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鉴定上皮细胞的3-磷酸甘油醛脱氢酶为与牙龈卟啉单胞菌菌毛结合的第二种分子。

Identification of glyceraldehyde-3-phosphate dehydrogenase of epithelial cells as a second molecule that binds to Porphyromonas gingivalis fimbriae.

作者信息

Sojar Hakimuddin T, Genco Robert J

机构信息

Department of Oral Biology, School of Dental Medicine, State University of New York at Buffalo, 213 Foster Hall, 3435 Main Street, Buffalo, NY 14214-3092, USA.

出版信息

FEMS Immunol Med Microbiol. 2005 Jul 1;45(1):25-30. doi: 10.1016/j.femsim.2005.01.006. Epub 2005 Feb 5.

Abstract

Binding of Porphyromonas gingivalis to the host cells is an essential step in the pathogenesis of periodontal disease. P. gingivalis binds to and invades epithelial cells, and fimbriae are thought to be involved in this process. In our earlier studies, two major epithelial cell components of 40 and 50 kDa were identified as potential fimbrial receptors. Sequencing of a cyanogen bromide digestion fragment of the 50-kDa component resulted in an internal sequence identical to keratin I molecules, and hence this cytokeratin represents one of the epithelial cell receptors for P. gingivalis fimbriae. In this study, the 40-kDa component of KB cells was isolated and its amino-terminal sequence determined. The N-terminal amino sequence was found to be GKVKVGVNGF and showed perfect homology with human glyceraldehyde-3-phosphate dehydrogenase (GAPDH). Furthermore, purified P. gingivalis fimbriae were found to bind to rabbit muscle GAPDH. Antibodies directed against internal peptide 49-68 and 69-90 of fimbrillin were shown to inhibit the binding of P. gingivalis and of fimbriae to epithelial cells. Antibodies against these peptides also inhibited the binding of fimbriae to GAPDH. Our results confirmed that the amino-terminal domain corresponding to amino residues 49-68 of the fimbrillin protein is the major GAPDH binding domain. These studies point to GAPDH as a major receptor for P. gingivalis major fimbriae and, as such, GAPDH likely plays a role in P. gingivalis adherence and colonization of the oral cavity, as well as triggering host cell processes involved in the pathogenesis of P. gingivalis infections.

摘要

牙龈卟啉单胞菌与宿主细胞的结合是牙周病发病机制中的关键步骤。牙龈卟啉单胞菌可与上皮细胞结合并侵入其中,菌毛被认为参与了这一过程。在我们早期的研究中,已鉴定出40 kDa和50 kDa的两种主要上皮细胞成分是潜在的菌毛受体。对50 kDa成分的溴化氰消化片段进行测序,得到了一段与角蛋白I分子相同的内部序列,因此这种细胞角蛋白代表了牙龈卟啉单胞菌菌毛的上皮细胞受体之一。在本研究中,分离出了KB细胞的40 kDa成分并测定了其氨基末端序列。发现其N端氨基酸序列为GKVKVGVNGF,与人类甘油醛-3-磷酸脱氢酶(GAPDH)具有完全同源性。此外,还发现纯化的牙龈卟啉单胞菌菌毛可与兔肌肉GAPDH结合。针对菌毛蛋白内部肽段49 - 68和69 - 90的抗体可抑制牙龈卟啉单胞菌及其菌毛与上皮细胞的结合。针对这些肽段的抗体也可抑制菌毛与GAPDH的结合。我们的结果证实,菌毛蛋白中对应于氨基酸残基49 - 68的氨基末端结构域是主要的GAPDH结合结构域。这些研究表明GAPDH是牙龈卟啉单胞菌主要菌毛的主要受体,因此,GAPDH可能在牙龈卟啉单胞菌在口腔中的黏附和定植中发挥作用,以及触发与牙龈卟啉单胞菌感染发病机制相关的宿主细胞过程。

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