胸腺基质淋巴细胞生成素
脂肪组织
间质细胞
内分泌学
炎症
化学
内科学
生物
医学
作者
Ruth Choa,Junichiro Tohyama,Shogo Wada,Hu Meng,Jian Hu,Mariko Okumura,Rebecca M. May,Tanner F. Robertson,Ruth-Anne Langan Pai,Arben Nace,Christian Hopkins,Elizabeth A. Jacobsen,Malay Haldar,Garret A. FitzGerald,Edward M. Behrens,Andy J. Minn,Patrick Seale,George Cotsarelis,B. Kim,John T. Seykora,Mingyao Li,Zoltan Arany,Taku Kambayashi
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-07-30
卷期号:373 (6554)
被引量:13
标识
DOI:10.1126/science.abd2893
摘要
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.
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