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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 Peñarrochasubject
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 celldescription
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.
year | journal | country | edition | language |
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2014-10-01 | Stem Cell Reports |