondrial biogenesis, enhancement of antioxidant capacity and reduction of apoptosis.
Table 4. Summary of mitochondrial transfer strategies for cardiovascular diseases.
Cell-Based Mitochondrial Transplantation
MSCs and progenitor cells have been recognized as the preferred mitochondria donors for the treatment of cardiovascular diseases due to their abundant sources and high mitochondrial respiratory activity. Animal experiments and clinical trials have shown that transplantation of MSCs can successfully repair injured myocardium in ischemic cardiomyopathy (81–84). The protective mechanism of MSCs therapy has been proven mainly via mitochondrial transfer in vitro or in vivo studies. For example, MSCs can prevent vascular endothelial cells injury in an ischemia-reperfusion model by enhancing aerobic respiration and reducing apoptosis through transferring mitochondria to endothelial cells (12). Mitochondria transferring from MSCs can protect cardiomyocytes against oxidative stress-induced injury by improving mitochondrial respiration function (11, 14, 15, 17, 70). MSCs transplantation has also been reported to reduce myocardial fibrosis, alleviate left ventricular dilatation, and improve cardiac function in an animal model of anthracycline-induced cardiomyopathy through mitochondrial transfer (15).
MSCs used in clinical trials can be originated from widely various tissues. Paliwal and coworkers have reported that the MSCs derived from pulp and Wharton's jelly have lower mitochondrial transfer abilities but higher mitochondrial respiration capacities than those of MSCs from bone marrow and adipose (70). Compared with bone marrow-derived MSCs, human-induced pluripotent stem cell-derived MSCs have higher efficiency of mitochondrial transfer due to their higher expression of Miro1 and TNFαIP2 (15). So the difference in mitochondrial transfer capacity and effectiveness of these tissue-specific MSCs need to be considered in cell-based therapy for cardiovascular diseases.
Whether the beneficial effect of MSCs transplantation is mainly due to mitochondrial transfer remains controversial. A few previous studies have reported that MSCs can rescue damaged cells through paracrine mechanisms (96). However, many in vitro studies have proven that the cardiovascular protective effect of stem cell-based therapy is mainly dependent on the transfer of functional mitochondria rather than the secretion of paracrine factors (12, 15). Since MSCs have limited trans-differentiation abilities into cardiomyocytes or other vascular components in vivo, it seems that the protective effect of MSCs transplantation is also unlikely due to their differentiation capacity (97). However, recent studies have shown that the emergence of many safety issues such as undesired differentiation, pro-arrhythmia, and microcirculation occlusion limit the clinical use of stem cell-based therapy (98–100).
Naked Mitochondria Transplantation
Naked mitochondrial transplantation refers to the transplantation of isolated and uncoated mitochondria to the injured tissues through circulation delivery or local injection (85, 86). The transplantation of naked mitochondria for the treatment of cardiovascular diseases can be traced back to 2009 when McCully's laboratory at Harvard demonstrated for the first time that intramyocardial injection of respiration-competent mitochondria could reduce infarct size and promote postischemic functional recovery in an animal model of heart ischemia-reperfusion injury (85). The optimal dose of mitochondria needed for efficiently protecting against ischemia-reperfusion injury ranges from 2 × 105 to 2 × 108 per gram wet weight (62, 71, 73, 87). Autologous mitochondria isolated from healthy cardiac or skeletal muscle are the dominant sources of donor mitochondria (85, 87, 101). The uptake of autologous mitochondria by cardiomyocytes is usually within minutes via internalization (62, 73). Exogenous mitochondria can also enter into cardiomyocytes without being cleared by lysosomes or autophagosomes. However, it takes more than 8 h for cardiomyocytes to engulf the xenogeneic mitochondria (73). In 2017, the first clinical use of mitochondrial transplantation was performed in five pediatric patients who suffered from cardiac ischemia-reperfusion injury. Four in five patients who accepted intramyocardial injection of autologous mitochondria have shown an improvement in ventricular function without any short-term side effects (such as arrhythmia, mitochondrial autoimmune response, and intramyocardial hematoma) (101).
Although intramyocardial injection of mitochondria has been proven efficient and safe in the treatment of myocardial ischemic disease, there are still a few limitations. For example, only a small number of donor mitochondria is allowed to inject within the myocardium per shot, and the percentage of mitochondrial internalization at each injection site is also pretty low (about 3–7%) (71, 73, 87). So multiple injections are required to ensure the extensive distribution of donor mitochondria throughout the ischemic heart, which increases the difficulty of operation. In addition, the need for thoracotomy prior to the intramyocardial injection may also be a huge obstacle limiting the clinical application of mitochondrial transplantation for potential patients (101).
