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IL-27 signalling promotes adipocyte thermogenesis and energy expenditure.

Qian WangDehai LiGuangchao CaoQiping ShiJing ZhuMingyue ZhangHao ChengQiong WenHao XuLeqing ZhuHua ZhangRachel J PerryOlga SpadaroYunfan YangShengqi HeYong ChenBaocheng WangGuangqiang LiZonghua LiuCaixian YangXiaoli WuLibing ZhouQinghua ZhouZhenyu JuHongyun LuYongjie XinXiaoyong YangCunchuan WangYong LiuGerald I ShulmanVishwa Deep DixitLigong LuHengwen YangRichard A FlavellZhinan Yin
Published in: Nature (2021)
Thermogenesis in brown and beige adipose tissue has important roles in maintaining body temperature and countering the development of metabolic disorders such as obesity and type 2 diabetes1,2. Although much is known about commitment and activation of brown and beige adipose tissue, its multiple and abundant immunological factors have not been well characterized3-6. Here we define a critical role of IL-27-IL-27Rα signalling in improving thermogenesis, protecting against diet-induced obesity and ameliorating insulin resistance. Mechanistic studies demonstrate that IL-27 directly targets adipocytes, activating p38 MAPK-PGC-1α signalling and stimulating the production of UCP1. Notably, therapeutic administration of IL-27 ameliorated metabolic morbidities in well-established mouse models of obesity. Consistently, individuals with obesity show significantly decreased levels of serum IL-27, which can be restored after bariatric surgery. Collectively, these findings show that IL-27 has an important role in orchestrating metabolic programs, and is a highly promising target for anti-obesity immunotherapy.
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