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A Putative Association of a Single Nucleotide Polymorphism in GPR126 with Aggressive Periodontitis in a Japanese Population

机译:推测的GPR126中的单核苷酸多态性与侵略性牙周炎在日本人口中的关联。

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摘要

Periodontitis is an inflammatory disease causing loss of tooth-supporting periodontal tissue. Disease susceptibility to the rapidly progressive form of periodontitis, aggressive periodontitis (AgP), appears to be influenced by genetic risk factors. To identify these in a Japanese population, we performed whole exome sequencing of 41 unrelated generalized or localized AgP patients. We found that AgP is putatively associated with single nucleotide polymorphism (SNP) rs536714306 in the G-protein coupled receptor 126 gene, GPR126 [c.3086 G>A (p.Arg1029Gln)]. Since GPR126 activates the cAMP/PKA signaling pathway, we performed cAMP ELISA analysis of cAMP concentrations, and found that rs536714306 impaired the signal transactivation of GPR126. Moreover, transfection of human periodontal ligament (HPDL) cells with wild-type or mutant GPR126 containing rs536714306 showed that wild-type GPR126 significantly increased the mRNA expression of bone sialoprotein, osteopontin, and Runx2 genes, while mutant GPR126 had no effect on the expression of these calcification-related genes. The increase in expression of these genes was through the GPR126-induced increase of bone morphogenic protein-2, inhibitor of DNA binding (ID) 2, and ID4 expression. These data indicate that GPR126 might be important in maintaining the homeostasis of periodontal ligament tissues through regulating the cytodifferentiation of HPDL cells. The GPR126 SNP rs536714306 negatively influences this homeostasis, leading to the development of AgP, suggesting that it is a candidate genetic risk factor for AgP in the Japanese population.
机译:牙周炎是引起牙齿支撑牙周组织损失的炎性疾病。疾病对牙周炎快速进展型,侵袭性牙周炎(AgP)的易感性似乎受遗传危险因素的影响。为了在日本人群中鉴定这些基因,我们对41名不相关的全身或局部AgP患者进行了完整的外显子组测序。我们发现,AgP可能与G蛋白偶联受体126基因GPR126中的单核苷酸多态性(SNP)rs536714306相关[c.3086 G> A(p.Arg1029Gln)]。由于GPR126激活cAMP / PKA信号通路,因此我们对cAMP浓度进行了cAMP ELISA分析,发现rs536714306损害了GPR126的信号反式激活。此外,用含有rs536714306的野生型或突变型GPR126转染人牙周膜(HPDL)细胞显示,野生型GPR126显着增加了骨唾液蛋白,骨桥蛋白和Runx2基因的mRNA表达,而突变型GPR126对表达却没有影响这些钙化相关基因。这些基因表达的增加是通过GPR126诱导的骨形态发生蛋白2,DNA结合抑制剂(ID)2和ID4表达的增加。这些数据表明,GPR126可能通过调节HPDL细胞的细胞分化,在维持牙周膜组织的稳态中很重要。 GPR126 SNP rs536714306对这种稳态产生负面影响,导致AgP的发展,表明它是日本人群中AgP的候选遗传危险因素。

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