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共生细菌诱导炎症反应的蛋白酶放大作用:对足月和早产种族差异的影响。

Protease Amplification of the Inflammatory Response Induced by Commensal Bacteria: Implications for Racial Disparity in Term and Preterm Birth.

作者信息

Walsh Scott W, Nugent William H, Alam S M Khorshed, Washington Sonya L, Teves Maria, Jefferson Kimberly K, Strauss Jerome F

机构信息

Department of Obstetrics and Gynecology, School of Medicine, Virginia Commonwealth University, P.O. Box 980034, Richmond, VA, 23298-0034, USA.

Department of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, VA, 23298-0551, USA.

出版信息

Reprod Sci. 2020 Jan;27(1):246-259. doi: 10.1007/s43032-019-00011-w. Epub 2020 Jan 1.

Abstract

Decidual macrophages secrete proteases that activate protease-activated receptor 1 (PAR-1). We hypothesized that activation of the inflammatory response by bacteria is amplified by proteases, initiating labor. In addition, we hypothesized that commensal bacteria trigger an inflammatory response by activating NF-κB and TET methylcytosine dioxygenase 2 (TET2), a DNA de-methylase, via a protease amplified PAR-1, RhoA kinase (ROCK) pathway. To evaluate these hypotheses, we compared responses of mononuclear cells with Lactobacillus crispatus, prevalent in the vaginal microbiome of women of European ancestry, with L. iners and Fusobacterium nucleatum, which are more prevalent in vaginal samples collected from African-American women. Decidual tissue was collected at term not-in-labor (TNL), term labor (TL), spontaneous preterm labor (sPTL), and infected preterm labor (iPTL) and immunostained for PAR-1, TET2, and CD14. Mononuclear cells and THP-1 macrophage cells were treated with bacteria and elastase, a known activator of PAR-1. The inflammatory response was monitored by confocal microscopy of TET2 and the p65 subunit of NF-κB, as well as IL-8 production. Decidual staining for PAR-1, TET2, and CD14 increased TNL < TL < sPTL < iPTL. All treatments stimulated translocation of TET2 and p65 from the cytosol to the nucleus and increased IL-8, but L. iners and F. nucleatum caused more robust responses than L. crispatus. Inhibition of PAR-1 or ROCK prevented TET2 and p65 nuclear translocalization and increases in IL-8. Our findings demonstrate that proteases amplify the inflammatory response to commensal bacteria. The more robust response to bacteria prevalent in African-American women may contribute to racial disparities in preterm birth.

摘要

蜕膜巨噬细胞分泌激活蛋白酶激活受体1(PAR-1)的蛋白酶。我们推测,细菌激活的炎症反应会被蛋白酶放大,从而引发分娩。此外,我们推测共生细菌通过蛋白酶放大的PAR-1、RhoA激酶(ROCK)途径激活核因子κB(NF-κB)和DNA去甲基化酶TET甲基胞嘧啶双加氧酶2(TET2),从而引发炎症反应。为了验证这些假设,我们比较了单核细胞对卷曲乳杆菌(在欧洲血统女性的阴道微生物群中普遍存在)、惰性乳杆菌和具核梭杆菌(在非裔美国女性的阴道样本中更普遍)的反应。在足月未临产(TNL)、足月临产(TL)、自发性早产(sPTL)和感染性早产(iPTL)时收集蜕膜组织,并对PAR-1、TET2和CD14进行免疫染色。单核细胞和THP-1巨噬细胞用细菌和弹性蛋白酶(一种已知的PAR-1激活剂)处理。通过对TET2和NF-κB的p65亚基进行共聚焦显微镜观察以及监测白细胞介素-8(IL-8)的产生来监测炎症反应。PAR-1、TET2和CD14的蜕膜染色呈TNL < TL < sPTL < iPTL递增。所有处理均刺激TET2和p65从细胞质转位至细胞核,并增加IL-8,但惰性乳杆菌和具核梭杆菌比卷曲乳杆菌引起的反应更强烈。抑制PAR-1或ROCK可阻止TET2和p65的核转位以及IL-8的增加。我们的研究结果表明,蛋白酶会放大对共生细菌的炎症反应。对非裔美国女性中普遍存在的细菌的更强反应可能导致早产的种族差异。

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