# Extracellular Vesicles Derived from Human CD24+ Dental Papilla Stem Cells Promote Vascularized Dental Pulp Regeneration

## TL;DR

Extracellular vesicles from a specific type of dental stem cells can regenerate dental pulp and promote blood vessel formation, offering a new regenerative therapy for dentistry.

## Contribution

The study demonstrates that CD24+ EVs from dental papilla stem cells can regenerate vascularized pulp-like tissue.

## Key findings

- CD24+ EVs enhance proliferation, migration, and odontogenic differentiation of dental pulp stem cells in vitro.
- CD24+ EVs promote endothelial tube formation and robust angiogenesis in a regeneration model.
- CD24+ EVs induce formation of well-organized, vascularized pulp-like tissue with DSPP expression.

## Abstract

Pulp necrosis remains a significant clinical challenge in dentistry, as current therapeutic approaches fail to achieve functional pulp regeneration. Extracellular vesicles (EVs), as crucial mediators of intercellular communication, offer new opportunities for regenerative strategies. In this study, we focus on CD24+ human dental papilla cells (CD24+ hDPCs), a functionally defined subpopulation previously characterized as having superior regenerative potential, and evaluate the regenerative potential of their derived EVs (CD24+ EVs) in pulp-like tissue regeneration. CD24+ EVs significantly enhanced the proliferation, migration, and osteo/odontogenic differentiation of human dental pulp stem cells (hDPSCs) and markedly promoted endothelial tube formation in vitro. In a treated dentin matrix (TDM)-based ectopic regeneration model, CD24+ EVs increased cellular accumulation within the regenerated tissue and robust angiogenesis, inducing the formation of well-organized, highly vascularized pulp-like tissue with dense cellular architecture and positive DSPP expression. Together, these findings suggest that CD24+ EVs concurrently enhance cell migration, odontogenic differentiation, and angiogenesis, and support a promising cell-assisted EV strategy grounded in functionally defined cellular subpopulations for pulp-like tissue regeneration.