Search results for "premature senescence"

showing 3 items of 3 documents

Role of p16INK4a and BMI-1 in oxidative stress-induced premature senescence in human dental pulp stem cells

2017

Human dental pulp stem cells (hDPSCs) are a source for cell therapy. Before implantation, an in vitro expansion step is necessary, with the inconvenience that hDPSCs undergo senescence following a certain number of passages, loosing their stemness properties. Long-term in vitro culture of hDPSCs at 21% (ambient oxygen tension) compared with 3–6% oxygen tension (physiological oxygen tension) caused an oxidative stress-related premature senescence, as evidenced by increased β-galactosidase activity and increased lysil oxidase expression, which is mediated by p16INK4a pathway. Furthermore, hDPSCs cultured at 21% oxygen tension underwent a downregulation of OCT4, SOX2, KLF4 and c-MYC factors, w…

AdultMale0301 basic medicineSenescenceAginghDPSCs human dental pulp stem cellsMSC mesenchymal stem cellsAdolescentCellular differentiationClinical BiochemistryCell Culture TechniquesOSKM OCT4 SOX2 KLF4 and c-MYCBiologymedicine.disease_causeBiochemistryCell therapyKruppel-Like Factor 4Young Adult03 medical and health sciencesDental pulp stem cellsmedicineHumansOxygen tensionlcsh:QH301-705.5SIPS stress-induced premature senescenceCells CulturedCellular SenescenceCyclin-Dependent Kinase Inhibitor p16Dental PulpMDA malondialdehydePolycomb Repressive Complex 1lcsh:R5-920Stem CellsOrganic ChemistryCell DifferentiationOxygen tensionCell biologyOxygenOxidative Stress030104 developmental biologylcsh:Biology (General)Cell cultureRegenerative medicineImmunologyFemaleStem celllcsh:Medicine (General)Oxidative stressResearch PaperRedox Biology
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Calorie Restriction in Adulthood Reduces Hepatic Disorders Induced by Transient Postnatal Overfeeding in Mice

2019

International audience; Impaired early nutrition influences the risk of developing metabolic disorders in later life. We observed that transient postnatal overfeeding (OF) in mice induces long-term hepatic alterations, characterized by microsteatosis, fibrosis associated with oxidative stress (OS), and stress-induced premature senescence (SIPS). In this study, we investigated whether such changes can be reversed by moderate calorie restriction (CR). C57BL/6 male mice pups were maintained during lactation in litters adjusted to nine pups in the normal feeding (NF) group and three pups in the transient postnatal OF group. At six months of age, adult mice from the NF and OF groups were randoml…

Male0301 basic medicineStress-induced premature senescencemedicine.disease_causeMicechemistry.chemical_compound0302 clinical medicineFibrosisLactationoxidative stressCellular Senescence2. Zero hungerNutrition and DieteticsbiologySuperoxideLiver DiseasesDOHaDCatalasemedicine.anatomical_structure030220 oncology & carcinogenesisstress-induced premature senescenceFemalelcsh:Nutrition. Foods and food supplymedicine.medical_specialtyAnimals; Animals Newborn; Caloric Restriction/methods; Catalase/metabolism; Cellular Senescence; Feeding Methods/adverse effects; Female; Liver/metabolism; Liver Diseases/diet therapy; Liver Diseases/etiology; Liver Diseases/physiopathology; Male; Mice; Mice Inbred C57BL; Oxidative Stress; Superoxide Dismutase/metabolism; DOHaD; developmental programming; liver; oxidative stress; reversibility; stress-induced premature senescenceCalorie restrictionlcsh:TX341-641liverArticleLipofuscinFeeding MethodsSuperoxide dismutase03 medical and health sciencesreversibility[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular systemdevelopmental programmingInternal medicinemedicineAnimalsCaloric RestrictionSuperoxide Dismutasebusiness.industrymedicine.diseaseMice Inbred C57BL030104 developmental biologyEndocrinologyAnimals Newbornchemistrybiology.proteinbusinessOxidative stressFood Science
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Stress induced premature liver senecence in adulthood after transient postnatal overfeeding in mice

2017

IF 2.043; International audience

premature senescence[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular systemSIRT1 deficiency[ SDV.MHEP.CSC ] Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system[SDV.MHEP.CSC] Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system
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