Postnatal human dental pulp stem cells (DPSCs) <i>in vitro</i> and <i>in</i> <i>vivo</i>

TLDR

Dentinal repair in postnatal organisms relies on odontoblasts, whose precursor population within pulp tissue remains undefined. The study aimed to isolate a clonogenic, rapidly proliferative dental pulp stem cell (DPSC) population from adult human pulp. Isolated DPSCs were compared to human bone marrow stromal cells (BMSCs) to assess their differentiation potential. Functional assays showed that DPSCs formed sporadic, densely calc.

Abstract

Dentinal repair in the postnatal organism occurs through the activity of specialized cells, odontoblasts, that are thought to be maintained by an as yet undefined precursor population associated with pulp tissue. In this study, we isolated a clonogenic, rapidly proliferative population of cells from adult human dental pulp. These DPSCs were then compared with human bone marrow stromal cells (BMSCs), known precursors of osteoblasts. Although they share a similar immunophenotype in vitro, functional studies showed that DPSCs produced only sporadic, but densely calcified nodules, and did not form adipocytes, whereas BMSCs routinely calcified throughout the adherent cell layer with clusters of lipid-laden adipocytes. When DPSCs were transplanted into immunocompromised mice, they generated a dentin-like structure lined with human odontoblast-like cells that surrounded a pulp-like interstitial tissue. In contrast, BMSCs formed lamellar bone containing osteocytes and surface-lining osteoblasts, surrounding a fibrous vascular tissue with active hematopoiesis and adipocytes. This study isolates postnatal human DPSCs that have the ability to form a dentin/pulp-like complex.