| Literature DB >> 32615086 |
Yasuo Oguri1, Kosaku Shinoda2, Hyeonwoo Kim3, Diana L Alba4, W Reid Bolus4, Qiang Wang1, Zachary Brown5, Rachana N Pradhan5, Kazuki Tajima5, Takeshi Yoneshiro5, Kenji Ikeda6, Yong Chen7, Rachel T Cheang4, Kazuyuki Tsujino8, Caroline R Kim3, Vanille Juliette Greiner9, Ritwik Datta10, Christopher D Yang10, Kamran Atabai10, Michael T McManus9, Suneil K Koliwad4, Bruce M Spiegelman3, Shingo Kajimura11.
Abstract
Adipose tissues dynamically remodel their cellular composition in response to external cues by stimulating beige adipocyte biogenesis; however, the developmental origin and pathways regulating this process remain insufficiently understood owing to adipose tissue heterogeneity. Here, we employed single-cell RNA-seq and identified a unique subset of adipocyte progenitor cells (APCs) that possessed the cell-intrinsic plasticity to give rise to beige fat. This beige APC population is proliferative and marked by cell-surface proteins, including PDGFRα, Sca1, and CD81. Notably, CD81 is not only a beige APC marker but also required for de novo beige fat biogenesis following cold exposure. CD81 forms a complex with αV/β1 and αV/β5 integrins and mediates the activation of integrin-FAK signaling in response to irisin. Importantly, CD81 loss causes diet-induced obesity, insulin resistance, and adipose tissue inflammation. These results suggest that CD81 functions as a key sensor of external inputs and controls beige APC proliferation and whole-body energy homeostasis.Entities:
Keywords: adipocyte progenitors; adipogenesis; beige fat; brown fat; diabetes; metabolic adaptation; metabolic disease; metabolism; obesity; tissue remodeling
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Year: 2020 PMID: 32615086 PMCID: PMC7415677 DOI: 10.1016/j.cell.2020.06.021
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582