Equipe Communication Intercellulaire et Infections Microbiennes, Centre de Recherche Interdisciplinaire en Biologie (CIRB), Collège de France, 11 Place Marcelin Berthelot, Paris 75005, France; Inserm, U1050, Paris 75005, France; Centre national de la Recherche Scientifique (CNRS), UMR7241, Paris 75005, France; MEMOLIFE Laboratory of excellence and Paris Sciences et Lettres, Paris 75005, France.
Unité de Chronobiologie Théorique, Université Libre de Bruxelles, CP231, Boulevard du Triomphe, 1050 Brussels, Belgium.
Biochim Biophys Acta Mol Cell Res. 2018 Nov;1865(11 Pt B):1838-1845. doi: 10.1016/j.bbamcr.2018.08.007. Epub 2018 Aug 18.
Recent reports have highlighted the pivotal role of Ca during host cell infection by bacterial pathogens. Here, we review how bacterial pore-forming toxins (PFTs) trigger global Ca signals to regulate cell adhesion-, inflammatory- or death processes. We comment recent reports describing the role of bacterial effectors injected by a type III secretion system (T3SS) as well as host cell players in the formation of Ca microdomains during Shigella invasion and Chlamydia extrusion of host cells. We discuss how modeling and comparison between bacterial-induced and physiological Ca microdomains provides insight into the critical parameters shaping the duration of local Ca responses.
最近的报告强调了 Ca 在细菌病原体感染宿主细胞过程中的关键作用。在这里,我们回顾了细菌孔形成毒素 (PFT) 如何引发全局 Ca 信号来调节细胞黏附、炎症或死亡过程。我们评论了最近的报告,描述了由 III 型分泌系统 (T3SS) 注入的细菌效应子以及宿主细胞在志贺氏菌入侵和衣原体挤出宿主细胞过程中形成 Ca 微区的作用。我们讨论了如何通过对细菌诱导的和生理 Ca 微区之间的建模和比较来深入了解塑造局部 Ca 反应持续时间的关键参数。