首页> 外文OA文献 >Porphyromonas gingivalis RgpA-Kgp Proteinase-Adhesin Complexes Penetrate Gingival Tissue and Induce Proinflammatory Cytokines or Apoptosis in a Concentration-Dependent Manner▿
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Porphyromonas gingivalis RgpA-Kgp Proteinase-Adhesin Complexes Penetrate Gingival Tissue and Induce Proinflammatory Cytokines or Apoptosis in a Concentration-Dependent Manner▿

机译:牙龈卟啉单胞菌RgpA-Kgp蛋白酶-粘附素复合物穿透牙龈组织并以浓度依赖的方式诱导促炎性细胞因子或凋亡opt

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摘要

The RgpA-Kgp proteinase-adhesin complexes of Porphyromonas gingivalis were observed, using immunostaining, in human gingival tissue associated with periodontitis but not in healthy tissue. The staining pattern suggested a concentration gradient from the subgingival plaque into the subjacent gingival connective tissue. Intense immunostaining was observed in areas displaying gross disturbance of tissue architecture. P. gingivalis cells and the RgpA-Kgp complexes at low concentrations were shown to stimulate secretory intercellular adhesion molecule 1, interleukin-8 (IL-8), IL-6, and macrophage chemoattractant protein secretion from cultured human epithelial (KB) and fibroblast (MRC-5) cells. However, at high concentrations a reduction in the level of these mediators was observed. In contrast, macrophage inflammatory protein 1α and IL-1α were stimulated only at high P. gingivalis cell concentrations. P. gingivalis cells and the RgpA-Kgp complexes were shown to induce apoptosis in KB and MRC-5 cells in a time- and dose-dependent manner. These data suggest that the RgpA-Kgp complexes penetrate the gingival connective tissue; at low concentrations distal from the plaque the complexes stimulate the secretion of proinflammatory mediators, while at high concentrations proximal to the plaque they induce apoptosis and attenuate the secretion of proinflammatory mediators.
机译:使用免疫染色在与牙周炎有关的人牙龈组织中观察到牙龈卟啉单胞菌的RgpA-Kgp蛋白酶-粘附素复合物,但在健康组织中未观察到。染色模式提示从龈下斑块到龈下结缔组织的浓度梯度。在显示出严重组织结构紊乱的区域观察到强烈的免疫染色。低浓度的牙龈卟啉单胞菌细胞和RgpA-Kgp复合物可刺激培养的人上皮细胞(KB)和成纤维细胞分泌分泌的细胞间粘附分子1,白细胞介素8(IL-8),IL-6和巨噬细胞趋化蛋白。 (MRC-5)细胞。然而,在高浓度下,观察到这些介体水平的降低。相反,仅在高牙龈卟啉单胞菌细胞浓度下刺激巨噬细胞炎性蛋白1α和IL-1α。已显示牙龈卟啉单胞菌细胞和RgpA-Kgp复合物以时间和剂量依赖性方式诱导KB和MRC-5细胞凋亡。这些数据表明,RgpA-Kgp复合物穿透了牙龈结缔组织。在菌斑远端低浓度下,复合物刺激促炎介质的分泌,而在菌斑近端高浓度下,复合物诱导细胞凋亡并减弱促炎介质的分泌。

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