Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress

Thermogenic proteins are down-regulated under thermal stress, including PGC1α· However, the molecular mechanisms are not fully understood. Here, we addressed that chaperone-mediated autophagy could regulate the stability of PGC1α under thermal stress. In mice, knockdown of Lamp2a, one of the two components of CMA, in BAT showed increased PGC1α protein and improved metabolic phenotypes. Combining the proteomics of brown adipose tissue (BAT), structure prediction, co-immunoprecipitation- mass spectrum and biochemical assays, we found that PARK7, a Parkinson's disease causative protein, could sense the temperature changes and interact with LAMP2A and HSC70, respectively, subsequently manipulate the activity of CMA. Knockout of Park7 specific in BAT promoted BAT whitening, leading to impaired insulin sensitivity and energy expenditure at thermoneutrality. Moreover, inhibiting the activity of CMA by knockdown of LAMP2A reversed the effects induced by Park7 ablation. These findings suggest CMA is required for BAT to sustain thermoneutrality-induced whitening through degradation of PGC1α.

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Publication Details

Journal
Nature Communications
Published
2025-05-14
DOI
https://doi.org/10.1038/s41467-025-59618-0
Citations
4
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
5.42

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article

Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress

Yixiao Zhuang, Hanyin Zhang, Xingxing Kong, Peijie Chen et al.
4 citations
Nature Communications
Autophagy in Disease and Therapy
5.42
article

Chaperone-mediated autophagy manipulates PGC1α stability and governs energy metabolism under thermal stress

Yixiao Zhuang, Hanyin Zhang, Xingxing Kong, Peijie Chen, Yunpeng Sun, Peng Zou, Xiaodan Lü, Yonghao Feng, John Li, Shuang Zhang, Yuxuan Chen, Jin Li, Xinyi Zhang, H.S. Gao, Hui Wang, Yi Xu
article en
4 citations

Abstract

Thermogenic proteins are down-regulated under thermal stress, including PGC1α· However, the molecular mechanisms are not fully understood. Here, we addressed that chaperone-mediated autophagy could regulate the stability of PGC1α under thermal stress. In mice, knockdown of Lamp2a, one of the two components of CMA, in BAT showed increased PGC1α protein and improved metabolic phenotypes. Combining the proteomics of brown adipose tissue (BAT), structure prediction, co-immunoprecipitation- mass spectrum and biochemical assays, we found that PARK7, a Parkinson's disease causative protein, could sense the temperature changes and interact with LAMP2A and HSC70, respectively, subsequently manipulate the activity of CMA. Knockout of Park7 specific in BAT promoted BAT whitening, leading to impaired insulin sensitivity and energy expenditure at thermoneutrality. Moreover, inhibiting the activity of CMA by knockdown of LAMP2A reversed the effects induced by Park7 ablation. These findings suggest CMA is required for BAT to sustain thermoneutrality-induced whitening through degradation of PGC1α.

Nature CommunicationsVol. 16(1)
Shanghai University of Sport (CN), Chinese Academy of Sciences (CN), Fudan University (CN), People 's Hospital of Jilin Province (CN), Shanghai Institute of Organic Chemistry (CN), Huashan Hospital (CN), Nanjing Medical University (CN)
National Natural Science Foundation of China, Fudan University, State Key Laboratory of Genetic Engineering
Affordable and clean energy
Openalex Percentile: Top 4%
Autophagy in Disease and Therapy
5.42
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