Ontology highlight
ABSTRACT: Background
Dental pulp stem cells (DPSCs) are increasingly being advocated as viable cell sources for regenerative medicine-based therapies. However, significant heterogeneity in DPSC expansion and multi-potency capabilities are well-established, attributed to contrasting telomere profiles and susceptibilities to replicative senescence. As DPSCs possess negligible human telomerase (hTERT) expression, we examined whether intrinsic differences in the susceptibilities of DPSC sub-populations to oxidative stress-induced biomolecular damage and premature senescence further contributed to this heterogeneity, via differential enzymic antioxidant capabilities between DPSCs.Methods
DPSCs were isolated from human third molars by differential fibronectin adhesion, and positive mesench
SUBMITTER: Alaidaroos NYA
PROVIDER: S-EPMC7890809 | biostudies-literature | 2021 Feb
REPOSITORIES: biostudies-literature