4.5 Article

SRF-MRTF signaling suppresses brown adipocyte development by modulating TGF-β/BMP pathway

期刊

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2020.110920

关键词

Serum response factor; Myocardin-related transcription factors; Actin cytoskeleton; Brown adipogenesis

资金

  1. National Institutes of Health [DK097160-01, 1R01DK112794]
  2. American Heart Association [19CDA34770034, 17GRNT33370012]

向作者/读者索取更多资源

The SRF/MRTF and upstream signaling cascade play key roles in actin cytoskeleton organization and myocyte development. To date, how this signaling axis may function in brown adipocyte lineage commitment and maturation has not been delineated. Here we report that MRTF-SRF signaling exerts inhibitory actions on brown adipogenesis, and suppressing this negative regulation promotes brown adipocyte lineage development. During brown adipogenic differentiation, protein expressions of SRF, MRTFA/B and its transcription targets were downregulated, and MRTFA/B shuttled from nucleus to cytoplasm. Silencing of SRF or MRTF-A/MRTF-B enhanced two distinct stages of brown adipocyte development, mesenchymal stem cell determination to brown adipocytes and terminal differentiation of brown adipogenic progenitors. We further demonstrate that the MRTF-SRF axis exerts transcriptional regulations of the TGF-beta and BMP signaling pathway, critical developmental cues for brown adipocyte development. TGF-beta signaling activity was significantly attenuated, whereas that of the BMP pathway augmented by inhibition of SRF or MRTF-A/MRTF-B, leading to enhanced brown adipocyte differentiation. Our study demonstrates the MRTF-SRF transcriptional cascade as a negative regulator of brown adipogenesis, through its transcriptional control of the TGF-beta/BMP signaling pathways.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据