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CD66受体不同的Opa特异性影响组织相互作用以及细胞对淋病奈瑟菌的反应。

Differential Opa specificities for CD66 receptors influence tissue interactions and cellular response to Neisseria gonorrhoeae.

作者信息

Gray-Owen S D, Lorenzen D R, Haude A, Meyer T F, Dehio C

机构信息

Max-Planck-Institut für Biologie, Abteilung Infektionsbiologie, Tübingen, Germany.

出版信息

Mol Microbiol. 1997 Dec;26(5):971-80. doi: 10.1046/j.1365-2958.1997.6342006.x.

Abstract

The ability of all 11 variable opacity (Opa) proteins encoded by Neisseria gonorrhoeae MS11 to interact directly with the five CD66 antigens was determined. Transfected HeLa cell lines expressing individual CD66 antigens were infected with recombinant N. gonorrhoeae and Escherichia coli strains expressing defined Opas. Based upon the ability of these bacteria to bind and invade and to isolate specifically CD66 antigens from detergent-soluble extracts of the corresponding cell lines, distinct specificity groups of Opa interaction with CD66 were seen. Defining these specificity groups allowed us to assign a specific function for CD66a in the Opa-mediated interaction of gonococci with two different target cell types, which are both known to co-express multiple CD66 antigens. The competence of individual Opas to interact with CD66a was strictly correlated with their ability to induce an oxidative response by polymorphonuclear neutrophils. The same Opa specificity was observed for the level of gonococcal binding to primary endothelial cells after stimulation with TNFalpha, which was shown to increase the expression of CD66a rather than CD66e. As CD66e alone is expressed on other target tissues of gonococcal pathogenicity, Opa variation probably contributes to the cell tropism displayed by gonococci.

摘要

测定了淋病奈瑟菌MS11编码的所有11种可变透明度(Opa)蛋白与5种CD66抗原直接相互作用的能力。用表达特定Opa的重组淋病奈瑟菌和大肠杆菌菌株感染表达单个CD66抗原的转染HeLa细胞系。基于这些细菌结合、侵袭以及从相应细胞系的去污剂可溶提取物中特异性分离CD66抗原的能力,观察到了Opa与CD66相互作用的不同特异性组。确定这些特异性组使我们能够为CD66a在淋球菌与两种不同靶细胞类型的Opa介导相互作用中指定特定功能,这两种靶细胞类型均已知共表达多种CD66抗原。单个Opa与CD66a相互作用的能力与其诱导多形核中性粒细胞氧化反应的能力严格相关。在用TNFα刺激后,观察到淋球菌与原代内皮细胞结合水平的Opa特异性相同,TNFα被证明可增加CD66a而非CD66e的表达。由于单独的CD66e在淋球菌致病性的其他靶组织上表达,Opa变异可能有助于淋球菌表现出的细胞嗜性。

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