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由HIV包膜糖蛋白诱导的未感染细胞的凋亡。

Apoptosis of uninfected cells induced by HIV envelope glycoproteins.

作者信息

Ahr Barbara, Robert-Hebmann Véronique, Devaux Christian, Biard-Piechaczyk Martine

机构信息

Laboratoire Infections Rétrovirales et Signalisation Cellulaire, CNRS UMR 5121-UM1, Institut de Biologie, 4, Bd Henri IV, CS 89508, 34960 Montpellier Cedex 2, France.

出版信息

Retrovirology. 2004 Jun 23;1:12. doi: 10.1186/1742-4690-1-12.

Abstract

Apoptosis, or programmed cell death, is a key event in biologic homeostasis but is also involved in the pathogenesis of many human diseases including human immunodeficiency virus (HIV) infection. Although multiple mechanisms contribute to the gradual T cell decline that occurs in HIV-infected patients, programmed cell death of uninfected bystander T lymphocytes, including CD4+ and CD8+ T cells, is an important event leading to immunodeficiency. The HIV envelope glycoproteins (Env) play a crucial role in transducing this apoptotic signal after binding to its receptors, the CD4 molecule and a coreceptor, essentially CCR5 and CXCR4. Depending on Env presentation, the receptor involved and the complexity of target cell contact, apoptosis induction is related to death receptor and/or mitochondria-dependent pathways. This review summarizes current knowledge of Env-mediated cell death leading to T cell depletion and clinical complications and covers the sometimes conflicting studies that address the possible mechanisms of T cell death.

摘要

细胞凋亡,即程序性细胞死亡,是生物体内稳态中的关键事件,但也参与包括人类免疫缺陷病毒(HIV)感染在内的许多人类疾病的发病机制。尽管多种机制导致了HIV感染患者体内T细胞的逐渐减少,但未感染的旁观者T淋巴细胞(包括CD4+和CD8+ T细胞)的程序性细胞死亡是导致免疫缺陷的重要事件。HIV包膜糖蛋白(Env)在与其受体(CD4分子和共受体,主要是CCR5和CXCR4)结合后,在转导这种凋亡信号中起关键作用。根据Env的呈现方式、所涉及的受体以及靶细胞接触的复杂性,凋亡诱导与死亡受体和/或线粒体依赖性途径有关。本综述总结了目前关于Env介导的导致T细胞耗竭和临床并发症的细胞死亡的知识,并涵盖了有时相互矛盾的关于T细胞死亡可能机制的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac95/446229/5e0ab9cbf372/1742-4690-1-12-1.jpg

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