1. Phosphocholine accumulation and PHOSPHO1 depletion promote adipose tissue thermogenesis
- Author
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Tony E. Chavarria, Bingbing Yuan, Mengxi Jiang, Harvey F. Lodish, and Nai-Jia Huang
- Subjects
Phosphorylcholine ,Adipose tissue ,chemistry.chemical_compound ,Mice ,Insulin resistance ,Adipose Tissue, Brown ,Commentaries ,Brown adipose tissue ,Gene expression ,medicine ,Choline ,Animals ,Uncoupling Protein 1 ,Phosphocholine ,Mice, Knockout ,Multidisciplinary ,Thermogenesis ,Biological Sciences ,medicine.disease ,Phosphoric Monoester Hydrolases ,Cell biology ,Cold Temperature ,Mice, Inbred C57BL ,medicine.anatomical_structure ,Adipocytes, Brown ,chemistry ,Adipose Tissue ,Knockout mouse - Abstract
Phosphocholine phosphatase-1 (PHOSPHO1) is a phosphocholine phosphatase that catalyzes the hydrolysis of phosphocholine (PC) to choline. Here we demonstrate that the PHOSPHO1 transcript is highly enriched in mature brown adipose tissue (BAT) and is further induced by cold and isoproterenol treatments of BAT and primary brown adipocytes. In defining the functional relevance of PHOPSPHO1 in BAT thermogenesis and energy metabolism, we show that PHOSPHO1 knockout mice are cold-tolerant, with higher expression of thermogenic genes in BAT, and are protected from high-fat diet-induced obesity and development of insulin resistance. Treatment of mice with the PHOSPHO1 substrate phosphocholine is sufficient to induce cold tolerance, thermogenic gene expression, and allied metabolic benefits. Our results reveal a role of PHOSPHO1 as a negative regulator of BAT thermogenesis, and inhibition of PHOSPHO1 or enhancement of phosphocholine represent innovative approaches to manage the metabolic syndrome.
- Published
- 2020