- Open Access
microRNA-378 promotes mesenchymal stem cell survival and vascularization under hypoxic–ischemic conditions in vitro
Stem Cell Research & Therapy volume 5, Article number: 130 (2014)
Mesenchymal stem cells (MSCs) transplantation has been demonstrated to be an effective strategy for the treatment of cardiovascular disease. However, the low survival rate of MSCs at local diseased tissue reduces the therapeutic efficacy. We therefore investigated the influence of MicroRNA-378 (miR-378) transfection on MSCs survival and vascularization under hypoxic-ischemic condition in vitro.
MSCs were isolated from bone marrow of Sprague–Dawley rats and cultured in vitro. The third passage of MSCs were divided into the miR-378 group and control group. For the miR-378 group, cells were transfected with miR-378 mimic. Both groups experienced exposure to hypoxia (1% O2) and serum deprivation for 24 hours, using normoxia (20% O2) as a negative control during the process. After 24 hours of reoxygenation (20% O2), cell proliferation and apoptosis were evaluated. Expressions of apoptosis and angiogenesis related genes were detected. Both groups were further co-cultured with human umbilical vein endothelial cells to promote vascular differentiation for another 6 hours. Vascular density was assessed thereafter.
Compared with the control group, MSCs transfected with miR-378 showed more rapid growth. Their proliferation rates were much higher at 72 h and 96 h under hypoxic condition (257.33% versus 246.67%, P <0.01; 406.84% versus 365.39%, P <0.05). Cell apoptosis percentage in the miR-378 group was significantly declined under normoxic and hypoxic condition (0.30 ± 0.10% versus 0.50 ± 0.10%, P <0.05; 0.60 ± 0.40% versus 1.70 ± 0.20%, P <0.01). The miR-378 group formed a larger number of vascular branches on matrigel. BCL2 level was decreased accompanied with an upregulated expression of BAX in the two experimental groups under the hypoxic environment. BAX expression was reduced in the miR-378 group under the hypoxic environment. In the miR-378 group, there was a decreased expression of tumor necrosis factor-α on protein level and a reduction of TUSC-2 under normoxic environment. Their expressions were both downregulated under hypoxic environment. For the angiogenesis related genes, enhanced expressions of vascular endothelial growth factorα, platelet derived growth factor-β and transforming growth factor-β1 could be detected both in normoxic and hypoxic-ischemic conditions.
MiR-378 transfection could effectively promote MSCs survival and vascularization under hypoxic-ischemic condition in vitro.
Cardiovascular disease with resultant heart failure and malignant arrhythmia is a major cause of morbidity and mortality worldwide . In recent years, stem cell therapy has emerged as a novel strategy for the treatment of cardiovascular disease, and its beneficial efficacies have been confirmed by various preclinical and clinical trials [2–5]. Bone marrow mesenchymal stem cells (MSCs), which have great potential for proliferation and differentiation, have the capacity to differentiate into cardiomyocytes and vascular cells under appropriate conditions [6, 7]. Implantation of MSCs results in regeneration of cardiomyocytes and neovascularization in myocardial infarction. Moreover, these cells can confer protection to ischemic tissues through the release of paracrine factors, thus providing a promising therapeutic modality for repair of the injured heart [8–10]. A series of clinical trials have already shown that MSCs treatment can attenuate ventricular remodeling and improve cardiac function in patients with myocardial infarction and chronic heart failure [4, 5, 11, 12]. However, inferior survival of MSCs under hypoxic condition reduces their therapeutic efficacy [13, 14]. Low survival rates of the donor cells could be due to inflammation, ischemia and apoptosis [15, 16]. Therefore, how to enhance MSCs survival and promote their vascularization in the local hypoxic environment becomes a main issue that needs to be addressed in order to improve the clinical benefits of MSCs transplantation.
microRNAs (miRNAs) are small noncoding RNAs that control gene expression post-transcriptionally. They exert functions over a wide range of cellular processes, including the regulation of stem cell pluripotency and differentiation . Manipulation of miRNAs in stem cells may enhance their capacity for cell survival and vascular regeneration [18, 19]. miRNAs can promote MSCs differentiation into cardiovascular cell lineage and affect MSCs-mediated cardiac repair . microRNA-378 (miR-378) is a specific miRNA that can induce angiogenesis in tumors . Experimental studies show that miR-378 transfection significantly enhances cell viability and inhibits cell apoptosis [22, 23]. In addition, miR-378 is a newly described member of the cardiac-enriched miRNAs modulating cardiac growth during the postnatal period . Its deficiency leads to the development of cardiac hypertrophy . A distinct reduction of miR-378 in patients with heart failure has been reported, implying that it may also participate in the disease progression of heart failure .
miR-378 is closely associated with stem cell survival and vascular differentiation. In this study, MSCs were transfected with miR-378 and exposed to normal and hypoxic–ischemic conditions to observe their survival, proliferation and apoptosis. Vascular density was evaluated and the expression of molecules related to apoptosis and vasculogenesis was detected.
Materials and methods
One-month-old Sprague–Dawley rats were obtained from the Animal Experimental Center of the Sun Yat-sen University (Guangzhou, China). All animal handling and procedures were performed in accordance with protocols approved by the Animal Ethics Committee of Sun Yat-sen University (201210016).
