Yang Xiaoting, Song Zhi, Chen Lingling, Wang Runfu, Huang Shuheng, Qin Wei, Guo Jia, Lin Zhengmei
Department of Operative Dentistry and Endodontics, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Guangdong 510055, P.R. China.
Guangdong Provincial Key Laboratory of Stomatology, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Guangdong 510055, P.R. China.
Exp Ther Med. 2017 Jul;14(1):73-78. doi: 10.3892/etm.2017.4471. Epub 2017 May 18.
Pulp capping is a restorative technique employed in an attempt to maintain pulpal vitality and generate reparative dentin. Ca released from capping materials is suggested to promote reparative dentin formation. Transient receptor potential channel 6 (TRPC6) is a receptor-operated Ca2+ channel that serves an important role in Ca2+ influx in the majority of non-excitable cells, and influences the calcium signaling and cell respond. Therefore, the purpose of the present study was to gain an insight into the role of TRPC6 in the odontoblastic differentiation of human dental pulp cells (HDPCs). Human dental pulp tissues and HDPCs were obtained from healthy third molars. By immunohistochemical staining, TRPC6 was observed to be highly expressed in the dental pulp tissue, particularly in the odontoblast layer. In addition, the protein level of TRPC6 was increased in a time-dependent manner during odontogenic differentiation of HDPCs. Downregulation of TRPC6 by a lentivirus vector containing TRPC6 shRNA inhibited the process of odontogenic differentiation in HDPCs. In conclusion, the current data demonstrated that TRPC6 served a significant role in the odontogenic differentiation of HDPCs, suggesting it may be a promising therapeutic target in regenerative endodontics.
盖髓术是一种修复技术,旨在维持牙髓活力并生成修复性牙本质。从盖髓材料中释放的钙被认为可促进修复性牙本质的形成。瞬时受体电位通道6(TRPC6)是一种受体操纵的Ca2+通道,在大多数非兴奋性细胞的Ca2+内流中起重要作用,并影响钙信号传导和细胞反应。因此,本研究的目的是深入了解TRPC6在人牙髓细胞(HDPCs)成牙本质细胞分化中的作用。人牙髓组织和HDPCs取自健康的第三磨牙。通过免疫组织化学染色,观察到TRPC6在牙髓组织中高表达,尤其是在成牙本质细胞层。此外,在HDPCs成牙分化过程中,TRPC6的蛋白水平呈时间依赖性增加。含有TRPC6 shRNA的慢病毒载体下调TRPC6可抑制HDPCs的成牙分化过程。总之,目前的数据表明TRPC6在HDPCs的成牙分化中起重要作用,提示它可能是再生牙髓病学中有前景的治疗靶点。