Hydrolysis of epithelial junctional proteins by Porphyromonas gingivalis gingipains

被引:117
作者
Katz, J
Yang, QB
Zhang, P
Potempa, J
Travis, J
Michalek, SM
Balkovetz, DF
机构
[1] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Oral Biol, Birmingham, AL 35294 USA
[3] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
[4] Univ Alabama, Dept Cell Biol, Birmingham, AL 35294 USA
[5] Vet Adm Med Ctr, Birmingham, AL 35233 USA
[6] Jagiellonian Univ, Inst Microbiol & Immunol, Krakow, Poland
[7] Univ Georgia, Dept Biochem & Mol Biol, Athens, GA 30602 USA
关键词
D O I
10.1128/IAI.70.5.2512-2518.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Porphyromonas gingivalis has been implicated as an etiologic agent of adult periodontitis. We have previously shown that P. gingivalis can degrade the epithelial cell-cell junction complexes, thus suggesting that this bacterium can invade the underlying connective tissues via a paracellular pathway. However, the precise mechanism(s) involved in this process has not been elucidated. The purpose of this study was to determine if the arginine- and lysine-specific gingipains of P. gingivalis (i.e., HRgpA and RgpB, and Kgp, respectively) were responsible for the degradation of E-cadherin, the cell-cell adhesion protein in the adherens junctions. In addition, we compared the degradative abilities of the whole gingipains HRgpA and Kgp to those of their catalytic domains alone. In these studies, immunoprecipitated E-cadherin as well as monolayers of polarized Madin-Darby canine kidney (MDCK) epithelial cell cultures were incubated with the gingipains and hydrolysis of E-cadherin was assessed by Western blot analysis. Incubation of P. gingivalis cells with immunoprecipitated E-cadherin resulted in degradation, whereas prior exposure of P. gingivalis cells to leupeptin and especially acetyl-Leu-Val-Lys-aldehyde (which are arginine- and lysine-specific inhibitors, respectively) reduced this activity. Furthermore, incubation of E-cadherin immunoprecipitates with the different gingipains resulted in an effective and similar hydrolysis of the protein. However, when monolayers of MDCK cells were exposed to the gingipains, Kgp was Most effective in hydrolyzing the E-cadherin molecules in the adherens junction. Kgp was more effective than its catalytic domain in degrading E-cadherin at 500 nM but not at a lower concentration (250 nM). These results suggest that the hemagglutinin domain of Kgp plays a role in degradation and that there is a critical threshold concentration for this activity. Taken together, these results provide evidence that the gingipains, especially Kgp, are involved in the degradation of the adherens junction of epithelial cells, which may be important in the invasion of periodontal connective tissue by P. gingivalis.
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页码:2512 / 2518
页数:7
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