Isolation and culture of bone marrow mesenchymal stem cells
Bone marrow cells were collected from 1-month-old Sprague–Dawley rats by flushing femurs and tibias under sterile conditions. The cells were then cultured (37°C, 5% carbon dioxide) in 25 cm2 culture flasks with complete culture medium supplemented with 10% fetal bovine serum penicillin (100 IU/ml) and streptomycin (100 μg/ml). On the third day of culture, the medium was replaced and nonadherent cells were removed. Adherent cells gaining 90% confluence were passaged using 0.25% trypsin–ethylenediamine tetraacetic acid (Mediatech, Hendon, VA, USA) and then maintained in complete medium. Characteristics of MSCs were identified by fluorescence-activated cell sorting as reported previously .
miR-378 mimic (mature sequence rno-miR-378a-5p: 4-cuccugacuccagguccugugu-25) was synthesized and provided by Ruibo Biotechnology Corporation (Guangzhou, China). To obtain MSCs overexpressing miR-378 effectively, third-passage MSCs were transfected with miR-378 mimic using Lipofectamine™ 2000 (catalogue number 11668019; Invitrogen, Carlsbad, California, USA) according to the manufacturer’s instructions. Opti-MEM (catalogue number 31985070; Invitrogen) was applied as transfection medium and the medium was changed 4 hours after transfection. Total RNA and cell lysate were collected for the indicated assays.
Hypoxia/reoxygenation treatments of MSCs
Twenty-four hours after transfection, cells of the miR-378 group (MSCs transfected with miR-378) and the control group (MSCs without transfection) were both incubated in serum-free media with 1% oxygen in a Galaxy® 48 R incubator (Eppendorf/Galaxy Corporation, Connecticut, USA) at 37°C for 24 hours and then exposed to normoxic conditions (20% oxygen) for another 24 hours. Normoxia was used as negative control during the experiments for the two groups.
Survival and apoptosis evaluation of MSCs
After the above treatments, the MSCs of different groups were collected and suspended in complete culture medium. The growth curve and MTS assay (cellTiter96AQ, one solution cell proliferation assay, catalogue number G3582; Promega, Madison, Wisconsin, USA) were adopted to evaluate survival and proliferation ability of MSCs. A total of 1 × 105 cells were equally seeded into each well on 96-well plates. After 24 hours of preconditioning, MTS was added to the medium at a final concentration of 0.5 mg/ml for 4 hours. Results were read from cellTiter96AQ at different time points (24, 48, 72 and 96 hours) respectively.
The terminal deoxynucleotidyl transferase biotin-dUPT nick end-labeling assay was applied for assessing MSC death and apoptosis in vitro after 24 hours of reoxygenation. Cell slices were fixed in 10% formaldehyde for 15 minutes and pretreated with 0.2% Triton X-100 for 15 minutes. The slices were then infiltrated in an equilibration buffer followed by incubating with terminal deoxynucleotidyl transferase enzyme and a nucleotide mix for another 75 minutes. All sections were examined under a florescent microscope (DMI6000B; Leica, Brunswick, Germany).
Vascular networks formation assay of MSCs
Aliquots of human umbilical vein endothelial cells (Yiyuan Biotechnology Corporation, Guangzhou, China) were seeded onto matrigel-coated wells (catalogue number 356234; BD Corporation, New York, USA) of a 24-well plate. After hypoxia/reoxygenation treatments, MSCs were then cocultured with human umbilical vein endothelial cells in 1% fetal calf serum-supplemented Dulbecco’s modified Eagle’s medium (catalogue number SH30021.01B; Hyclone, Logan City, Utah, USA). After incubating at 37°C for 6 hours, vascular network formation was examined by a phase-contrast microscopy (CKX41, U-CTR30-2; Olympus, Tokyo, Japan), and the number of the vascular branches was quantified by randomly selecting five fields per well as described previously .
Western blot analysis
Protein levels of BCL2, BAX, tumor necrosis factor alpha (TNFα), TUSC-2, vascular endothelial growth factor (VEGF) alpha, platelet-derived growth factor (PDGF) beta and transforming growth factor beta-1 (TGFβ1) were measured by western blot. After 24 hours of reoxygenation, MSCs were washed several times with phosphate-buffered saline before collection and lysing with modified RIPA buffer. Cells were completely lysed after repeated vortexing and supernatants were acquired though centrifugation at 14,000 × g for 20 minutes. Proteins were then resolved by SDS-PAGE and subsequently transferred to a polyvinylidenedifluoride membrane (IPVH00010; Millipore, Boston, MA, USA) before incubating with primary antibodies overnight at 4°C. The membranes were subjected to three 5-minute washes with Tris-buffered saline–Tween and then incubated with anti-IgG horseradish peroxidase-conjugated secondary antibody (Southern Biotech, Birmingham, Alabama, USA) for 60 minutes at room temperature. After extensive washing, bands were detected by enhanced chemiluminescence. The band intensities were quantified using image software (image J 2×, version 18.104.22.168).
Quantitative real-time polymerase chain reaction
Total RNA was isolated from MSCs with hypoxia/reoxygenation treatments using a Trizol reagent (Invitrogen) followed by digestion with RNase-free DNase (Promega). The concentration and integrity of total RNA were estimated and the real-time polymerase chain reaction (RT-PCR) was conducted on an ABI PRISM® 7500 Sequence Detection System using SYBR Green qPCR SuperMix (Invitrogen). The primers are described in Table 1. Specific products were amplified and detected at 95°C for 10 minutes, followed by 40 cycles at 95°C for 15 seconds, and at 60°C for 30 seconds, at which point data were acquired. The miR-378 expression level was quantified using probes for miR-378 and U6 RNA (internal control). The relative level of miRNA was calculated using the 2-ΔΔCt method. For the assays of the molecules examined, the results were quantified as the threshold cycle of each target gene and normalized into the ΔCt value. Quantifications of fold-change in gene expressions were also performed using the 2-ΔΔCt method.
