Introduction The repair of dental pulp injury is the cornerstone of vital pulp therapy. Traditional research has predominantly focused on the roles of immune cells, vascular endothelial cells, and dental pulp stem cells, often overlooking the active regulatory functions of the sensory neural network. Sensory nerve fibers constitute nearly 40% of the dental pulp volume, and their released neuropeptides, such as calcitonin Gene-Related Peptide (CGRP), are hypothesized to coordinate the repair process via intercellular communication. This study aims to systematically elucidate the molecular mechanisms by which sensory nerves and their key neuropeptide, CGRP, regulate angiogenesis and the activation of stromal cells within the injured pulp microenvironment, thereby providing a theoretical basis for novel pulp regeneration strategies targeting neural signaling pathways. Methods The cell-cell communication network in dental pulp was using single-cell transcriptome analysis (GSE197289, GSE274562, GSE280528). A series of in vitrocellular experiments, including qPCR, Western blot, immunofluorescence, scratch wound healing assay, and tube formation assay, were employed to evaluate the effects of CGRP on cell migration, angiogenesis, and mineralization. A mouse model of dentin-pulp injury was established, and the in vivoangiogenic changes were validated through intervention with the CGRP receptor antagonist BIBN4096BS. RNA sequencing was conducted to analyze the transcriptional reprogramming of human dental pulp cells (DPCs) induced by CGRP. Results Single-cell communication analysis revealed intensive CGRP signaling interactions between sensory neurons, endothelial cells, and dental pulp cells. In vitroexperiments demonstrated that CGRP directly enhanced the tube-forming and migratory capabilities of human umbilical vein endothelial cells (HUVECs) and upregulated the expression of CD31/VEGFA. Furthermore, CGRP potentiated the mineralization of dental Pulp Stem Cells (DPSCs) via a paracrine mechanism. Concurrently, CGRP significantly accelerated the migration of DPCs, and the conditioned medium from CGRP-pretreated DPCs enhanced endothelial tube formation, a mechanism involving the upregulation of VEGFA and the activation of IL-17/TNF signaling pathways. In vivoexperiments confirmed that inhibition of CGRP signaling significantly reduced angiogenesis (CD31 + signals) in the injured pulp area of mice. Conclusion This study elucidates that the sensory neuropeptide CGRP drives a “neuro-vascular-stromal cell” collaborative network during pulp repair through dual pathways: directly activating endothelial cell function and indirectly modulating the paracrine profile of dental pulp cells (e.g., upregulating VEGFA), thereby promoting angiogenesis and stem cell differentiation. This discovery not only deepens the understanding of the self-repair mechanisms of dental pulp but also offers a new perspective for developing precise vital pulp therapy strategies targeting CGRP signaling, such as modulating the neuro-microenvironment interaction.
Wu et al. (Tue,) studied this question.