5-Azacytidine Induces Cardiac Differentiation of Human Umbilical Cord-Derived Mesenchymal Stem Cells by Activating Extracellular Regulated Kinase

被引:120
作者
Qian, Qian [1 ]
Qian, Hui [1 ]
Zhang, Xu [1 ]
Zhu, Wei [1 ]
Yan, Yongmin [1 ]
Ye, Shengqin [2 ]
Peng, Xiujuan [1 ]
Li, Wei [2 ]
Xu, Zhe [1 ]
Sun, Lingyun [3 ]
Xu, Wenrong [1 ]
机构
[1] Jiangsu Univ, Sch Med Sci & Lab Med, Zhenjiang 212013, Peoples R China
[2] Jiangsu Ctr Stem Cell Engn & Technol, Taizhou, Peoples R China
[3] Nanjing Univ, Sch Med, Affiliated Drum Tower Hosp, Dept Immunol & Rheumatol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MARROW STROMAL CELLS; BONE-MARROW; SERINE PHOSPHORYLATION; GENE-EXPRESSION; IN-VITRO; CARDIOMYOCYTES; GROWTH; PROLIFERATION; REGENERATION; STAT3;
D O I
10.1089/scd.2010.0519
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
5-Azacytidine (5-Aza) induces differentiation of mesenchymal stem cells (MSCs) into cardiomyocytes. However, the underlying mechanisms are not well understood. Our previous work showed that 5-Aza induces human bone marrow-derived MSCs to differentiate into cardiomyocytes. Here, we demonstrated that 5-Aza induced cardiac differentiation of human umbilical cord-derived MSCs (hucMSCs) and explored the potential signaling pathway. Our results showed that hucMSCs had cardiomyocyte phenotypes after 5-Aza treatment. In addition, myogenic cells differentiated from hucMSCs were positive for mRNA and protein of desmin, beta-myosin heavy chain, cardiac troponin T, A-type natriuretic peptide, and Nkx2.5. Human diploid lung fibroblasts treated with 5-Aza expressed no cardiac-specific genes. 5-Aza did not induce hucMSCs to differentiate into osteoblasts. Further study revealed that 5-Aza treatment activated extracellular signal related kinases (ERK) in hucMSCs, but protein kinase C showed no response to 5-Aza administration. U0126, a specific inhibitor of ERK, could inhibit 5-Aza-induced expression of cardiac-specific genes and proteins in hucMSCs. Increased phosphorylation of signal transducers and activators of transcription 3, and up-regulation of myocyte enhancer-binding factor-2c and myogenic differentiation antigen in 5-Aza-treated hucMSCs were also suppressed by U0126. Taken together, these results suggested that sustained activation of ERK by 5-Aza contributed to the induction of the differentiation of hucMSCs into cardiomyocytes in vitro.
引用
收藏
页码:67 / 75
页数:9
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