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Enhanced Microscopic Definition of Campylobacter jejuni 81-176 Adherence to Invasion of Translocation across and Exocytosis from Polarized Human Intestinal Caco-2 Cells

机译:空肠弯曲菌81-176的增强的微观定义对极化人肠道Caco-2细胞的粘附侵袭跨位转运和胞吐作用

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摘要

Campylobacter jejuni-mediated pathogenesis involves gut adherence and translocation across intestinal cells. The current study was undertaken to examine the C. jejuni interaction with and translocation across differentiated Caco-2 cells to better understand Campylobacter's pathogenesis. The efficiency of C. jejuni 81-176 invasion of Caco-2 cells was two- to threefold less than the efficiency of invasion of INT407 cells. Adherence-invasion analyses indicated that C. jejuni 81-176 adhered to most INT407 cells but invaded only about two-thirds of the host cells over 2 h (two bacteria/cell). In contrast, only 11 to 17% of differentiated Caco-2 cells were observed to bind and internalize either C. jejuni strain 81-176 or NCTC 11168, and a small percentage of infected Caco-2 cells contained 5 to 20 internalized bacteria per cell after 2 h. Electron microscopy revealed that individual C. jejuni cells adhered to the tips of host cell microvilli via intimate flagellar contacts and by lateral bacterial binding to the sides of microvilli. Next, bacteria were observed to bind at the apical host membrane surface via presumed interactions at one pole of the bacterium and with host membrane protrusions located near intercellular junctions. The latter contacts apparently resulted in coordinated, localized plasma membrane invagination, causing simultaneous internalization of bacteria into an endosome. Passage of this Campylobacter endosome intracellularly from the apical surface to the basolateral surface occurred over time, and bacterial release apparently resulted from endosome-basolateral membrane fusion (i.e., exocytosis). Bacteria were found intercellularly below tight junctions at 60 min postinfection, but not at earlier times. This study revealed unique host cell adherence contacts, early endocytosis-specific structures, and a presumptive exocytosis component of the transcellular transcytosis route.
机译:空肠弯曲杆菌介导的发病机制涉及肠道黏附和跨肠细胞转运。当前的研究是为了检查空肠弯曲杆菌与分化的Caco-2细胞之间的相互作用和跨移位,以更好地了解弯曲杆菌的发病机理。空肠弯曲杆菌81-176侵袭Caco-2细胞的效率比INT407细胞侵袭效率低2-3倍。粘附侵袭分析表明,空肠弯曲杆菌81-176粘附于大多数INT407细胞,但在2小时内仅侵袭了约三分之二的宿主细胞(每个细菌两个细菌)。相反,仅观察到11%至17%的分化的Caco-2细胞结合并内化空肠弯曲杆菌菌株81-176或NCTC 11168,并且一小部分受感染的Caco-2细胞每个细胞包含5至20个内在细菌2小时后。电镜显示单个空肠弯曲杆菌细胞通过紧密的鞭毛接触和侧向细菌结合到微绒毛的侧面而粘附在宿主细胞微绒毛的尖端。接下来,观察到细菌通过在细菌的一个极点上的推测相互作用和位于细胞间连接附近的宿主膜突起而结合在根宿主膜表面。后者的接触显然导致协调的局部质膜内陷,导致细菌同时内化为内体。随着时间的流逝,这种弯曲杆菌内体从顶表面到基底外侧表面从细胞内通过,并且细菌释放显然是由内体-基底外侧膜融合(即胞吐作用)引起的。在感染后60分钟发现细菌在紧密连接下方的细胞间,但在更早的时候没有发现。这项研究揭示了独特的宿主细胞粘附接触,早期的内吞作用特定结构以及跨细胞转胞吞途径的推测的胞吐作用成分。

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