Abstract
AbstractMetabolic dysfunction-associated steatohepatitis (MASH, previously termed non-alcoholic steatohepatitis (NASH)), is a major complication of obesity that promotes fatty liver disease. MASH is characterized by progressive tissue fibrosis and sterile liver inflammation that can lead to liver cirrhosis, cancer, and death. The molecular mechanisms of fibrosis in MASH and its systemic control remain poorly understood. Here, we identified the secreted-type pro-fibrotic protein, procollagen C-endopeptidase enhancer-1 (PCPE-1), as a brown adipose tissue (BAT)-derived adipokine that promotes liver fibrosis in a murine obesity-induced MASH model. BAT-specific or systemic PCPE-1 depletion in mice ameliorated liver fibrosis, whereas, PCPE-1 gain of function in BAT enhanced hepatic fibrosis. High-calorie diet-induced ER stress increased PCPE-1 production in BAT through the activation of IRE-1/JNK/c-Fos/c-Jun signaling. Circulating PCPE-1 levels are increased in the plasma of MASH patients, suggesting a therapeutic possibility. In sum, our results uncover PCPE-1 as a novel systemic control factor of liver fibrosis.
Funder
MEXT | Japan Science and Technology Agency
MEXT | Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development
National Cerebral and Cardiovascular Center
Daiichi Sankyo Company
Roche Holding | Chugai Pharmaceutical
Uehara Memorial Foundation
Kowa Life Science Foundation
Manpei Suzuki Diabetes Foundation
MSD Life Science Foundation, Public Interest Incorporated Foundation
Kanae Foundation for the Promotion of Medical Science
Inamori Foundation
Terumo Foundation for Life Sciences and Arts
SENSHIN Medical Research Foundation
Ono Medical Research Foundation
Heiwa Nakajima Foundation
Suzuken Memorial Foundation
Hokuto Foundation for Bioscience
Mochida Memorial Foundation for Medical and Pharmaceutical Research
Cell Science Research Foundation
Daiichi Sankyo Foundation of Life Science
Tokyo Biochemical Research Foundation
Astellas Foundation for Research on Metabolic Disorders
Naito Foundation
Japan Geriatrics Society
Japan Diabetes Foundation
Kobayashi Magobei Memorial Medical Promotion Foundation of Japan
President's Grant for Interfaculty Collaboration Juntendo University
Japanese Circulation Society Grant for Future-Pioneering Doctors for Basic Research
Life Science Foundation of Japan
grant from Bourbon
Japan Foundation for Applied Enzymology
Publisher
Springer Science and Business Media LLC
Reference60 articles.
1. Ali D, Figeac F, Caci A, Ditzel N, Schmal C, Kerckhofs G, Havelund J, Faergeman N, Rauch A, Tencerova M et al (2022a) Gene Expression Omnibus GSE194075. https://www.ncbinlmnihgov/geo/query/acccgi?acc=GSE194075 [DATASET]
2. Ali D, Figeac F, Caci A, Ditzel N, Schmal C, Kerckhofs G, Havelund J, Faergeman N, Rauch A, Tencerova M et al (2022b) High-fat diet-induced obesity augments the deleterious effects of estrogen deficiency on bone: Evidence from ovariectomized mice. Aging Cell 21:e13726
3. Almind K, Kahn CR (2004a) Gene Expression Omnibus 123394. https://www.ncbinlmnihgov/geo/query/acccgi?acc=GSE123394 [DATASET]
4. Almind K, Kahn CR (2004b) Genetic determinants of energy expenditure and insulin resistance in diet-induced obesity in mice. Diabetes 53:3274–3285
5. Bartelt A, Bruns OT, Reimer R, Hohenberg H, Ittrich H, Peldschus K, Kaul MG, Tromsdorf UI, Weller H, Waurisch C et al (2011) Brown adipose tissue activity controls triglyceride clearance. Nat Med 17:200–205