Karbanová · Cells, tissues, organs 2011 · in vitro cell culture study · n=?

Characterization of dental pulp stem cells from impacted third molars cultured in low serum-containing medium.

Cited 111 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

In vitro bench study on human cell cultures.

PubMed 21071916 · doi:10.1159/000321160 · record verified 2026-08-30

What was done

Dental pulp stem cells (DPSCs) were isolated from extracted human impacted third molars and expanded in low serum-containing medium supplemented with epidermal growth factor (EGF) and platelet-derived growth factor BB (PDGF-BB). Differentiation potential was tested in adherent and micromass/spheroid cultures using osteogenic, chondrogenic (TGF-β1/3), endothelial (VEGF), and neurogenic induction media. Phenotypic marker expression in undifferentiated and differentiated cells was evaluated via flow cytometry, immunocytochemistry, and immunoblotting.

What was found

The abstract reports qualitative marker findings without numerical data. Undifferentiated DPSCs expressed mesenchymal stem cell markers and pluripotency/progenitor markers (Nanog, Sox2, nestin, Musashi-1, nucleostemin), but were negative for hematopoietic, neural, vascular, and hepatic differentiation markers. They exhibited weak α-smooth muscle actin expression and heterogeneous CD146 expression. Upon differentiation, DPSCs produced osteonectin, osteopontin, and procollagen I/collagen I (osteogenic), cartilaginous extracellular matrix (chondrogenic), endothelial markers (endothelial), and neural differentiation markers (neurogenic).

Why it matters

This study shows that accessible dental pulp from third molars can yield multipotent stem cells when cultured in low-serum conditions supplemented with growth factors, supporting their potential utility in tissue engineering.

Limits

The abstract provides no quantitative data or statistical comparisons. The number of donors or extracted teeth utilized is not reported. Differentiation was evaluated solely through in vitro marker expression rather than functional in vivo tissue formation.

Cited by