All quantitative data are described as mean ± standard deviation. The significance of differences among groups was determined by analysis of variance and Scheffe’s multiple-comparison techniques. Comparisons between time-based measurements within each group were performed with analysis of variance for repeated measurements. P <0.05 was considered statistically significant.
Mesenchymal stem cells survival was enhanced post transfection of miR-378
miR-378 expression status after transfection with miR-378 mimic was confirmed by quantitative RT-PCR (P < 0.01; Figure 1A) The two experimental groups presented a lower growth and proliferation rate under a hypoxic environment at 72 hours and 96 hours, while both groups showed a higher inhibition rate in this condition (P < 0.01; Figure 1B, C, D). The miR-378 group displayed a more rapid growth under hypoxic environment at 72 hours and 96 hours in contrast with the control group (0.78 ± 0.02 vs. 0.73 ± 0.02, P < 0.05; 1.22 ± 0.03 vs. 1.08 ± 0.03, P < 0.05) (Figure 1B). Moreover, the transfected cells had a higher proliferation rate (257.33% vs. 246.67%, P < 0.01; 406.84% vs. 365.39%, P < 0.05) (Figure 1C). The inhibition rate of the miR-378 group was lower under a hypoxic environment at 72 hours and 96 hours (3.73% vs. 9.47%, P < 0.01; 1.63% vs. 13.60%, P < 0.01) (Figure 1D), indicating that miR-378 could alleviate the inhibition of MSC proliferation induced by hypoxia–ischemia.
Hypoxia-induced apoptosis in MSCs was alleviated after miR-378 transfection
The two groups both exhibited a higher apoptosis rate under the hypoxic environment (0.50 ± 0.10% vs. 1.7 ± 0.20%, P < 0.01; 0.30 ± 0.10% vs. 0.60 ± 0.40%, P < 0.01) (Figure 2B). Compared with the control group, terminal deoxynucleotidyl transferase biotin-dUPT nick end-labeling staining showed that the apoptosis rate of the miR-378 group was significantly decreased under normal (0.30 ± 0.10% vs. 0.50 ± 0.10%, P < 0.05; Figure 2A, B) and hypoxic (0.60 ± 0.40% vs. 1.70 ± 0.20%, P < 0.01; Figure 2A, B) environments.
Angiogenesis ability of MSCs was promoted after miR-378 transfection
Once cocultured with human umbilical vein endothelial cells, MSCs transfected with miR-378 formed a larger number of vascular branches on matrigel. Under normoxic conditions, the numbers of vascular branches in the miR-378 group were obviously higher than in the control group (17.50 ± 0.55 vs. 15.17 ± 1.17, P < 0.01). The same phenomenon could be observed when the two groups of cells were exposed to a hypoxic–ischemic environment (18.00 ± 1.79 vs. 14.67 ± 1.03, P < 0.01) (Figure 3).
Expression of apoptosis-related genes was decreased after miR-378 transfection
The expression of apoptosis-related genes was examined by western blot and quantitative RT-PCR in both groups after cells experienced hypoxia/reoxygenation or were exposed to normoxic (20% oxygen) conditions (Figure 4). Detection of the BCL2 family proteins showed that the BCL2 level was decreased, accompanied with an elevated expression of BAX in the two experimental groups under a hypoxic environment (Figure 4A, C, D). There was no difference of the expression of BCL2 between the miR-378 group and the control group under normoxic and hypoxic environments (Figure 4A, C), whereas BAX expression was reduced in the miR-378 group under a hypoxic environment (Figure 4A, D). The TNFα level was increased under the hypoxic environment in the two groups (Figure 4B, E). In the miR-378 group, TNFα protein expression was decreased under the normoxic environment (Figure 4B) and its expression was downregulated both on mRNA and protein level in hypoxic conditions (Figure 4B, E). TUSC-2 expression was enhanced on the protein level under a hypoxic environment in the two groups (Figure 4B). Its level was downregulated in the miR-378 group compared with the control group under normoxic and hypoxic environments (Figure 4B, F).
Expression of angiogenesis-related genes was enhanced after miR-378 transfection
Angiogenesis-related genes were detected the same way as described above. The expression of VEGFα, PDGFβ and TGFβ1 was decreased in the control group under hypoxic conditions (Figure 5). However, no differences in their expressions were observed in the miR-378 group when exposed to the same environment (Figure 5). Western blot analysis showed that the expression of VEGFα, PDGFβ and TGFβ1 was increased in miR-378 transfected MSCs under both normoxic and hypoxic conditions (Figure 5A). Quantitative RT-PCR indicated that there was an upregulated expression of PDGFβ on the mRNA level (Figure 5C), whereas no differences could be discovered in the expressions of VEGFα and TGFβ1 genetically (Figure 5B, D).
The present study demonstrates that MSCs transfected with miR-378 showed higher viability and a lower apoptosis rate under hypoxic–ischemic conditions. Moreover, their capacity for blood vessel formation was improved. The expression of proapoptosis genes was decreased whereas angiogenesis-related genes were found to be upregulated after miR-378 transfection.
