Wongkhantee S, Yongchaitrakul T, Pavasant P
Department of Anatomy, Graduate School of Oral Biology, Faculty of Dentistry, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
J Dent Res. 2008 Jun;87(6):564-8. doi: 10.1177/154405910808700601.
Our previous study showed that mechanical stress induced the expression of osteopontin (OPN) in human periodontal ligament (HPDL) cells through the Rho kinase pathway. The increase of OPN expression via Rho kinase has been demonstrated to be triggered by nucleotide. Therefore, we hypothesized that nucleotides, particularly adenosine triphosphate (ATP), participated in the stress-induced OPN expression in HPDL cells. In the present study, the roles of ATP and P2Y1 purinoceptor were examined. Reverse-transcription polymerase chain-reaction and Western blot analysis revealed that the stress-induced ATP exerted its stimulatory effect on OPN expression. The inductive effect was attenuated by apyrase and completely inhibited by the Rho kinase inhibitor, as well as by the P2Y1 antagonist. We here propose that stress induces release of ATP, which in turn mediates Rho kinase activation through the P2Y1 receptor, resulting in the up-regulation of OPN. Stress-induced ATP could play a significant role in alveolar bone resorption.
我们之前的研究表明,机械应力通过Rho激酶途径诱导人牙周膜(HPDL)细胞中骨桥蛋白(OPN)的表达。已证明通过Rho激酶增加OPN表达是由核苷酸触发的。因此,我们推测核苷酸,特别是三磷酸腺苷(ATP),参与了HPDL细胞中应力诱导的OPN表达。在本研究中,检测了ATP和P2Y1嘌呤受体的作用。逆转录聚合酶链反应和蛋白质印迹分析表明,应力诱导的ATP对OPN表达发挥刺激作用。这种诱导作用被腺苷三磷酸双磷酸酶减弱,并被Rho激酶抑制剂以及P2Y1拮抗剂完全抑制。我们在此提出,应力诱导ATP释放,进而通过P2Y1受体介导Rho激酶激活,导致OPN上调。应力诱导的ATP可能在牙槽骨吸收中起重要作用。