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Control of murine brown adipocyte development by GATA6

  • Seoyoung Jun
  • , Anthony R. Angueira
  • , Ethan C. Fein
  • , Josephine M.E. Tan
  • , Angela H. Weller
  • , Lan Cheng
  • , Kirill Batmanov
  • , Jeff Ishibashi
  • , Alexander P. Sakers
  • , Rachel R. Stine
  • , Patrick Seale*
  • *Corresponding author for this work
  • University of Pennsylvania

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Brown adipose tissue (BAT) is a thermogenic organ that protects animals against hypothermia and obesity. BAT derives from the multipotent paraxial mesoderm; however, the identity of embryonic brown fat progenitor cells and regulators of adipogenic commitment are unclear. Here, we performed single-cell gene expression analyses of mesenchymal cells during mouse embryogenesis with a focus on BAT development. We identified cell populations associated with the development of BAT, including Dpp4+ cells that emerge at the onset of adipogenic commitment. Immunostaining and lineage-tracing studies show that Dpp4+ cells constitute the BAT fascia and contribute minorly as adipocyte progenitors. Additionally, we identified the transcription factor GATA6 as a marker of brown adipogenic progenitor cells. Deletion of Gata6 in the brown fat lineage resulted in a striking loss of BAT. Together, these results identify progenitor and transitional cells in the brown adipose lineage and define a crucial role for GATA6 in BAT development.

Original languageEnglish
Pages (from-to)2195-2205.e5
JournalDevelopmental Cell
Volume58
Issue number21
DOIs
Publication statusPublished - 6 Nov 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • adipose tissue
  • brown adipocyte
  • brown adipocyte development
  • brown adipogenesis
  • DPP4
  • EBF2
  • GATA6
  • progenitor
  • UCP1
  • Animals
  • Mice
  • Adipocytes, Brown/metabolism
  • Adipogenesis
  • Adipose Tissue, Brown/metabolism
  • Dipeptidyl Peptidase 4/metabolism
  • Obesity/metabolism
  • Thermogenesis/genetics

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