MSCs are multipotent progenitor cells with the potential to differentiate into various cell types, including cells of the cardiovascular lineage . MSCs can be easily isolated and expanded in vitro, making them an optimal therapeutic approach for cardiovascular disease . In spite of this, the low survival rate of MSCs after transplantation in vivo restricts their therapeutic efficiencies [13, 14]. Studies have indicated that hypoxia and serum deprivation can lead to poor viability and apoptosis of MSCs via triggering a strong inflammatory and oxidative stress reaction and an overproduction of proapoptosis factors [15, 30]. Diverse methods have been applied to improve MSCs survival under hypoxic and ischemic conditions [16, 31]. miRNAs play a crucial role in cell proliferation, differentiation and apoptosis . It has been reported that transfection of specific miRNAs enhances MSCs survival and their capability for lineage differentiation, making them more conducive to the repair of infarct injury . Prior studies have demonstrated that miR-378 facilitates cancer cell migration and promotes their survival . In this study, we investigated the effects of miR-378 on MSCs survival and proliferation. The results indicated that MSCs could be efficiently transfected with miR-378 without affecting cells viability. We found that MSCs viability was attenuated under the hypoxic condition in the two experimental groups. Cells transfected with miR-378 showed more rapid growth and a higher proliferation rate after 24 hours of hypoxia/reoxygenation. Examination of the apoptosis of MSCs showed that the number of terminal deoxynucleotidyl transferase biotin-dUPT nick end-labeling-positive cells was significantly decreased in the miR-378 group. In addition, MSCs transfected with miR-378 presented a distinctly lower apoptosis rate compared with the control group, suggesting that miR-378 might exert anti-apoptosis roles in a hypoxic–ischemic environment in vitro.
Evidence has revealed that miR-378 improves cell survival and inhibits apoptosis via regulation of various signaling networks and apoptosis-related genes . miR-378 may reduce hydrogen peroxide and hypoxia-induced cell death by suppressing the expression of IGF-1R and its downstream AKT signaling cascade . The proteins of the BCL2 family are well known as key regulators of cell death and apoptosis. Increasing evidence sustains that BCL2 family members are the targets of numerous miRNAs . In the present work, we examined several BCL2 family proteins including BCL2 and BAX. We found that BCL2 was downregulated while BAX was upregulated in the two experimental groups under the condition of hypoxia exposure. In the miR-378 group, there was no alteration of the expression of BCL2 both under the normoxic and hypoxic conditions, while the BAX level was decreased in the hypoxic condition, implying that miR-378 could attenuate the apoptosis of MSCs via suppressing the proapoptosis genes of the BCL2 family. In addition to the BCL2 family, TUSC-2 (also known as Fus-1) is a potent proapoptotic gene . The expression of the miR-378/miR-378 hairpin enhances cell survival through targeting the transcription factor SuFu and Fus-1 . Moreover, miR-378 is capable of reducing the expression of TUSC-2 at the protein level . TNFα is another pivotal molecule that initiates the process of MSC apoptosis . TNFα represses the expression of proinflammatory genes by activating nuclear factor-κB . TNFα can also stimulate the caspase cascade related to cell apoptosis . In this study, the expression of TUSC-2 protein was upregulated and the TNFα level was enhanced in the two groups under hypoxic environments. Both the expressions of TUSC-2 and TNFα were downregulated in miR-378-transfected MSCs under a hypoxic environment, implicating that miR-378 may relieve hypoxia-induced apoptosis via downregulating TUSC-2 and TNFα.
miRNAs can exist in a lineage-specific pattern and dominate the fate of stem cell differentiation . Several miRNAs have already been found to modulate cardiovascular cell differentiation [20, 39]. Previous studies have confirmed that miR-378 plays an important role in blood vessel formation [40, 41]. In the present study, we demonstrated that MSCs transfected with miR-378 formed a larger number of vascular branches on matrigel, indicating that miR-378 could enhance the capability of MSCs differentiation into vascular lineage.
