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TNFAIP8蛋白在调节细胞凋亡和李斯特菌感染中的关键作用。

Crucial roles of TNFAIP8 protein in regulating apoptosis and Listeria infection.

作者信息

Porturas Thomas P, Sun Honghong, Buchlis George, Lou Yunwei, Liang Xiaohong, Cathopoulis Terry, Fayngerts Svetlana, Johnson Derek S, Wang Zhaojun, Chen Youhai H

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104; and.

Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104; and Department of Immunology, Shandong University School of Medicine, Ji'nan 250012, People's Republic of China.

出版信息

J Immunol. 2015 Jun 15;194(12):5743-50. doi: 10.4049/jimmunol.1401987. Epub 2015 May 6.

Abstract

TNF-α-induced protein 8 (TNFAIP8 or TIPE) is a newly described regulator of cancer and infection. However, its precise roles and mechanisms of actions are not well understood. We report in this article that TNFAIP8 regulates Listeria monocytogenes infection by controlling pathogen invasion and host cell apoptosis in a RAC1 GTPase-dependent manner. TNFAIP8-knockout mice were resistant to lethal L. monocytogenes infection and had reduced bacterial load in the liver and spleen. TNFAIP8 knockdown in murine liver HEPA1-6 cells increased apoptosis, reduced bacterial invasion into cells, and resulted in dysregulated RAC1 activation. TNFAIP8 could translocate to plasma membrane and preferentially associate with activated RAC1-GTP. The combined effect of reduced bacterial invasion and increased sensitivity to TNF-α-induced clearance likely protected the TNFAIP8-knockout mice from lethal listeriosis. Thus, by controlling bacterial invasion and the death of infected cells through RAC1, TNFAIP8 regulates the pathogenesis of L. monocytogenes infection.

摘要

肿瘤坏死因子-α诱导蛋白8(TNFAIP8或TIPE)是一种新发现的癌症和感染调节因子。然而,其确切作用和作用机制尚未完全明确。我们在本文中报道,TNFAIP8通过以RAC1 GTP酶依赖性方式控制病原体入侵和宿主细胞凋亡来调节单核细胞增生李斯特菌感染。TNFAIP8基因敲除小鼠对致死性单核细胞增生李斯特菌感染具有抗性,且肝脏和脾脏中的细菌载量降低。在小鼠肝脏HEPA1-6细胞中敲低TNFAIP8可增加细胞凋亡、减少细菌侵入细胞,并导致RAC1激活失调。TNFAIP8可转运至质膜并优先与活化的RAC1-GTP结合。细菌入侵减少和对肿瘤坏死因子-α诱导的清除敏感性增加的综合作用可能保护TNFAIP8基因敲除小鼠免受致死性李斯特菌病的侵害。因此,通过RAC1控制细菌入侵和感染细胞的死亡,TNFAIP8调节单核细胞增生李斯特菌感染的发病机制。

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