Volume 34, Issue 4 pp. 283-289
Original Research Article
Free to Read

Resveratrol promotes differentiation of mouse embryonic stem cells to cardiomyocytes

Hong Ding

Hong Ding

Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China

Contributed equally.Search for more papers by this author
Xin Xu

Xin Xu

Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China

Contributed equally.Search for more papers by this author
Xian Qin

Xian Qin

Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China

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Chengjian Yang

Corresponding Author

Chengjian Yang

Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China

Correspondence

C. Yang and Q. Feng, Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China.

Email: [email protected] and [email protected]

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Qiuting Feng

Corresponding Author

Qiuting Feng

Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China

Correspondence

C. Yang and Q. Feng, Department of Cardiology, Affiliated Hospital of Nanjing Medical University, Wuxi No. 2 People's Hospital, Wuxi, Jiangsu, China.

Email: [email protected] and [email protected]

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First published: 26 May 2016
Citations: 18

Summary

Aim

Embryonic stem cells (ESCs) are capable to differentiate into cardiomyocytes, with the potential to treat cardiovascular diseases. However, directed differentiation is still a challenge faced by scientists. As a natural substance in grapes, resveratrol (RV) is important for cardiovascular protection. The studies of RV and its effects on ESC differentiation have potential clinical applications.

Methods

Using mouse embryonic stem cells (mESCs), we investigated the effects of different concentrations of RV (5, 10, 20, 50, and 100 μmol/L) exposure on mESCs viability, expression levels of cardiac marker genes in embryoid bodies (EBs) derived from mESCs, expression levels of maturity indicative cardiac markers in cardiomyocytes derived from mESCs, and the beating properties of EBs.

Results

About 10 μmol/L of RV showed no toxicity on cell viability and was the optimal concentration to promote mESC differentiation, induce mESC differentiation to cardiomyocytes, and gain the beating properties of EBs.

Conclusion

RV can successfully direct the differentiation of mESCs into cardiomyocytes, shedding light on its future applications to treat cardiovascular diseases.

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