miRNAs most probably control cell fate via regulating numerous genes and pathways [17, 20]. VEGF has been identified as a predominant mediator of angiogenesis . VEGF hampers post-hypoxic MSC death and improves MSCs survival and regeneration in hostile environment of post-ischemic tissues [43, 44]. miR-378 is involved in the expression of VEGF . miR-378 binds to the 3′ untranslated region of VEGF to compete with miR-125a for the same seed region and strengthens VEGF expression . In this study, VEGFα expression was found to be declined in the control group after hypoxia exposure and this alteration could be mitigated after miR-378 transfection. In addition, VEGFα expression was increased at the protein level in the miR-378 group in hypoxic conditions. The abovementioned results supported that MSCs might strengthen VEGF expression in the context of hypoxia exposure. PDGF and TGFβ1 secreted by MSCs profoundly impact vascularization as well as proliferation of MSCs [20, 46]. We found that the expression of PDGFβ and TGFβ1 was also downregulated under hypoxic conditions in the control group; PDGF receptors can effectively induce MSCs neovascularization in vivo. When the expression of PDGF is depressed, pathways associated with angiogenesis of MSCs are correspondingly obstructed . miRNAs modulate PDGF receptor expression upon ligand stimulation through direct interaction with the 3′ untranslated region of PDGF receptor in cardiomyocytes . In the present work, PDGFβ was increased in MSCs transfected with miR-378 under normoxic and hypoxic conditions, indicating that miR-378 might improve PDGF expression in this condition. MSCs have the potential to differentiate into smooth muscle cells, which makes them an ideal cell source for the construction of tissue-engineered vascular grafts . TGFβ1 is a cytokine with versatile functions . This cytokine can induce smooth muscle markers in MSCs, subsequently driving MSCs toward a smooth muscle cell phenotype . TGFβ1 signaling has important functions in the regulation of MSCs at both transcriptional and post-transcriptional levels . High concentrations of TGFβ1 contribute to the formation of nestin-positive MSC clusters, resulting in shaping of marrow osteoid islets accompanied by high levels of angiogenesis . miRNAs have been proved to mediate TGFβ-induced signaling circuit loops in the pathological process of human diseases . They regulate TGFβ1 expression as well as the TGFβ1-induced epithelial–mesenchymal transition phenomenon [55, 56]. In this study, we found that miR-378 transfection notably intensified the expression of TGFβ1, which could play a crucial role in promoting MSC differentiation into blood vessels. It has been recently reported that crosstalk between PDGFβ and TGFβ1 pathways is essential for mediating MSC mechanics and matrix interactions . Both PDGFβ and TGFβ1 were discovered to be increased in MSCs transfected with miR-378. Therefore, we inferred that TGFβ1 in combination with PDGF might further amplify the formation of vasculature in a hypoxic–ischemic environment.
There are some limitations to this study. MSCs without transfection were applied as the negative control; experiments using scrambled miRNA as a control for the miR-378 transfection would further be performed to eliminate nonspecific effects of transfection and make the data more convincing. As this study was conducted in vitro, the affection of miR-378 on MSCs in vivo is still lacking. How miR-378 could act on MSCs survival and differentiation in the injured heart in animal models would be further explored in our later work. In addition, although several molecules that might possibly participate in promoting MSCs survival after miR-378 transfection have been investigated in this paper, the elaborate downstream signaling pathways implicated should be searched for in the future studies in order to clarify the underlying mechanisms of the biological functions of miR-378.
In summary, this study showed that miR-378 could promote MSCs survival and the cells’ ability of vascularization under hypoxic–ischemic conditions in vitro. miR-378 might function on apoptosis-related and angiogenesis-related genes. Further explorations of the implications of miR-378 on MSCs in vivo will provide new mentalities for the treatment of ischemic heart disease based on MSCs transplantation.
mesenchymal stem cell
platelet-derived growth factor
real-time polymerase chain reaction
transforming growth factor beta-1
tumor necrosis factor alpha
vascular endothelial growth factor.
Hou J, Wang L, Jiang J, Zhou C, Guo T, Zheng S, Wang T: Cardiac stem cells and their roles in myocardial infarction. Stem Cell Rev. 2013, 9: 326-338. 10.1007/s12015-012-9421-4.
Chavakis E, Koyanagi M, Dimmeler S: Enhancing the outcome of cell therapy for cardiac repair progress from bench to bedside and back. Circulation. 2010, 121: 325-335. 10.1161/CIRCULATIONAHA.109.901405.
Wang T, Tang W, Sun S, Wan Z, Xu T, Huang Z, Weil MH: Mesenchymal stem cells improve outcomes of cardiopulmonary resuscitation in myocardial infarcted rats. J Mol Cell Cardiol. 2009, 46: 378-384. 10.1016/j.yjmcc.2008.11.014.
Hare JM, Fishman JE, Gerstenblith G, Velazquez DLD, Zambrano JP, Suncion VY, Tracy M, Ghersin E, Johnston PV, Brinker JA: Comparison of allogeneic vs autologous bone marrow–derived mesenchymal stem cells delivered by transendocardial injection in patients with ischemic cardiomyopathy: The POSEIDON Randomized Trial Mesenchymal Stem Cells and Ischemic Cardiomyopathy. JAMA. 2012, 308: 2369-2379. 10.1001/jama.2012.25321.
Mathiasen AB, Jørgensen E, Qayyum AA, Haack-Sørensen M, Ekblond A, Kastrup J: Rationale and design of the first randomized, double-blind, placebo-controlled trial of intramyocardial injection of autologous bone-marrow derived Mesenchymal Stromal Cells in chronic ischemic Heart Failure (MSC-HF Trial). Am Heart J. 2012, 164: 285-291. 10.1016/j.ahj.2012.05.026.
Wen Z, Zheng S, Zhou C, Wang J, Wang T: Repair mechanisms of bone marrow mesenchymal stem cells in myocardial infarction. J Cell Mol Med. 2011, 15: 1032-1043. 10.1111/j.1582-4934.2010.01255.x.
Williams AR, Hare JM: Mesenchymal stem cells biology, pathophysiology, translational findings, and therapeutic implications for cardiac disease. Circ Res. 2011, 109: 923-940. 10.1161/CIRCRESAHA.111.243147.
Wang T, Sun S, Wan Z, Weil MH, Tang W: Effects of bone marrow mesenchymal stem cells in a rat model of myocardial infarction. Resuscitation. 2012, 83: 1391-1396. 10.1016/j.resuscitation.2012.02.033.
