Literature DB >> 32603734

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

Ruya Liu1, Xuekai Xiong2, Deokhwa Nam3, Vijay Yechoor4, Ke Ma5.   

Abstract

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 down-regulated, 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-β and BMP signaling pathway, critical developmental cues for brown adipocyte development. TGF-β 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-β/BMP signaling pathways.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

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

Mesh:

Substances:

Year:  2020        PMID: 32603734      PMCID: PMC7484394          DOI: 10.1016/j.mce.2020.110920

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


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