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首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >Release of Helicobacter pylori vacuolating cytotoxin by both a specific secretion pathway and budding of outer membrane vesicles. Uptake of released toxin and vesicles by gastric epithelium.
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Release of Helicobacter pylori vacuolating cytotoxin by both a specific secretion pathway and budding of outer membrane vesicles. Uptake of released toxin and vesicles by gastric epithelium.

机译:通过特异性分泌途径和外膜囊泡出芽释放幽门螺杆菌空泡化细胞毒素。胃上皮吸收释放的毒素和囊泡。

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摘要

The mechanisms by which Helicobacter pylori releases its virulence factors are poorly known. Active secretion has been proposed for some products, including a vacuolating toxin (VacA). Outer membrane vesicles represent another mechanism by which some Gram-negative bacteria may release virulence factors. This study sought to localize VacA by immunocytochemistry in H. pylori cells, to determine whether H. pylori produces outer membrane vesicles, and to investigate whether such vesicles might constitute a vehicle for the delivery of bacterial virulence factors to the gastric mucosa. Small (50-300 nm) membrane vesicles were found in H. pylori culture media from both H. pylori strain 60190 and strain CCUG 17874. These vesicles appeared to originate from blebs arising on the bacterial outer membrane. VacA was immunolocalized in the periplasm and outer membrane of intact bacteria and also in outer membrane blebs and vesicles. Both soluble secreted VacA and VacA-containing vesicles bound to, and were internalized by, MKN28 cells and were detectable in the gastric mucosa from H. pylori-infected humans. The release of outer membrane vesicles by H. pylori may represent a mechanism, additional to secretory pathways, for the delivery of bacterial toxins and antigens to the gastric mucosa. Copyright 1999 John Wiley & Sons, Ltd.
机译:幽门螺杆菌释放其毒力因子的机制尚不清楚。对于某些产品,包括空泡毒素(VacA),已经提出主动分泌。外膜囊泡代表另一种机制,某些革兰氏阴性细菌可通过该机制释放毒力因子。这项研究试图通过免疫细胞化学在幽门螺杆菌细胞中定位VacA,以确定幽门螺杆菌是否产生外膜囊泡,并调查这种囊泡是否可能构成将细菌毒力因子输送至胃粘膜的媒介。在幽门螺杆菌培养基中发现了来自幽门螺杆菌菌株60190和CCUG 17874的小的(50-300 nm)膜囊泡。这些囊泡似乎起源于细菌外膜上产生的气泡。 VacA免疫定位在完整细菌的周质和外膜以及外膜小泡和囊泡中。可溶性分泌的VacA和含VacA的囊泡均与MKN28细胞结合并被MKN28细胞内在化,并且可在幽门螺杆菌感染的人的胃粘膜中检测到。幽门螺杆菌释放外膜囊泡可能是分泌途径之外的一种将细菌毒素和抗原输送到胃粘膜的机制。版权所有1999 John Wiley&Sons,Ltd.

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