Figeac F, Lesault PF, Coz O, Damy T, Souktani R, Trébeau C, Schmitt A, Ribot J, Mounier R, Guguin A: Nanotubular crosstalk with distressed cardiomyocytes stimulates the paracrine repair function of mesenchymal stem cells. Stem Cells. 2014, 32: 216-230. 10.1002/stem.1560.
Lee RH, Oh JY, Choi H, Bazhanov N: Therapeutic factors secreted by mesenchymal stromal cells and tissue repair. J Cell Biochem. 2011, 112: 3073-3078. 10.1002/jcb.23250.
Trachtenberg B, Velazquez DL, Williams AR, McNiece I, Fishman J, Nguyen K, Rouy D, Altman P, Schwarz R, Mendizabal A: Rationale and design of the Transendocardial Injection of Autologous Human Cells (bone marrow or mesenchymal) in Chronic Ischemic Left Ventricular Dysfunction and Heart Failure Secondary to Myocardial Infarction (TAC-HFT) trial: a randomized, double-blind, placebo-controlled study of safety and efficacy. Am Heart J. 2011, 161: 487-493. 10.1016/j.ahj.2010.11.024.
Hare JM, Traverse JH, Henry TD, Dib N, Strumpf RK, Schulman SP, Gerstenblith G, DeMaria AN, Denktas AE, Gammon RS: A randomized, double-blind, placebo-controlled, dose-escalation study of intravenous adult human mesenchymal stem cells (prochymal) after acute myocardial infarction. J Am Coll Cardiol. 2009, 54: 2277-2286. 10.1016/j.jacc.2009.06.055.
Copland IB, Lord-Dufour S, Cuerquis J, Coutu DL, Annabi B, Wang E, Galipeau J: Improved autograft survival of mesenchymal stromal cells by plasminogen activator inhibitor 1 inhibition. Stem Cells. 2009, 27: 467-477. 10.1634/stemcells.2008-0520.
McGinley LM, McMahon J, Stocca A, Duffy A, Flynn A, O'Toole D, O'Brien T: Mesenchymal stem cell survival in the infarcted heart is enhanced by lentivirus vector-mediated heat shock protein 27 expression. Hum Gene Ther. 2013, 24: 840-851. 10.1089/hum.2011.009.
Zhu W, Chen J, Cong X, Hu S, Chen X: Hypoxia and serum deprivation‒induced apoptosis in mesenchymal stem cells. Stem Cells. 2006, 24: 416-425. 10.1634/stemcells.2005-0121.
Hou M, Liu J, Liu F, Liu K, Yu B: C1q tumor necrosis factor-related protein-3 protects mesenchymal stem cells against hypoxia-and serum deprivation-induced apoptosis through the phosphoinositide 3-kinase/Akt pathway. Int J Mol Med. 2014, 33: 97-104.
Bartel DP: MicroRNAs: target recognition and regulatory functions. Cell. 2009, 136: 215-233. 10.1016/j.cell.2009.01.002.
Nie Y, Han B-M, Liu X-B, Yang J-J, Wang F, Cong X-F, Chen X: Identification of MicroRNAs involved in hypoxia-and serum deprivation-induced apoptosis in mesenchymal stem cells. Int J Biol Sci. 2011, 7: 762-768.
Huang F, Zhu X, Hu X-Q, Fang Z-F, Tang L, Lu X-L, Zhou S-H: Mesenchymal stem cells modified with miR-126 release angiogenic factors and activate Notch ligand Delta-like-4, enhancing ischemic angiogenesis and cell survival. Int J Mol Med. 2013, 31: 484-492.
Wen Z, Zheng S, Zhou C, Yuan W, Wang J, Wang T: Bone marrow mesenchymal stem cells for post‒myocardial infarction cardiac repair: micrornas as novel regulators. J Cell Mol Med. 2012, 16: 657-671. 10.1111/j.1582-4934.2011.01471.x.
Lee DY, Deng Z, Wang C-H, Yang BB: MicroRNA-378 promotes cell survival, tumor growth, and angiogenesis by targeting SuFu and Fus-1 expression. Proc Nat Acad Sci U S A. 2007, 104: 20350-20355. 10.1073/pnas.0706901104.
Kim SW, Kim HW, Huang W, Okada M, Welge JA, Wang Y, Ashraf M: Cardiac stem cells with electrical stimulation improve ischaemic heart function through regulation of connective tissue growth factor and miR-378. Cardiovasc Res. 2013, 100: 241-251. 10.1093/cvr/cvt192.
Fang J, Song X-W, Tian J, Chen H-Y, Li D-F, Wang J-F, Ren A-J, Yuan W-J, Lin L: Overexpression of microRNA-378 attenuates ischemia-induced apoptosis by inhibiting caspase-3 expression in cardiac myocytes. Apoptosis. 2012, 17: 410-423. 10.1007/s10495-011-0683-0.
Knezevic I, Patel A, Sundaresan NR, Gupta MP, Solaro RJ, Nagalingam RS, Gupta M: A novel cardiomyocyte-enriched MicroRNA, miR-378, targets insulin-like growth factor 1 receptor implications in postnatal cardiac remodeling and cell survival. J Biol Chem. 2012, 287: 12913-12926. 10.1074/jbc.M111.331751.
Nagalingam RS, Sundaresan NR, Gupta MP, Geenen DL, Solaro RJ, Gupta M: A cardiac-enriched microRNA, miR-378, blocks cardiac hypertrophy by targeting Ras signaling. J Biol Chem. 2013, 288: 11216-11232. 10.1074/jbc.M112.442384.
