6533b7d8fe1ef96bd126a4cd

RESEARCH PRODUCT

Activation of p38, p21, and NRF-2 Mediates Decreased Proliferation of Human Dental Pulp Stem Cells Cultured under 21% O2

Giovanni E. MannJuan GambiniRichard C.m. SiowJose ViñaJose Viña-almuniaMarya El AlamiConsuelo BorrasCristina Mas-barguesMiguel Peñarrocha

subject

MaleAdolescentNF-E2-Related Factor 2Biologymedicine.disease_causep38 Mitogen-Activated Protein KinasesBiochemistryYoung AdultDownregulation and upregulationReportDental pulp stem cellsGeneticsmedicineHumanslcsh:QH301-705.5Cells CulturedDental PulpCell Proliferationchemistry.chemical_classificationReactive oxygen specieslcsh:R5-920Cell growthCell BiologyCell biologyOxygenAdult Stem CellsOxidative Stressp21-Activated Kinaseschemistrylcsh:Biology (General)ImmunologySignal transductionStem celllcsh:Medicine (General)Oxidative stressDevelopmental BiologyAdult stem cell

description

Summary High rates of stem cell proliferation are important in regenerative medicine and in stem cell banking for clinical use. Ambient oxygen tensions (21% O2) are normally used for in vitro culture, but physiological levels in vivo range between 3% and 6% O2. We compared proliferation of human dental pulp stem cells (hDPSCs) cultured under 21% versus 3% O2. The rate of hDPSC proliferation is significantly lower at 21% O2 compared to physiological oxygen levels due to enhanced oxidative stress. Under 21% O2, increased p38 phosphorylation led to activation of p21. Increased generation of reactive oxygen species and p21 led to activation of the NRF-2 signaling pathway. The upregulation of NRF-2 antioxidant defense genes under 21% O2 may interact with cell-cycle-related proteins involved in regulating cell proliferation. Activation of p38/p21/NRF-2 in hDPSCs cultured under ambient oxygen tension inhibits stem cell proliferation and upregulates NRF-2 antioxidant defenses.

10.1016/j.stemcr.2014.08.002http://www.sciencedirect.com/science/article/pii/S221367111400246X