Since 2016, researchers have begun to test the feasibility of intracoronary delivery as an alternative mitochondrial transplantation method (88). Both autologous and exogenous mitochondria can rapidly spread throughout the whole heart within 10 min of coronary perfusion rather than occur in clusters as found in intramyocardial injection. Furthermore, intracoronary delivery also results in a higher mitochondrial internalization into cardiomyocytes (~23%) than intramyocardial injection (88). In animal models of regional ischemia-reperfusion injury, both preischemic or postischemic intracoronary injection of autologous mitochondria can decrease infarct size, enhance coronary blood flow, and increase cardiac function (88–91). Intracoronary injection of healthy mitochondria also has powerful cardiac protection against globally ischemic injury of donor hearts and global ischemia/reperfusion injury of diabetic heart (88, 92–94). No signs of microvascular obstruction and cardiac arrhythmia are observed after intracoronary injection of mitochondria (91). The safety and efficacy of intracoronary delivery of mitochondria make it a promising treatment for myocardial infarction through percutaneous coronary intervention.
Considering the clinical use of mitochondrial transplantation, intravenous injection of mitochondria might be more feasible than intramyocardial and intracoronary administration. Intravenous delivery of mitochondria has been used as a promising therapeutic method for fatty liver and Parkinson's disease (102, 103). Recent studies have shown that intravenous injection of viable exogenous mitochondria for 3 weeks can improve right ventricular function in an animal model of pulmonary hypertension (86). After systemic administration, the mitochondria are observed in various tissues, including heart (102, 103). The stability of naked mitochondria in the bloodstream and tissue-specific delivery may be the key factors for successful therapy in ischemic or non-ischemic cardiovascular disorders.
Besides ischemic heart injury, recent studies have also found that mitochondrial transplantation can delay the progression of right heart failure (86, 95) and improve myocardium metabolism of offspring born to diabetic mothers (61). Although studies have confirmed the efficiency of naked mitochondrial transplantation, how to obtain high yields of good-quality mitochondria is still a challenge. Enhancing the efficiency of mitochondrial internalization into target cells and maintaining the viability of transferred mitochondria are also crucial problems to assure the efficient clinical application of naked mitochondria transplantation.
EV-Based Mitochondrial Transplantation
Another method of cell-free therapy is mitochondria-rich EVs transplantation. EVs have been recognized as a powerful platform for mitochondrial delivery (40, 104, 105). MSCs from different tissues are the main sources of EVs (106). Although many studies have proven that MSCs-derived EVs can serve as a potential therapy for the treatment of cardiovascular disease, whether the protective effect is mainly dependent on their mitochondria cargo is unclear (107). In 2021, Ikeda's laboratory at Stanford isolated some mitochondria-rich EVs from human-induced pluripotent stem cell-derived cardiomyocytes. The diameter of these EVs ranges from 98 to 677 nm (40). The outer lipid bilayer of EVs usually serves as a security guard that keeps the mitochondria maintaining their morphological and functional integrity. The mitochondria encapsulated within EVs are found more stable than naked mitochondria under extracellular environmental stress, such as calcium overload and oxidative stress (40). In vitro and in vivo studies have demonstrated that transplantation of mitochondria-rich EVs can restore intracellular bioenergetics, prevent post-ischemic left ventricular remodeling, and improve myocardial contractility (40). Since the diameters of MSC-derived EVs are usually <10 μm (108), intravenous or intracoronary injection of EVs has no risk of microvascular obstruction. The intramyocardial injection of mitochondria-rich EVs into the peri-infarct region does not induce cardiac arrhythmia (40), which supports the opinion of Adamiak and coworkers that MSC-derived EVs are safer than MSCs (109). The cargo content of EVs mainly includes mitochondria and their components, nucleic acids, lipids, and proteins, which can be altered according to their cellular origins and isolation methods (107). The complex composition of different EVs makes them have distinctive mechanisms and effects on various diseases. Ikeda and coworkers have found that the beneficial effect of mitochondria-rich EVs transplantation on myocardial ischemia-reperfusion injury was not only due to mitochondria cargo but also due to non-mitochondrial cargo (40). In order to reduce the heterogeneity of EVs and guarantee the therapeutic effect, it is necessary to set up a standardized EV isolation protocol. Meanwhile, how to improve the targeting specificity of EVs is also an issue needed to be further investigated (110).