Prasad SVN, Duan Z-H, Gupta MK, Surampudi VSK, Volinia S, Calin GA, Liu C-G, Kotwal A, Moravec CS, Starling RC: Unique microRNA profile in end-stage heart failure indicates alterations in specific cardiovascular signaling networks. J Biol Chem. 2009, 284: 27487-27499. 10.1074/jbc.M109.036541.
Wang T, Tang W, Sun S, Ristagno G, Huang Z, Weil MH: Intravenous infusion of bone marrow mesenchymal stem cells improves myocardial function in a rat model of myocardial ischemia. Crit Care Med. 2007, 35: 2587-2593. 10.1097/01.CCM.0000285992.99391.7E.
Brill A, Dashevsky O, Rivo J, Gozal Y, Varon D: Platelet-derived microparticles induce angiogenesis and stimulate post-ischemic revascularization. Cardiovasc Res. 2005, 67: 30-38. 10.1016/j.cardiores.2005.04.007.
Wang S, Qu X, Zhao RC: Clinical applications of mesenchymal stem cells. J Hematol Oncol. 2012, 5: 19-10.1186/1756-8722-5-19.
Wang J, Li Z, Zhang Y, Liu X, Chen L, Chen Y: CX43 change in LPS preconditioning against apoptosis of mesenchymal stem cells induced by hypoxia and serum deprivation is associated with ERK signaling pathway. Mol Cell Biochem. 2013, 380: 267-275. 10.1007/s11010-013-1683-x.
Zhang Q, Yang Y-J, Wang H, Dong Q-T, Wang T-J, Qian H-Y, Xu H: Autophagy activation: a novel mechanism of atorvastatin to protect mesenchymal stem cells from hypoxia and serum deprivation via AMP-activated protein kinase/mammalian target of rapamycin pathway. Stem Cells Dev. 2012, 21: 1321-1332. 10.1089/scd.2011.0684.
Huang F, Li M-L, Fang Z-F, Hu X-Q, Liu Q-M, Liu Z-J, Tang L, Zhao Y-S, Zhou S-H: Overexpression of MicroRNA-1 improves the efficacy of mesenchymal stem cell transplantation after myocardial infarction. Cardiology. 2013, 125: 18-30. 10.1159/000347081.
Ouyang YB, Giffard RG: microRNAs affect BCL-2 family proteins in the setting of cerebral ischemia. Neurochem Int. 2014, 77: 2-8.
Ji L, Roth JA: Tumor suppressor FUS1 signaling pathway. J Thorac Oncol. 2008, 3: 327-10.1097/JTO.0b013e31816bce65.
Mao J, Lv Z, Zhuang Y: MicroRNA-23a is involved in tumor necrosis factor-α induced apoptosis in mesenchymal stem cells and myocardial infarction. Exp Mol Pathol. 2014, 97: 23-30. 10.1016/j.yexmp.2013.11.005.
Peng C-F, Han Y-L, Yan C-H: Overexpression of cellular repressor of E1A-stimulated genes inhibits TNF-α-induced apoptosis via NF-κB in mesenchymal stem cells. Biochem Biophys Res Commun. 2011, 406: 601-607. 10.1016/j.bbrc.2011.02.100.
Poynter JA, Herrmann JL, Manukyan MC, Wang Y, Abarbanell AM, Weil BR, Brewster BD, Meldrum DR: Intracoronary mesenchymal stem cells promote postischemic myocardial functional recovery, decrease inflammation, and reduce apoptosis via a signal transducer and activator of transcription 3 mechanism. J Am Coll Surg. 2011, 213: 253-260. 10.1016/j.jamcollsurg.2011.04.005.
Collino F, Bruno S, Deregibus MC, Tetta C, Camussi G: MicroRNAs and mesenchymal stem cells. Vitam Horm. 2011, 87: 291-320.
L-l Z, J-j L, Liu F, W-h L, Wang Y-s, Zhu B, Yu B: MiR-499 induces cardiac differentiation of rat mesenchymal stem cells through wnt/β-catenin signaling pathway. Biochem Biophys Res Commun. 2012, 420: 875-881. 10.1016/j.bbrc.2012.03.092.
Bonauer A, Boon RA, Dimmeler S: Vascular micrornas. Curr Drug Targets. 2010, 11: 943-949. 10.2174/138945010791591313.
Wang S, Olson EN: AngiomiRs – key regulators of angiogenesis. Curr Opin Gene Dev. 2009, 19: 205-211. 10.1016/j.gde.2009.04.002.
Yang J, Zhou W, Zheng W, Ma Y, Lin L, Tang T, Liu J, Yu J, Zhou X, Hu J: Effects of myocardial transplantation of marrow mesenchymal stem cells transfected with vascular endothelial growth factor for the improvement of heart function and angiogenesis after myocardial infarction. Cardiology. 2006, 107: 17-29.
Kim SH, Moon H-H, Kim HA, Hwang K-C, Lee M, Choi D: Hypoxia-inducible vascular endothelial growth factor-engineered mesenchymal stem cells prevent myocardial ischemic injury. Mol Ther. 2011, 19: 741-750. 10.1038/mt.2010.301.
Penna C, Perrelli MG, Karam JP, Angotti C, Muscari C, Montero‒Menei CN, Pagliaro P: Pharmacologically active microcarriers influence VEGF‒A effects on mesenchymal stem cell survival. J Cell Mol Med. 2013, 17: 192-204. 10.1111/j.1582-4934.2012.01662.x.
