胸腺基质淋巴细胞生成素
脂肪组织
间质细胞
免疫系统
白色脂肪组织
先天性淋巴细胞
内分泌学
细胞因子
免疫学
内科学
生物
医学
癌症研究
先天免疫系统
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,Brian Kim,John T. Seykora
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-07-29
卷期号:373 (6554)
被引量:78
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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