CLCF1 inhibits energy expenditure via suppressing brown fat thermogenesis

Author:

Yuan Youwen123ORCID,Li Kangli4,Ye Xueru123,Wen Shiyi56ORCID,Zhang Yanan123,Teng Fei123,Zhou Xuan123,Deng Yajuan123,Yang Xiaoyu123,Wang Weiwei123,Lin Jiayang123ORCID,Luo Shenjian123,Zhang Peizhen123,Shi Guojun56ORCID,Zhang Huijie123ORCID

Affiliation:

1. Department of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China

2. Guangdong Provincial Key Laboratory of Shock and Microcirculation, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China

3. State Key Laboratory of Organ Failure Research, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China

4. Department of Endocrinology, Translational Research of Diabetes Key Laboratory of Chongqing Education Commission of China, The Second Affiliated Hospital of Army Medical University, Chongqing 400037, China

5. Department of Endocrinology and Metabolism, Medical Center for Comprehensive Weight Control, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China

6. Guangdong Provincial Key Laboratory of Diabetology & Guangzhou Municipal Key Laboratory of Mechanistic and Translational Obesity Research, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China

Abstract

Brown adipose tissue (BAT) is the main site of nonshivering thermogenesis which plays an important role in thermogenesis and energy metabolism. However, the regulatory factors that inhibit BAT activity remain largely unknown. Here, cardiotrophin-like cytokine factor 1 (CLCF1) is identified as a negative regulator of thermogenesis in BAT. Adenovirus-mediated overexpression of CLCF1 in BAT greatly impairs the thermogenic capacity of BAT and reduces the metabolic rate. Consistently, BAT-specific ablation of CLCF1 enhances the BAT function and energy expenditure under both thermoneutral and cold conditions. Mechanistically, adenylate cyclase 3 (ADCY3) is identified as a downstream target of CLCF1 to mediate its role in regulating thermogenesis. Furthermore, CLCF1 is identified to negatively regulate the PERK-ATF4 signaling axis to modulate the transcriptional activity of ADCY3, which activates the PKA substrate phosphorylation. Moreover, CLCF1 deletion in BAT protects the mice against diet-induced obesity by promoting BAT activation and further attenuating impaired glucose and lipid metabolism. Therefore, our results reveal the essential role of CLCF1 in regulating BAT thermogenesis and suggest that inhibiting CLCF1 signaling might be a potential therapeutic strategy for improving obesity-related metabolic disorders.

Funder

MOST | National Key Research and Development Program of China

MOST | National Natural Science Foundation of China

Joint Funds of the National Natural Science Foundation of China

Key-Area Clinical Research Program of Southern Medical University

GDSTC | Basic and Applied Basic Research Foundation of Guangdong Province

MOST | NSFC | National Science Fund for Distinguished Young Scholars

Guangzhou Science and Technology Plan Project

Publisher

Proceedings of the National Academy of Sciences

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