Yi Xiaosong, Wang Wei, Xie Qiufei
Department of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, China; Center for Oral Functional Diagnosis, Treatment and Research, Peking University School and Hospital of Stomatology, China.
Department of Stomatology, Shenzhen People's Hospital, Second Clinical Medical College of Jinan University, Shenzhen, Guangdong, China.
Biochem Biophys Res Commun. 2018 Mar 11;497(3):850-856. doi: 10.1016/j.bbrc.2018.02.125. Epub 2018 Feb 15.
Purinergic signaling regulates various biological processes through the activation of adenosine receptors (ARs) and P2 receptors. ATP induces the odontoblastic differentiation of human dental pulp cells (HDPCs) via P2 receptors. However, there is no information available about the roles of ARs in HDPC odontoblastic differentiation induced by ATP. Here, we found that HDPCs treated with ATP showed higher activity of ADORA1 (AR), ADORA2B (AR), and ADORA3 (AR). Inhibition of AR and AR attenuated ATP-induced odontoblastic differentiation of HDPCs, whereas activation of the two receptors enhanced the odontoblastic differentiation induced by ATP. However, activation of ARs by adenosine did not induce the odontoblastic differentiation of HDPCs independently without induction of ATP. Our study indicates a positive role for ARs in ATP-induced odontoblastic differentiation of HDPCs, and demonstrates that ATP-induced odontoblastic differentiation of HDPCs may be due to the combined administration of ARs and P2 receptors. This study provides new insights into the molecular mechanisms of pulpal injury repair induced by ATP.
嘌呤能信号通过激活腺苷受体(ARs)和P2受体来调节各种生物学过程。ATP通过P2受体诱导人牙髓细胞(HDPCs)的成牙本质细胞分化。然而,关于ARs在ATP诱导的HDPCs成牙本质细胞分化中的作用尚无相关信息。在此,我们发现用ATP处理的HDPCs表现出更高的ADORA1(AR)、ADORA2B(AR)和ADORA3(AR)活性。抑制AR和AR减弱了ATP诱导的HDPCs成牙本质细胞分化,而激活这两种受体则增强了ATP诱导的成牙本质细胞分化。然而,腺苷单独激活ARs在未诱导ATP的情况下并不能独立诱导HDPCs的成牙本质细胞分化。我们的研究表明ARs在ATP诱导的HDPCs成牙本质细胞分化中起积极作用,并证明ATP诱导的HDPCs成牙本质细胞分化可能是由于ARs和P2受体的联合作用。本研究为ATP诱导牙髓损伤修复的分子机制提供了新的见解。