Institute of Food, Nutrition and Health, ETH Zürich, 8603, Schwerzenbach, Switzerland.
Institute of Experimental Endocrinology, Biomedical Research Center at the Slovak Academy of Sciences, 84505, Bratislava, Slovakia.
Nat Commun. 2021 Dec 8;12(1):7144. doi: 10.1038/s41467-021-27442-x.
Activation of thermogenic brown and beige adipocytes is considered as a strategy to improve metabolic control. Here, we identify GPR180 as a receptor regulating brown and beige adipocyte function and whole-body glucose homeostasis, whose expression in humans is associated with improved metabolic control. We demonstrate that GPR180 is not a GPCR but a component of the TGFβ signalling pathway and regulates the activity of the TGFβ receptor complex through SMAD3 phosphorylation. In addition, using genetic and pharmacological tools, we provide evidence that GPR180 is required to manifest Collagen triple helix repeat containing 1 (CTHRC1) action to regulate brown and beige adipocyte activity and glucose homeostasis. In this work, we show that CTHRC1/GPR180 signalling integrates into the TGFβ signalling as an alternative axis to fine-tune and achieve low-grade activation of the pathway to prevent pathophysiological response while contributing to control of glucose and energy metabolism.
棕色和米色脂肪细胞的激活被认为是改善代谢控制的一种策略。在这里,我们鉴定出 GPR180 是一种调节棕色和米色脂肪细胞功能和全身葡萄糖稳态的受体,其在人类中的表达与改善代谢控制有关。我们证明 GPR180 不是 GPCR,而是 TGFβ 信号通路的一个组成部分,通过 SMAD3 磷酸化调节 TGFβ 受体复合物的活性。此外,我们使用遗传和药理学工具提供证据表明,GPR180 是表现 Collagen triple helix repeat containing 1 (CTHRC1) 作用以调节棕色和米色脂肪细胞活性和葡萄糖稳态所必需的。在这项工作中,我们表明 CTHRC1/GPR180 信号转导整合到 TGFβ 信号转导中作为一个替代轴,以微调和实现该途径的低水平激活,以防止病理生理反应,同时有助于控制葡萄糖和能量代谢。