| Literature DB >> 31341090 |
John Eom1, Jeong Jin Kim1, Seul Gi Yoon2, Haengdueng Jeong1, Soojin Son2, Jae Bong Lee1, Jihye Yoo1, Hyun Ju Seo2, Yejin Cho1, Ku Sul Kim1, Kyung Mi Choi1, Il Yong Kim2, Hui-Young Lee3,4, Ki Taek Nam1, Peter Cresswell5, Je Kyung Seong6,7,8, Jun-Young Seo9.
Abstract
Viperin is an interferon (IFN)-inducible multifunctional protein. Recent evidence from high-throughput analyses indicates that most IFN-inducible proteins, including viperin, are intrinsically expressed in specific tissues; however, the respective intrinsic functions are unknown. Here we show that the intrinsic expression of viperin regulates adipose tissue thermogenesis, which is known to counter metabolic disease and contribute to the febrile response to pathogen invasion. Viperin knockout mice exhibit increased heat production, resulting in a reduction of fat mass, improvement of high-fat diet (HFD)-induced glucose tolerance, and enhancement of cold tolerance. These thermogenic phenotypes are attributed to an adipocyte-autonomous mechanism that regulates fatty acid β-oxidation. Under an HFD, viperin expression is increased, and its function is enhanced. Our findings reveal the intrinsic function of viperin as a novel mechanism regulating thermogenesis in adipose tissues, suggesting that viperin represents a molecular target for thermoregulation in clinical contexts.Entities:
Keywords: fatty acid β-oxidation; innate immunity; metabolism; thermogenesis; viperin
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Year: 2019 PMID: 31341090 PMCID: PMC6717265 DOI: 10.1073/pnas.1904480116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205