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肠道微生物组调节心理应激引起的炎症。

The Gut Microbiome Regulates Psychological-Stress-Induced Inflammation.

机构信息

The Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

The Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Immunity. 2020 Aug 18;53(2):417-428.e4. doi: 10.1016/j.immuni.2020.06.025. Epub 2020 Jul 30.

Abstract

Psychological stress has adverse effects on various human diseases, including those of the cardiovascular system. However, the mechanisms by which stress influences disease activity remain unclear. Here, using vaso-occlusive episodes (VOEs) of sickle cell disease as a vascular disease model, we show that stress promotes VOEs by eliciting a glucocorticoid hormonal response that augments gut permeability, leading to microbiota-dependent interleukin-17A (IL-17A) secretion from T helper 17 (Th17) cells of the lamina propria, followed by the expansion of the circulating pool of aged neutrophils that trigger VOEs. We identify segmented filamentous bacteria as the commensal essential for the stress-induced expansion of aged neutrophils that enhance VOEs in mice. Importantly, the inhibition of glucocorticoids synthesis, blockade of IL-17A, or depletion of the Th17 cell-inducing gut microbiota markedly reduces stress-induced VOEs. These results offer potential therapeutic targets to limit the impact of psychological stress on acute vascular occlusion.

摘要

心理压力对包括心血管系统疾病在内的各种人类疾病都有不良影响。然而,压力影响疾病活动的机制尚不清楚。在这里,我们使用镰状细胞病的血管阻塞发作(VOEs)作为血管疾病模型,表明压力通过引发糖皮质激素激素反应来促进 VOEs,从而增加肠道通透性,导致固有层中的 Th17 细胞依赖于微生物组的白细胞介素-17A(IL-17A)分泌,随后循环池中的衰老中性粒细胞扩张,引发 VOEs。我们确定了分段丝状细菌是共生的必要条件,可促进压力诱导的衰老中性粒细胞扩张,从而增强小鼠的 VOEs。重要的是,抑制糖皮质激素合成、阻断 IL-17A 或耗尽诱导 Th17 细胞的肠道微生物群可显著减少应激引起的 VOEs。这些结果为限制心理压力对急性血管闭塞的影响提供了潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a82/7461158/7a7cae3263a3/nihms-1616968-f0002.jpg

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