Adipocyte lipin 1 expression associates with human metabolic health and regulates systemic metabolism in mice

脂肪细胞 新陈代谢 内分泌学 生物 内科学 细胞生物学 表达式(计算机科学) 医学 脂肪组织 计算机科学 程序设计语言
作者
Andrew LaPoint,Jason Singer,Daniel Ferguson,Trevor M. Shew,M. Katie Renkemeyer,Hector H. Palacios,Rachael L. Field,Sireeesha Yerrathota,Roshan Kumari,Mahalakshmi Shankaran,Gordon I. Smith,Jun Yoshino,Mai He,Gary J. Patti,Marc K. Hellerstein,Samuel Klein,E. Matthew Morris,Jonathan R. Brestoff,Brian N. Finck,Andrew J. Lutkewitte
出处
期刊:Journal of Clinical Investigation [American Society for Clinical Investigation]
标识
DOI:10.1172/jci169722
摘要

Dysfunctional adipose tissue is believed to promote the development of hepatic steatosis and systemic insulin resistance, but many of the mechanisms involved are still unclear. Lipin 1 catalyzes the conversion of phosphatidic acid to diacylglycerol (DAG), the penultimate step of triglyceride synthesis, which is essential for lipid storage. Herein we found that adipose tissue LPIN1 expression is decreased in people with obesity compared to lean subjects, and low LPIN1 expression correlated with multi-tissue insulin resistance and increased rates of hepatic de novo lipogenesis. Comprehensive metabolic and multi-omic phenotyping demonstrated that adipocyte-specific Lpin1-/- mice had a metabolically-unhealthy phenotype, including liver and skeletal muscle insulin resistance, hepatic steatosis, increased hepatic de novo lipogenesis, and transcriptomic signatures of metabolically associated steatohepatitis that was exacerbated by high-fat diets. We conclude that adipocyte lipin 1-mediated lipid storage is vital for preserving adipose tissue and systemic metabolic health, and its loss predisposes mice to metabolically associated steatohepatitis.
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