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Kindlin 2 通过经典 Wnt 信号通路在成肌分化过程中调节生肌相关因子(myogenin)。

Kindlin 2 regulates myogenic related factor myogenin via a canonical Wnt signaling in myogenic differentiation.

机构信息

Key Laboratory of Carcinogenesis and Translational Research, Ministry of Education of China, Peking University Health Science Center, Beijing, China.

出版信息

PLoS One. 2013 May 22;8(5):e63490. doi: 10.1371/journal.pone.0063490. Print 2013.

Abstract

Kindlin 2, as an integrin-associated protein, is required for myocyte elongation and fusion. However, the association of Kindlin 2 with muscle differentiation-related signaling pathways is unknown. Here, we identified a mechanism that Kindlin 2 regulates myogenic regulatory factors myogenin via a canonical Wnt/β-catenin signaling. We found that knockdown of Kindlin 2 leads to the abolishment of β-catenin/TCF4-mediated transcription in C2C12 cells, followed by the impairment of myogenic differentiation. Mechanistically, nuclear translocation of both Kindlin 2 and β-catenin is induced during myogenic differentiation. In particular, Kindlin 2 forms a tripartite complex with active β-catenin and TCF4, and hence co-occupied on the promoter of myogenin to enhance its expression. Functionally, depletion of Kindlin 2 impairs myogenic differentiation via downregulation of myogenin. Taken together, our data reveal that Kindlin 2 is required for Wnt signaling-regulated myogenic differentiation, providing a mechanistic insight into the role of Kindlin-2 in muscle development.

摘要

Kindlin 2 作为整合素相关蛋白,对于心肌细胞的伸长和融合是必需的。然而,Kindlin 2 与肌肉分化相关信号通路的关联尚不清楚。在这里,我们确定了一种机制,Kindlin 2 通过经典的 Wnt/β-catenin 信号通路调节肌生成调节因子 myogenin。我们发现,Kindlin 2 的敲低导致 C2C12 细胞中β-catenin/TCF4 介导的转录被废除,随后肌发生分化受损。在机制上,Kindlin 2 和β-catenin 在肌发生分化过程中均被诱导发生核转位。特别是,Kindlin 2 与活性β-catenin 和 TCF4 形成三元复合物,并因此共同占据 myogenin 的启动子以增强其表达。功能上,Kindlin 2 的耗竭通过下调 myogenin 来损害肌发生分化。总之,我们的数据揭示了 Kindlin 2 对于 Wnt 信号调节的肌发生分化是必需的,为 Kindlin-2 在肌肉发育中的作用提供了机制上的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba58/3661532/6709f63ed55d/pone.0063490.g001.jpg

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