Lack of p38 activation in T cells increases IL-35 and protects against obesity by promoting thermogenesis

T细胞中p38激活不足会增加IL-35的表达,并通过促进产热作用来预防肥胖。

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作者:Ivana Nikolic # ,Irene Ruiz-Garrido # ,María Crespo ,Rafael Romero-Becerra ,Luis Leiva-Vega ,Alfonso Mora ,Marta León ,Elena Rodríguez ,Magdalena Leiva ,Ana Belén Plata-Gómez ,Maria Beatriz Alvarez Flores ,Jorge L Torres ,Lourdes Hernández-Cosido ,Juan Antonio López ,Jesús Vázquez ,Alejo Efeyan ,Pilar Martin ,Miguel Marcos ,Guadalupe Sabio

Abstract

Obesity is characterized by low-grade inflammation, energy imbalance and impaired thermogenesis. The role of regulatory T cells (Treg) in inflammation-mediated maladaptive thermogenesis is not well established. Here, we find that the p38 pathway is a key regulator of T cell-mediated adipose tissue (AT) inflammation and browning. Mice with T cells specifically lacking the p38 activators MKK3/6 are protected against diet-induced obesity, leading to an improved metabolic profile, increased browning, and enhanced thermogenesis. We identify IL-35 as a driver of adipocyte thermogenic program through the ATF2/UCP1/FGF21 pathway. IL-35 limits CD8+ T cell infiltration and inflammation in AT. Interestingly, we find that IL-35 levels are reduced in visceral fat from obese patients. Mechanistically, we demonstrate that p38 controls the expression of IL-35 in human and mouse Treg cells through mTOR pathway activation. Our findings highlight p38 signaling as a molecular orchestrator of AT T cell accumulation and function.

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