微生物组作为内分泌干扰物的靶标:新的化学物质可能会破坏雄激素和微生物组介导的自身免疫

M. Baker
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引用次数: 1

摘要

在非肥胖型糖尿病(NOD)小鼠中,女性1型糖尿病发病率的增加存在性别偏倚。最近,人们发现这种微生物群可以保护雄性小鼠免受1型糖尿病的侵害。将微生物群从成年NOD雄性小鼠转移到青春期前雌性小鼠可防止性别偏倚型1型糖尿病的发生。这种保护部分涉及微生物组介导的睾酮合成增加,从而上调白细胞介素和干扰素途径。介导这种反应的微生物组衍生信号尚不清楚,尽管由于微生物组中合成的化学物质的多样性,有些可能具有与雄激素不同的结构。这表明新的合成和/或植物衍生的化学物质可能通过破坏微生物组与其宿主之间的保护性信号网络来影响性别偏倚的自身免疫性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The microbiome as a target for endocrine disruptors: Novel chemicals may disrupt androgen and microbiome-mediated autoimmunity
In non-obese diabetic (NOD) mice, there is a sex-biased increase in female incidence of type 1 diabetes. Recently, the microbiome was found to protect male mice from type 1 diabetes. Transfer of microbiota from adult NOD male mice to pre-pubertal female mice protects against later incidence of sex-biased type 1 diabetes. This protection involves, in part, microbiome-mediated increased testosterone synthesis, which up-regulates the interleukin and interferon pathways. The microbiome-derived signals that mediate this response are unknown, although due to the diversity of chemicals synthesized in the microbiome some are likely to have structures unlike androgens. This suggests that novel synthetic and/or plant-derived chemicals may affect sex-biased autoimmune diseases through disruption of protective signaling networks between the microbiome and its host.
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