| Literature DB >> 34326208 |
Ruth Choa1, Junichiro Tohyama1, Shogo Wada2, Hu Meng3, Jian Hu4, Mariko Okumura1, Rebecca M May5, Tanner F Robertson1,6, Ruth-Anne Langan Pai1, Arben Nace7, Christian Hopkins7, Elizabeth A Jacobsen8, Malay Haldar1, Garret A FitzGerald3, Edward M Behrens9, Andy J Minn10, Patrick Seale11, George Cotsarelis7, Brian Kim12,13,14,15, John T Seykora7, Mingyao Li4, Zoltan Arany2, Taku Kambayashi16.
Abstract
Emerging studies indicate that the immune system can regulate systemic metabolism. Here, we show that thymic stromal lymphopoietin (TSLP) stimulates T cells to induce selective white adipose loss, which protects against obesity, improves glucose metabolism, and mitigates nonalcoholic steatohepatitis. Unexpectedly, adipose loss was not caused by alterations in food intake, absorption, or energy expenditure. Rather, it was induced by the excessive loss of lipids through the skin as sebum. TSLP and T cells regulated sebum release and sebum-associated antimicrobial peptide expression in the steady state. In human skin, TSLP expression correlated directly with sebum-associated gene expression. Thus, we establish a paradigm in which adipose loss can be achieved by means of sebum hypersecretion and uncover a role for adaptive immunity in skin barrier function through sebum secretion.Entities:
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Year: 2021 PMID: 34326208 PMCID: PMC8917823 DOI: 10.1126/science.abd2893
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728