| Literature DB >> 27568548 |
Svetlana Altshuler-Keylin1, Kosaku Shinoda1, Yutaka Hasegawa1, Kenji Ikeda1, Haemin Hong1, Qianqian Kang1, Yangyu Yang1, Rushika M Perera2, Jayanta Debnath3, Shingo Kajimura4.
Abstract
Beige adipocytes gained much attention as an alternative cellular target in anti-obesity therapy. While recent studies have identified a number of regulatory circuits that promote beige adipocyte differentiation, the molecular basis of beige adipocyte maintenance remains unknown. Here, we demonstrate that beige adipocytes progressively lose their morphological and molecular characteristics after withdrawing external stimuli and directly acquire white-like characteristics bypassing an intermediate precursor stage. The beige-to-white adipocyte transition is tightly coupled to a decrease in mitochondria, increase in autophagy, and activation of MiT/TFE transcription factor-mediated lysosome biogenesis. The autophagy pathway is crucial for mitochondrial clearance during the transition; inhibiting autophagy by uncoupled protein 1 (UCP1(+))-adipocyte-specific deletion of Atg5 or Atg12 prevents beige adipocyte loss after withdrawing external stimuli, maintaining high thermogenic capacity and protecting against diet-induced obesity and insulin resistance. The present study uncovers a fundamental mechanism by which autophagy-mediated mitochondrial clearance controls beige adipocyte maintenance, thereby providing new opportunities to counteract obesity.Entities:
Keywords: beige adipocytes; diabetes; mitochondria; mitophagy; obesity
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Year: 2016 PMID: 27568548 PMCID: PMC5023491 DOI: 10.1016/j.cmet.2016.08.002
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287