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革兰氏阳性菌对细胞凋亡的调控:机制多样性及其对免疫的影响

Regulation of Apoptosis by Gram-Positive Bacteria: Mechanistic Diversity and Consequences for Immunity.

作者信息

Ulett Glen C, Adderson Elisabeth E

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.

出版信息

Curr Immunol Rev. 2006 May;2(2):119-141. doi: 10.2174/157339506776843033.

Abstract

Apoptosis, or programmed cell death (PCD), is an important physiological mechanism, through which the human immune system regulates homeostasis and responds to diverse forms of cellular damage. PCD may also be involved in immune counteraction to microbial infection. Over the past decade, the amount of research on bacteria-induced PCD has grown tremendously, and the implications of this mechanism on immunity are being elucidated. Some pathogenic bacteria actively trigger the suicide response in critical lineages of leukocytes that orchestrate both the innate and adaptive immune responses; other bacteria proactively prevent PCD to benefit their own survival and persistence. Currently, the microbial virulence factors, which represent the keys to unlocking the suicide response in host cells, are a primary focus of this field. In this review, we discuss these bacterial "apoptosis regulatory molecules" and the apoptotic events they either trigger or prevent, the host target cells of this regulatory activity, and the possible ramifications for immunity to infection. Gram-positive pathogens including Staphylococcus, Streptococcus, Bacillus, Listeria, and Clostridia species are discussed as important agents of human infection that modulate PCD pathways in eukaryotic cells.

摘要

细胞凋亡,即程序性细胞死亡(PCD),是一种重要的生理机制,人体免疫系统通过该机制调节体内平衡并应对各种形式的细胞损伤。PCD也可能参与对微生物感染的免疫反击。在过去十年中,关于细菌诱导的PCD的研究数量大幅增长,并且这种机制对免疫的影响正在得到阐明。一些病原菌会在协调固有免疫和适应性免疫反应的关键白细胞谱系中积极触发自杀反应;其他细菌则主动阻止PCD以利于自身的存活和持续存在。目前,作为开启宿主细胞自杀反应关键的微生物毒力因子是该领域的主要研究重点。在这篇综述中,我们讨论这些细菌“凋亡调节分子”以及它们所触发或阻止的凋亡事件、这种调节活性的宿主靶细胞,以及对感染免疫可能产生的影响。包括葡萄球菌、链球菌、芽孢杆菌、李斯特菌和梭菌属在内的革兰氏阳性病原体被作为调节真核细胞中PCD途径的重要人类感染病原体进行讨论。

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