Instituto de Biologia Molecular e Celular, University of Porto, Rua do Campo Alegre 823, Porto, Portugal.
J Leukoc Biol. 2010 Nov;88(5):885-96. doi: 10.1189/jlb.0410205. Epub 2010 Jun 21.
Triggering of phagocyte apoptosis is a major virulence mechanism used by some successful bacterial pathogens. A central issue in the apoptotic death context is that fully developed apoptosis results in necrotic cell autolysis (secondary necrosis) with release of harmful cell components. In multicellular animals, this occurs when apoptosing cells are not removed by scavengers, mainly macrophages. Secondary necrotic lysis of neutrophils and macrophages may occur in infection when extensive phagocyte apoptosis is induced by bacterial cytotoxins and removal of apoptosing phagocytes is defective because the apoptotic process exceeds the available scavenging capacity or targets macrophages directly. Induction of phagocyte secondary necrosis is an important pathogenic mechanism, as it combines the pathogen evasion from phagocyte antimicrobial activities and the release of highly cytotoxic molecules, particularly of neutrophil origin, such as neutrophil elastase. This pathogenicity mechanism therefore promotes the unrestricted multiplication of the pathogen and contributes directly to the pathology of several necrotizing infections, where extensive apoptosis and necrosis of macrophages and neutrophils are present. Here, examples of necrotizing infectious diseases, where phagocyte secondary necrosis is implicated, are reviewed.
吞噬细胞凋亡的触发是某些成功的细菌病原体使用的主要毒力机制。在凋亡死亡的情况下,一个核心问题是完全发育的凋亡导致坏死的细胞自溶(继发性坏死),释放有害的细胞成分。在多细胞动物中,当凋亡细胞没有被清道夫(主要是巨噬细胞)清除时,就会发生这种情况。当细菌细胞毒素诱导大量吞噬细胞凋亡,而清除凋亡吞噬细胞存在缺陷时,例如凋亡过程超过可用的清除能力或直接靶向巨噬细胞,中性粒细胞和巨噬细胞的继发性坏死性溶解可能会在感染中发生。吞噬细胞继发性坏死的诱导是一种重要的发病机制,因为它结合了病原体逃避吞噬细胞抗菌活性和释放高细胞毒性分子,特别是来自中性粒细胞的分子,如中性粒细胞弹性蛋白酶。因此,这种致病性机制促进了病原体的不受限制的繁殖,并直接导致几种坏死性感染的病理学,其中存在巨噬细胞和中性粒细胞的广泛凋亡和坏死。在这里,我们回顾了吞噬细胞继发性坏死与之相关的几种坏死性传染病的例子。