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通过Nkx2-5、Tbx5、Gata4和Myocd对哺乳动物非成肌细胞进行心脏基因激活分析。

Cardiac gene activation analysis in mammalian non-myoblasic cells by Nkx2-5, Tbx5, Gata4 and Myocd.

作者信息

Zhou Lei, Liu Yu, Lu Li, Lu Xinzheng, Dixon Richard A F

机构信息

Department of Molecular Cardiology, Texas Heart Institute, Houston, Texas, United States of America.

出版信息

PLoS One. 2012;7(10):e48028. doi: 10.1371/journal.pone.0048028. Epub 2012 Oct 29.

Abstract

Cardiac transcription factors are master regulators during heart development. Some were shown to transdifferentiate tail tip and cardiac fibroblasts into cardiomyocytes. However, recent studies have showed that controversies exist. Potential difference in tail tip and cardiac fibroblast isolation may possibly confound the observations. Moreover, due to the use of a cardiac reporter (Myh6) selection strategy for induced cardiomyocyte enrichment, and the lack of tracking signals for each transcription factors, individual roles of each transcription factors in activating cardiac gene expression in mammalian non-myoblastic cells have never been elucidated. Answers to these questions are an important step toward cardiomyocyte regeneration. Because mouse 10T1/2 fibroblasts are non-myoblastic in nature and can be induced to express genes of all three types of muscle cells, they are an ideal model for the analysis of cardiac and non-cardiac gene activation after induction. We constructed bi-cistronic lentiviral vectors, capable of expressing cardiac transcription factors along with different fluorescent tracking signals. By infecting 10T1/2 fibroblasts with Nkx2-5, Tbx5, Gata4 or Myocd cardiac transcription factor lentivirus alone or different combinations, we found that only Tbx5+Myocd and Tbx5+Gata4+Myocd combinations induced Myh6 and Tnnt2 cardiac marker protein expression. Microarray-based gene ontology analysis revealed that Tbx5 alone activated genes involved in the Wnt receptor signaling pathway and inhibited genes involved in a number of cardiac-related processes. Myocd alone activated genes involved in a number of cardiac-related processes and inhibited genes involved in the Wnt receptor signaling pathway and non-cardiac processes. Gata4 alone inhibited genes involved in non-cardiac processes. Tbx5+Gata4+Myocd was the most effective activator of genes associated with cardiac-related processes. Unlike Tbx5, Gata4, Myocd alone or Tbx5+Myocd, Tbx5+Gata4+Myocd activated the fewest genes associated with non-cardiac processes. Conclusively, Tbx5, Gata4 and Myocd play different roles in cardiac gene activation in mammalian non-myoblastic cells. Tbx5+Gata4+Myocd activates the most cardiac and the least non-cardiac gene expression.

摘要

心脏转录因子是心脏发育过程中的主要调节因子。一些研究表明,它们能将尾尖细胞和心脏成纤维细胞转分化为心肌细胞。然而,最近的研究表明存在争议。尾尖细胞和心脏成纤维细胞分离过程中的潜在差异可能会混淆观察结果。此外,由于使用心脏报告基因(Myh6)选择策略来富集诱导心肌细胞,且缺乏针对每个转录因子的追踪信号,每个转录因子在激活哺乳动物非成肌细胞中心脏基因表达的个体作用从未得到阐明。回答这些问题是心肌细胞再生的重要一步。由于小鼠10T1/2成纤维细胞本质上是非成肌细胞,并且可以被诱导表达所有三种类型肌肉细胞的基因,它们是分析诱导后心脏和非心脏基因激活的理想模型。我们构建了双顺反子慢病毒载体,能够表达心脏转录因子以及不同的荧光追踪信号。通过单独或不同组合用Nkx2-5、Tbx5、Gata4或Myocd心脏转录因子慢病毒感染10T1/2成纤维细胞,我们发现只有Tbx5+Myocd和Tbx5+Gata4+Myocd组合诱导了Myh6和Tnnt2心脏标志物蛋白的表达。基于微阵列的基因本体分析表明,单独的Tbx5激活了参与Wnt受体信号通路的基因,并抑制了参与许多心脏相关过程的基因。单独的Myocd激活了参与许多心脏相关过程的基因,并抑制了参与Wnt受体信号通路和非心脏过程的基因。单独的Gata4抑制了参与非心脏过程的基因。Tbx5+Gata4+Myocd是与心脏相关过程相关基因的最有效激活剂。与单独的Tbx5、Gata4、Myocd或Tbx5+Myocd不同,Tbx5+Gata4+Myocd激活的与非心脏过程相关的基因最少。总之,Tbx5、Gata4和Myocd在哺乳动物非成肌细胞的心脏基因激活中发挥不同作用。Tbx5+Gata4+Myocd激活的心脏基因表达最多,非心脏基因表达最少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0552/3483304/9eb80517f0b7/pone.0048028.g001.jpg

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