Univ. Bourgogne Franche-Comté, Agrosup Dijon, Dijon France.
UMR 8253, Université de ParisInstitut Necker Enfants-Malades (INEM), INSERM U1151-CNRS, Paris, France.
Autophagy. 2022 Nov;18(11):2761-2762. doi: 10.1080/15548627.2022.2065437. Epub 2022 Apr 20.
Candida albicans (C. albicans) is an opportunistic pathogen causing infections ranging from superficial to life-threatening dissemination, in which C. albicans is able to translocate through the gut barrier into deeper organs. In its filamentous form (hyphae), C. albicans can invade epithelial cells by two mechanisms: epithelial cell-driven endocytosis and C. albicans-driven active penetration of host cell plasma membrane (PM). Autophagic machinery is known to be involved in the epithelial barrier maintenance, especially the intestinal barrier that is continuously challenged by exposure to the gut microbiota or to xenobiotics. The protective role of autophagy during C. albicans infection has been investigated in myeloid cells, however, far less was known regarding its role during infection of epithelial cells. Here, we demonstrated that key proteins of the autophagic machinery and vesicles presenting features of autophagosomes are recruited at C. albicans invasion sites. These events are associated with host PM damage caused by the active penetration of C. albicans. We showed that ATG5 and ATG16L1 proteins contribute to PM repair mediated by lysosomal membrane exocytosis and participate in protection of epithelial cells' integrity against C. albicans-induced cell death. Our findings extend the knowledge on emerging roles of the autophagic machinery in stress-related membrane dynamics.
白色念珠菌(Candida albicans,C. albicans)是一种机会致病菌,可引起从浅表到危及生命的播散性感染,在此过程中,C. albicans 能够通过肠道屏障转移到更深的器官。在其丝状形式(菌丝)中,C. albicans 可以通过两种机制侵袭上皮细胞:上皮细胞驱动的内吞作用和 C. albicans 驱动的宿主细胞质膜(PM)的主动穿透。已知自噬机制参与上皮屏障的维持,特别是肠道屏障,它不断受到肠道微生物群或外源性物质的挑战。自噬在白色念珠菌感染中的保护作用已在髓样细胞中进行了研究,然而,对于其在感染上皮细胞过程中的作用知之甚少。在这里,我们证明了自噬机制的关键蛋白和具有自噬体特征的囊泡在 C. albicans 入侵部位被招募。这些事件与 C. albicans 主动穿透引起的宿主 PM 损伤有关。我们表明 ATG5 和 ATG16L1 蛋白有助于溶酶体膜胞吐介导的 PM 修复,并参与保护上皮细胞的完整性免受 C. albicans 诱导的细胞死亡。我们的发现扩展了自噬机制在应激相关膜动力学中的新兴作用的知识。