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结核分枝杆菌基因组中的 RD1 基因座通过提高细胞质钙水平和钙蛋白酶激活促进感染巨噬细胞中白细胞介素-1α的成熟和分泌。

The RD1 locus in the Mycobacterium tuberculosis genome contributes to the maturation and secretion of IL-1α from infected macrophages through the elevation of cytoplasmic calcium levels and calpain activation.

机构信息

Department of Pathogenic Biology and Immunology, School of Medicine, Southeast University, Nanjing, China; Department of Microbiology, Kyoto University Graduate School of Medicine, Sakyo-ku, Kyoto, Japan.

出版信息

Pathog Dis. 2014 Feb;70(1):51-60. doi: 10.1111/2049-632X.12075. Epub 2013 Aug 23.

Abstract

Region of difference 1 (RD1) is a genomic locus in the Mycobacterium tuberculosis genome that has been shown to participate in the virulence of the bacterium, induction of cell death, and cytokine secretion in infected macrophages. In this study, we investigated the role of RD1 in interleukin-1α (IL-1α) secretion. M. tuberculosis H37Rv strain, but not a mutant strain deficient for RD1 (∆RD1), significantly induced IL-1α secretion from infected macrophages. Although IL-1α secretion was only observed in H37Rv-infected macrophages, there was no difference in the level of IL-1α transcription and pro-IL1α synthesis after infection with H37Rv and ∆RD1. Interestingly, ∆RD1 infection did not increase intracellular Ca(2+) levels, and Ca(2+) chelators markedly inhibited IL-1α secretion in response to H37Rv infection. Moreover, the inability of ∆RD1 to induce IL-1α secretion was restored by treatment with the calcium ionophore A23187. A significant increase in calpain activity was detected in macrophages infected with H37Rv, but not with ∆RD1, and calpain inhibitors abrogated IL-1α secretion. Taken together, these results suggest that in M. tuberculosis-infected macrophages, RD1 contributed to maturation and secretion of IL-1α by enhancing the influx of Ca(2+) followed by calpain activation.

摘要

区域差异 1(RD1)是结核分枝杆菌基因组中的一个基因座,已被证明参与细菌的毒力、感染巨噬细胞的细胞死亡诱导和细胞因子分泌。在这项研究中,我们研究了 RD1 在白细胞介素-1α(IL-1α)分泌中的作用。结核分枝杆菌 H37Rv 株而非缺乏 RD1(∆RD1)的突变株显著诱导感染巨噬细胞中 IL-1α 的分泌。尽管仅在 H37Rv 感染的巨噬细胞中观察到 IL-1α 分泌,但在 H37Rv 和 ∆RD1 感染后,IL-1α 的转录水平和前体 IL1α 的合成没有差异。有趣的是,∆RD1 感染不会增加细胞内 Ca2+水平,并且 Ca2+螯合剂显著抑制了对 H37Rv 感染的 IL-1α 分泌。此外,用钙离子载体 A23187 处理可恢复 ∆RD1 诱导 IL-1α 分泌的能力。在感染 H37Rv 的巨噬细胞中检测到钙蛋白酶活性显著增加,但在感染 ∆RD1 的巨噬细胞中没有检测到,钙蛋白酶抑制剂阻断了 IL-1α 的分泌。总之,这些结果表明,在结核分枝杆菌感染的巨噬细胞中,RD1 通过增强钙内流并随后激活钙蛋白酶来促进 IL-1α 的成熟和分泌。

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