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Inefficient reprogramming of fibroblasts into cardiomyocytes using Gata4, Mef2c, and Tbx5.使用 Gata4、Mef2c 和 Tbx5 将成纤维细胞低效重编程为心肌细胞。
Circ Res. 2012 Jun 22;111(1):50-5. doi: 10.1161/CIRCRESAHA.112.270264. Epub 2012 May 10.
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Production of de novo cardiomyocytes: human pluripotent stem cell differentiation and direct reprogramming.生成新的心肌细胞:人类多能干细胞的分化和直接重编程。
Cell Stem Cell. 2012 Jan 6;10(1):16-28. doi: 10.1016/j.stem.2011.12.013.
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GATA5 interacts with GATA4 and GATA6 in outflow tract development.GATA5 与 GATA4 和 GATA6 在流出道发育中相互作用。
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Fgf differentially controls cross-antagonism between cardiac and haemangioblast regulators.Fgf 差异调控心脏和血岛形成细胞调节因子的交叉拮抗作用。
Development. 2011 Aug;138(15):3235-45. doi: 10.1242/dev.059634.
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Smarcd3b and Gata5 promote a cardiac progenitor fate in the zebrafish embryo.Smarcd3b 和 Gata5 在斑马鱼胚胎中促进心脏祖细胞命运。
Development. 2011 Aug;138(15):3113-23. doi: 10.1242/dev.064279. Epub 2011 Jun 29.
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Stage-specific optimization of activin/nodal and BMP signaling promotes cardiac differentiation of mouse and human pluripotent stem cell lines.阶段特异性激活素/ nodal 和 BMP 信号转导促进小鼠和人多能干细胞系的心脏分化。
Cell Stem Cell. 2011 Feb 4;8(2):228-40. doi: 10.1016/j.stem.2010.12.008.
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Mesp1: a key regulator of cardiovascular lineage commitment.Mesp1:心血管谱系决定的关键调节因子。
Circ Res. 2010 Dec 10;107(12):1414-27. doi: 10.1161/CIRCRESAHA.110.227058.
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Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors.通过定义因子将成纤维细胞直接重编程为功能性心肌细胞。
Cell. 2010 Aug 6;142(3):375-86. doi: 10.1016/j.cell.2010.07.002.
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The cooperative roles of Foxc1 and Foxc2 in cardiovascular development.Foxc1 和 Foxc2 在心血管发育中的协同作用。
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Gata4 and Gata5 cooperatively regulate cardiac myocyte proliferation in mice.Gata4 和 Gata5 协同调节小鼠心肌细胞的增殖。
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GATA 因子能有效地将胚胎干细胞定向分化为心脏细胞。

GATA factors efficiently direct cardiac fate from embryonic stem cells.

机构信息

Department of Surgery, Weill Cornell Medical College, New York, NY 10065, USA.

出版信息

Development. 2013 Apr;140(8):1639-44. doi: 10.1242/dev.093260. Epub 2013 Mar 13.

DOI:10.1242/dev.093260
PMID:23487308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3621482/
Abstract

The GATA4 transcription factor is implicated in promoting cardiogenesis in combination with other factors, including TBX5, MEF2C and BAF60C. However, when expressed in embryonic stem cells (ESCs), GATA4 was shown to promote endoderm, not cardiac mesoderm. The capacity of related GATA factors to promote cardiogenesis is untested. We found that expression of the highly related gene, Gata5, very efficiently promotes cardiomyocyte fate from murine ESCs. Gata5 directs development of beating sheets of cells that express cardiac troponin T and show a full range of action potential morphologies that are responsive to pharmacological stimulation. We discovered that by removing serum from the culture conditions, GATA4 and GATA6 are each also able to efficiently promote cardiogenesis in ESC derivatives, with some distinctions. Thus, GATA factors can function in ESC derivatives upstream of other cardiac transcription factors to direct the efficient generation of cardiomyocytes.

摘要

GATA4 转录因子与其他因子(包括 TBX5、MEF2C 和 BAF60C)结合,被认为能促进心脏发生。然而,在胚胎干细胞(ESCs)中表达时,GATA4 被证明能促进内胚层,而不是心脏中胚层的发生。相关 GATA 因子促进心脏发生的能力尚未得到测试。我们发现,高度相关的基因 Gata5 的表达非常有效地促进了来自小鼠 ESCs 的心肌细胞命运。Gata5 指导形成表达心肌肌钙蛋白 T 的搏动细胞片层,并表现出对药物刺激有反应的全范围动作电位形态。我们发现,通过从培养条件中去除血清,GATA4 和 GATA6 各自也能够有效地促进 ESC 衍生物中的心脏发生,存在一些区别。因此,GATA 因子可以在 ESC 衍生物中的其他心脏转录因子之前发挥作用,以指导心肌细胞的有效生成。