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胃饥饿素促进人胚胎干细胞向心肌细胞分化。

Ghrelin promotes differentiation of human embryonic stem cells into cardiomyocytes.

机构信息

Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing, China.

出版信息

Acta Pharmacol Sin. 2011 Oct;32(10):1239-45. doi: 10.1038/aps.2011.79. Epub 2011 Aug 1.

Abstract

AIM

Ghrelin is involved in regulating the differentiation of mesoderm-derived precursor cells. The aim of this study was to investigate whether ghrelin modulated the differentiation of human embryonic stem (hES) cells into cardiomyocytes and, if so, whether the effect was mediated by growth hormone secretagogue receptor 1α (GHS-R1α).

METHODS

Cardiomyocyte differentiation from hES cells was performed according to an embryoid body (EB)-based protocol. The cumulative percentage of beating EBs was calculated. The expression of cardiac-specific markers including cardiac troponin I (cTnI) and α-myosin heavy chain (α-MHC) was detected using RT-PCR, real-time PCR and Western blot. The dispersed beating EBs were examined using immunofluorescent staining.

RESULTS

The percentage of beating EBs and the expression of cTnI were significantly increased after ghrelin (0.1 and 1 nmol/L) added into the differentiation medium. From 6 to 18 d of differentiation, the increased expression of cTnI and α-MHC by ghrelin (1 nmol/L) was time-dependent, and in line with the alteration of the percentages of beating EBs. Furthermore, the dispersed beating EBs were double-positively immunostained with antibodies against cTnI and α-actinin. However, blockage of GHS-R1α with its specific antagonist D-[lys(3)]-GHRP-6 (1 μmol/L) did not alter the effects of ghrelin on cardiomyocyte differentiation.

CONCLUSION

Our data show that ghrelin enhances the generation of cardiomyocytes from hES cells, which is not mediated via GHS-R1α.

摘要

目的

Ghrelin 参与调节中胚层衍生前体细胞的分化。本研究旨在探讨 Ghrelin 是否调节人胚胎干细胞(hES)细胞向心肌细胞的分化,如果是,这种作用是否通过生长激素促分泌受体 1α(GHS-R1α)介导。

方法

根据胚状体(EB)为基础的方案进行 hES 细胞向心肌细胞的分化。计算搏动 EB 的累积百分比。使用 RT-PCR、实时 PCR 和 Western blot 检测心脏特异性标志物包括肌钙蛋白 I(cTnI)和α-肌球蛋白重链(α-MHC)的表达。使用免疫荧光染色检查分散的搏动 EB。

结果

Ghrelin(0.1 和 1 nmol/L)添加到分化培养基中后,搏动 EB 的百分比和 cTnI 的表达明显增加。在分化的第 6 天至第 18 天,Ghrelin(1 nmol/L)对 cTnI 和 α-MHC 的表达增加呈时间依赖性,与搏动 EB 的百分比变化一致。此外,分散的搏动 EB 与 cTnI 和 α-辅肌动蛋白的抗体双阳性免疫染色。然而,用其特异性拮抗剂 D-[lys(3)]-GHRP-6(1 μmol/L)阻断 GHS-R1α并不能改变 Ghrelin 对心肌细胞分化的影响。

结论

我们的数据表明 Ghrelin 增强了 hES 细胞向心肌细胞的生成,而这种作用不通过 GHS-R1α 介导。

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