Skrzypek K, Tertil M, Golda S, Ciesla M, Weglarczyk K, Collet G, Guichard A, Kozakowska M, Boczkowski J, Was H: Interplay between heme oxygenase-1 and miR-378 affects non-small cell lung carcinoma growth, vascularization, and metastasis. Antioxid Redox Signal. 2013, 19: 644-660. 10.1089/ars.2013.5184.
Guiducci S, Manetti M, Romano E, Mazzanti B, Ceccarelli C, Dal Pozzo S, Milia AF, Bellando-Randone S, Fiori G, Conforti ML: Bone marrow-derived mesenchymal stem cells from early diffuse systemic sclerosis exhibit a paracrine machinery and stimulate angiogenesis in vitro. Ann Rheum Dis. 2011, 70: 2011-2021. 10.1136/ard.2011.150607.
Ball S, Worthington J, Canfield A, Merry C, Kielty C: Mesenchymal stromal cells: inhibiting PDGF receptors or depleting fibronectin induces mesodermal progenitors with endothelial potential. Stem Cells. 2014, 32: 694-705. 10.1002/stem.1538.
Ho IA, Toh HC, Ng WH, Teo YL, Guo CM, Hui KM, Lam PY: Human bone marrow‒derived mesenchymal stem cells suppress human glioma growth through inhibition of angiogenesis. Stem Cells. 2013, 31: 146-155. 10.1002/stem.1247.
Zhang J, Chintalgattu V, Shih T, Ai D, Xia Y, Khakoo AY: MicroRNA-9 is an activation-induced regulator of PDGFR-beta expression in cardiomyocytes. J Mol Cell Cardiol. 2011, 51: 337-346. 10.1016/j.yjmcc.2011.05.019.
Böttner M, Krieglstein K, Unsicker K: The transforming growth factor‒βs. J Neurochem. 2000, 75: 2227-2240.
Zhao L, Hantash BM: TGF-β1 regulates differentiation of bone marrow mesenchymal stem cells. Vitam Horm. 2011, 87: 127-141.
Kurpinski K, Chu J, Wang D, Li S: Proteomic profiling of mesenchymal stem cell responses to mechanical strain and TGF-beta1. Cell Mol Bioeng. 2009, 2: 606-614. 10.1007/s12195-009-0090-6.
Zhen G, Wen C, Jia X, Li Y, Crane JL, Mears SC, Askin FB, Frassica FJ, Chang W, Yao J: Inhibition of TGF-[beta] signaling in mesenchymal stem cells of subchondral bone attenuates osteoarthritis. Nat Med. 2013, 19: 704-712. 10.1038/nm.3143.
Kato M: TGF-β-induced signaling circuit loops mediated by microRNAs as new therapeutic targets for renal fibrosis?. Kidney Int. 2013, 84: 1067-1069. 10.1038/ki.2013.297.
Kitamura K, Seike M, Okano T, Matsuda K, Miyanaga A, Mizutani H, Noro R, Minegishi Y, Kubota K, Gemma A: MiR-134/487b/655 cluster regulates TGF-β-induced epithelial–mesenchymal transition and drug resistance to gefitinib by targeting MAGI2 in lung adenocarcinoma cells. Mol Cancer Ther. 2014, 13: 444-453. 10.1158/1535-7163.MCT-13-0448.
Sun X, He Y, Ma T-T, Huang C, Zhang L, Li J: Participation of miR-200a in TGF-β1-mediated hepatic stellate cell activation. Mol Cell Biochem. 2014, 388: 11-23. 10.1007/s11010-013-1895-0.
Ghosh D, Lili L, McGrail DJ, Matyunina LV, McDonald JF, Dawson MR: Integral role of platelet-derived growth factor in mediating transforming growth factor-β1–dependent mesenchymal stem cell stiffening. Stem Cells Dev. 2014, 23: 245-261. 10.1089/scd.2013.0240.
This study was supported by National Natural Science Foundation of China (No: 81070125, 81270213), the Science and Technology Foundation in Guangdong Province (No: 2010B031600032) and the Fundamental Research Funds for the Central Universities (13ykzd16).
This work was done by the investigators of the Sun Yat-sen Memorial Hospital of Sun Yat-sen University. The authors took responsibility for all aspects of the reliability and had no differences in data presentation and interpretation.
The authors declare that they have no competing interests.
YX, JH and TG carried out the cell culture and transfection, participated in the statistical analysis and drafted the manuscript. SZ and CZ carried out the tube formation assay and molecular assay. HH, YC, KS, TZ and JW participated in the technical assistance and statistical analysis. HL and TW conceived the study and participated in the study design. All authors read and approved the final manuscript.
Yue Xing, Jingying Hou, Tianzhu Guo contributed equally to this work.
About this article
Cite this article
Xing, Y., Hou, J., Guo, T. et al. microRNA-378 promotes mesenchymal stem cell survival and vascularization under hypoxic–ischemic conditions in vitro. Stem Cell Res Ther 5, 130 (2014). https://doi.org/10.1186/scrt520
- Vascular Endothelial Growth Factor
- Hypoxic Condition
- Human Umbilical Vein Endothelial Cell
- Hypoxia Exposure
- Bone Marrow Mesenchymal Stem Cell