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

Mol Cell Endocrinol. 2020 Sep 15:515:110920. doi: 10.1016/j.mce.2020.110920. Epub 2020 Jun 27.

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.

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

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown / metabolism*
  • Adipogenesis / physiology
  • Animals
  • Bone Morphogenetic Protein Receptors / metabolism*
  • Cell Differentiation / physiology
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Cytoplasm / metabolism
  • Down-Regulation / physiology
  • Gene Expression Regulation / physiology
  • HEK293 Cells
  • Humans
  • Male
  • Mesenchymal Stem Cells / metabolism
  • Mice, Inbred C57BL
  • Serum Response Factor / metabolism*
  • Signal Transduction / physiology*
  • Trans-Activators / metabolism*
  • Transcription, Genetic / physiology
  • Transforming Growth Factor beta / metabolism*

Substances

  • Mrtfa protein, mouse
  • Serum Response Factor
  • Srf protein, mouse
  • Trans-Activators
  • Transforming Growth Factor beta
  • Bone Morphogenetic Protein Receptors