4.5 Article

Temporospatial Expression of Neuropeptide Substance P in Dental Pulp Stem Cells During Odontoblastic Differentiation in Vitro and Reparative Dentinogenesis in Vivo

Journal

JOURNAL OF ENDODONTICS
Volume 49, Issue 3, Pages 276-285

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.joen.2022.12.006

Keywords

Substance P; dental pulp stem cells; odontoblastic differentiation; reparative dentin

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This study investigated the expression and role of Substance P (SP) in reparative dentinogenesis. It was found that SP contributes to odontoblastic differentiation by binding to the neurokinin-1 receptor (NK1R). These findings provide important insights into the process of reparative dentin formation.
Introduction: Substance P (SP) is a neuropeptide released from the nervous fibers in response to injury. In addition to its association with pain and reactions to anxiety and stress, SP exerts various physiological functions by binding to the neurokinin-1 receptor (NK1R). However, the expression and role of SP in reparative dentinogenesis remain elusive. Here, we explored whether SP is involved in odontoblastic differentiation during reparative dentino-genesis. Methods: Dental pulp stem cells (DPSCs) were isolated from healthy human dental pulp tissues and subjected to odontoblastic differentiation. The expression of SP and NK1R during odontoblastic differentiation was investigated in vitro. The effects of SP on odontoblastic differentiation of DPSCs were evaluated using alizarin red staining, alkaline phosphatase staining, and real-time polymerase chain reaction. After direct pulp capping with mineral trioxide aggregate, the expression of SP and NK1R during reparative dentin formation in rats were identified using histological and immunohistochemical staining. Results: SP and NK1R expression increased during the odontoblastic differentiation of DPSCs. SP translocated to the nucleus when DPSCs were exposed to differentiation medium. NK1R was always present in the nuclei of DPSCs and odontoblast-like cells. Additionally, we discovered that 1028 M SP marginally enhanced the odontoblastic differentiation of DPSCs, and that these effects could be impaired by the NK1R antagonist. Furthermore, SP and NK1R were expressed in odontoblast-like and dental pulp cells during reparative dentin formation in vivo. Conclusions: SP contributes to odontoblastic differentiation during reparative dentin formation by binding to the NK1R. (J Endod 2023;49:276-285.)

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