Electrical Stimulation Enhances Cardiac Differentiation of Human Induced Pluripotent Stem Cells for Myocardial Infarction Therapy

被引:72
作者
Ma, Ruilian [1 ]
Liang, Jialiang [1 ]
Huang, Wei [1 ]
Guo, Linlin [1 ]
Cai, Wenfeng [1 ]
Wang, Lei [1 ]
Paul, Christian [1 ]
Yang, Huang-Tian [2 ,3 ,4 ]
Kim, Ha Won [1 ,5 ]
Wang, Yigang [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Pathol & Lab Med, 231 Albert Sabin Way, Cincinnati, OH 45267 USA
[2] Chinese Acad Sci, Inst Hlth Sci, Inst Biol Sci SIBS, Key Lab Stem Cell Biol, Shanghai, Peoples R China
[3] Chinese Acad Sci, Inst Hlth Sci, Inst Biol Sci SIBS, Lab Mol Cardiol, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med SJTUSM, Shanghai, Peoples R China
[5] Georgia Regents Univ, Dept Internal Med, Vasc Biol Ctr, Med Coll Georgia, Augusta, GA USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
induced pluripotent stem cells; cardiomyocytes; electric stimulation; cellular differentiation; myocardial infarction; calcium pathways; CARDIOMYOCYTE DIFFERENTIATION; MAGNETIC-FIELDS; CA2+ INFLUX; MYOCYTES; CALCIUM; GENERATION; MATURATION; PURIFICATION; ACTIVATION; EXPRESSION;
D O I
10.1089/ars.2016.6766
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aims: Electrical stimulation (EleS) can promote cardiac differentiation, but the underlying mechanism is not well known. This study investigated the effect of EleS on cardiomyocyte (CM) differentiation of human induced pluripotent stem cells (hiPSCs) and evaluated the therapeutic effects for the treatment of myocardial infarction (MI). Results: Cardiac differentiation of hiPSCs was induced with EleS after embryoid body formation. Spontaneously beating hiPSCs were observed as early at 2 days when treated with EleS compared with control treatment. The cardiac differentiation efficiency of hiPSCs was significantly enhanced by EleS. In addition, the functional maturation of hiPSC-CMs under EleS was confirmed by calcium indicators, intracellular Ca2+ levels, and expression of structural genes. Mechanistically, EleS mediated cardiac differentiation of hiPSCs through activation of Ca2+/PKC/ERK pathways, as revealed by RNA sequencing, quantitative polymerase chain reaction, and Western blotting. After transplantation in immunodeficient MI mice, EleS-preconditioned hiPSC-derived cells significantly improved cardiac function and attenuated expansion of infarct size. The preconditioned hiPSC-derived CMs were functionally integrated with the host heart. Innovation: We show EleS as an efficacious time-saving approach for CM generation. The global RNA profiling shows that EleS can accelerate cardiac differentiation of hiPSCs through activation of multiple pathways. The cardiac-mimetic electrical signals will provide a novel approach to generate functional CMs and facilitate cardiac tissue engineering for successful heart regeneration. Conclusion: EleS can enhance efficiency of cardiac differentiation in hiPSCs and promote CM maturation. The EleS-preconditioned CMs emerge as a promising approach for clinical application in MI treatment.
引用
收藏
页码:371 / 384
页数:14
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