首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Odontogenic Ameloblast-associated Protein (ODAM) Mediates Junctional Epithelium Attachment to Teeth via Integrin-ODAM-Rho Guanine Nucleotide Exchange Factor 5 (ARHGEF5)-RhoA Signaling
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Odontogenic Ameloblast-associated Protein (ODAM) Mediates Junctional Epithelium Attachment to Teeth via Integrin-ODAM-Rho Guanine Nucleotide Exchange Factor 5 (ARHGEF5)-RhoA Signaling

机译:牙源性成釉细胞相关蛋白(ODAM)通过整合素-ODAM-Rho鸟嘌呤核苷酸交换因子5(ARHGEF5)-RhoA信号介导结节上皮附着在牙齿上。

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摘要

Adhesion of the junctional epithelium (JE) to the tooth surface is crucial for maintaining periodontal health. Although odontogenic ameloblast-associated protein (ODAM) is expressed in the JE, its molecular functions remain unknown. We investigated ODAM function during JE development and regeneration and its functional significance in the initiation and progression of periodontitis and peri-implantitis. ODAM was expressed in the normal JE of healthy teeth but absent in the pathologic pocket epithelium of diseased periodontium. In periodontitis and peri-implantitis, ODAM was extruded from the JE following onset with JE attachment loss and detected in gingival crevicular fluid. ODAM induced RhoA activity and the expression of downstream factors, including ROCK (Rho-associated kinase), by interacting with Rho guanine nucleotide exchange factor 5 (ARHGEF5). ODAM-mediated RhoA signaling resulted in actin filament rearrangement. Reduced ODAM and RhoA expression in integrin β3- and β6-knockout mice revealed that cytoskeleton reorganization in the JE occurred via integrin-ODAM-ARHGEF5-RhoA signaling. Fibronectin and laminin activated RhoA signaling via the integrin-ODAM pathway. Finally, ODAM was re-expressed with RhoA in regenerating JE after gingivectomy in vivo. These results suggest that ODAM expression in the JE reflects a healthy periodontium and that JE adhesion to the tooth surface is regulated via fibronectin/laminin-integrin-ODAM-ARHGEF5-RhoA signaling. We also propose that ODAM could be used as a biomarker of periodontitis and peri-implantitis.
机译:连接上皮(JE)与牙齿表面的粘附对于维持牙周健康至关重要。尽管牙源性成釉细胞相关蛋白(ODAM)在JE中表达,但其分子功能仍然未知。我们调查了乙脑开发和再生期间的ODAM功能及其在牙周炎和种植体周围炎的发生和发展中的功能意义。 ODAM在健康牙齿的正常JE中表达,但在患牙周膜的病理性口袋上皮中不存在。在牙周炎和种植体周围炎中,ODAM发作后因JE附着丧失而从JE中挤出,并在龈沟液中检测到。 ODAM通过与Rho鸟嘌呤核苷酸交换因子5(ARHGEF5)相互作用,诱导RhoA活性和包括ROCK(Rho相关激酶)在内的下游因子的表达。 ODAM介导的RhoA信号传导导致肌动蛋白丝重排。整合素β3-和β6-敲除小鼠中ODAM和RhoA表达的降低表明,JE中的细胞骨架重组是通过整合素-ODAM-ARHGEF5-RhoA信号传导发生的。纤连蛋白和层粘连蛋白通过整联蛋白-ODAM途径激活RhoA信号传导。最后,在体内龈切除后,RhoA在再生的JE中用ODAM重新表达。这些结果表明,JE中的ODAM表达反映出健康的牙周膜,并且JE通过牙齿粘连蛋白/粘连蛋白-整联蛋白-ODAM-ARHGEF5-RhoA信号传导调节到牙齿表面的粘附。我们还建议ODAM可用作牙周炎和种植体周围炎的生物标志物。

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