In conclusion, many in vivo studies have proven the effectiveness of mitochondrial transplantation in the treatment of different cardiovascular diseases. Ischemia/reperfusion injury is one of the most common diseases in the cardiovascular system. Researchers delivered mitochondria to rescue damaged cardiac tissue through different administrational routes in various species (14, 40, 69, 73). Comfortingly, all of these studies have confirmed the significant improvement of cardiac function after mitochondrial transplantation. In a clinical trial, autologous mitochondria from skeletal muscle were injected into the damaged cardiomyocytes of pediatric patients suffering ischemia/reperfusion injury, which effectively promote the recovery of postischemic myocardium without adverse short-term complications (101). Functional mitochondrial delivery has been used for some other cardiovascular diseases (including heart failure, anthracycline-induced cardiomyopathy, pregestational diabetes-induced cardiac malfunction, heart transplantation) and to some extent improve the prognosis (15, 61, 70, 94).
Ethical Issues
In 2015, the United Kingdom became the first country in the world to legislate and permit the clinical use of mitochondrial donation technology (111). However, there are still controversies about the ethical issues of the mitochondrial transfer strategy. (1) Mitochondrial-nuclear incompatibility. Studies have shown that the efficiency of cellular energy metabolism depends on about 2000 mitochondrial proteins. Most of these proteins are encoded by the nuclear genome, and only 13 proteins are encoded by the mitochondrial genome (112). So the compatibility of donor mitochondria and recipient cell nuclei is critical for the normal mitochondrial respiratory function of recipient cells (113–115). Many researchers have suggested that mitochondria originated only from the same cells or species are the ideal donors for reducing mitochondria-nuclear incompatibility and ensuring successful mitochondrial transfer (116, 117). (2) Transmission of detrimental mutation. The mutation rate of mtDNA is significantly higher than that of nuclear DNA due to a lack of histone protection and less efficient repairability (118). Meanwhile, studies have shown that mitochondrial fragmentation of donor mitochondria increases when using the standard mitochondrial isolation methods. And elevated mitochondrial fission is closely related to mtDNA abnormalities (119, 120). The mutated mtDNA of donor mitochondria can be transmitted to the recipient cells during intercellular mitochondrial transfer. When the accumulation of mutated mtDNA exceeds the threshold, cellular dysfunction, and abnormal morphology will occur (121). Such detrimental effects on recipient cells might be unpredictable due to intra- and inter-cellular mitochondrial heterogeneity (122). Therefore, the establishment of ethical guidelines is a prerequisite for ensuring the safe application of mitochondrial transfer strategies in the treatment of cardiovascular diseases.
Discussion and Future Perspectives
Mitochondrial dysfunction plays a crucial role in the development and progression of cardiovascular disorders, which provides the possibility for mitochondrial transfer as an effective therapeutic strategy in the treatment of cardiovascular diseases. With the emergence of new technologies, trends in mitochondrial transplantation therapeutics are changing from cell-based to cell-free therapy. EVs-based mitochondrial delivery is considered more promising than naked mitochondria transplantation in the treatment of cardiovascular diseases, but it still has some limitations. Recently, some researchers developed a new delivery system by artificially encapsulating isolated mitochondria with some biocompatible polymers (such as dextran triphenylphosphonium complexes, transactivator of transcription dextran complexes) (69, 123). The polymer-coated delivery system, which almost exclusively contains mitochondria, is considered better than the EV-based delivery system. Meanwhile, the polymer-coated mitochondria have a higher transfer efficiency and a more powerful rescue capability than those of naked mitochondria, suggesting that they might become a more feasible and promising strategic alternative for mitochondrial transplantation in the future (69, 123). Although many preclinical experiments have proven the advantages of mitochondrial delivery in treating cardiovascular diseases, there are still a few technical challenges and ethical issues that need to be resolved (124). The efficiency and safety of mitochondrial transplantation in treating cardiovascular diseases still need to be further evaluated before conducting clinical trials.
Author Contributions
JC wrote the manuscript and prepared the tables. JZ wrote the manuscript and made the figures. L-lW and Y-yC edited the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the National Natural Science Foundation of China (Grant Numbers: 81871541 and 81471837).
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
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Keywords: cardiovascular disease, mitochondria, mitochondrial transfer, mitochondrial transplantation, tunneling nanotubes, extracellular vesicles
Citation: Chen J, Zhong J, Wang L-l and Chen Y-y (2021) Mitochondrial Transfer in Cardiovascular Disease: From Mechanisms to Therapeutic Implications. Front. Cardiovasc. Med. 8:771298. doi: 10.3389/fcvm.2021.771298
Received: 06 September 2021; Accepted: 08 November 2021;
Published: 26 November 2021.
Edited by:
Xiaofeng Yang, Temple University, United StatesReviewed by:
Sandra Anjo, University of Coimbra, PortugalRuijing Zhang, Second Hospital of Shanxi Medical University, China
Copyright © 2021 Chen, Zhong, Wang and Chen. 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: Lin-lin Wang, wanglinlin@zju.edu.cn; Ying-ying Chen, bchenyy@zju.edu.cn