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肠道微生物组的性别差异驱动激素依赖性自身免疫的调节。

Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity.

机构信息

Program in Genetics and Genome Biology, Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

出版信息

Science. 2013 Mar 1;339(6123):1084-8. doi: 10.1126/science.1233521. Epub 2013 Jan 17.

Abstract

Microbial exposures and sex hormones exert potent effects on autoimmune diseases, many of which are more prevalent in women. We demonstrate that early-life microbial exposures determine sex hormone levels and modify progression to autoimmunity in the nonobese diabetic (NOD) mouse model of type 1 diabetes (T1D). Colonization by commensal microbes elevated serum testosterone and protected NOD males from T1D. Transfer of gut microbiota from adult males to immature females altered the recipient's microbiota, resulting in elevated testosterone and metabolomic changes, reduced islet inflammation and autoantibody production, and robust T1D protection. These effects were dependent on androgen receptor activity. Thus, the commensal microbial community alters sex hormone levels and regulates autoimmune disease fate in individuals with high genetic risk.

摘要

微生物暴露和性激素对自身免疫性疾病有强大的影响,其中许多疾病在女性中更为常见。我们证明,生命早期的微生物暴露决定了性激素水平,并改变了非肥胖型糖尿病(NOD)小鼠 1 型糖尿病(T1D)模型的自身免疫进展。共生微生物的定植提高了血清睾丸酮水平,并保护 NOD 雄性免于 T1D。将成年雄性的肠道微生物群转移到未成熟的雌性中,改变了受体的微生物群,导致睾丸酮升高和代谢组学变化,胰岛炎症和自身抗体产生减少,以及 T1D 得到有效保护。这些影响依赖于雄激素受体的活性。因此,共生微生物群落改变了性激素水平,并调节了具有高遗传风险个体的自身免疫性疾病的命运。

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