Search results for "senescence."

showing 10 items of 335 documents

Attenuation of NF-κB Signaling Response to UVB Light during Cellular Senescence

1999

The ability of cells to adapt to environmental stresses undergoes a progressive reduction during aging. NF-kappaB-mediated signaling is a major defensive system against various environmental challenges. The aim of this study was to find out whether replicative senescence affects the response of the NF-kappaB signaling pathway to UVB light in human WI-38 and IMR-90 fibroblasts. The exposure of early passage fibroblasts to UVB light inhibited the proliferation and induced a flat phenotype similar to that observed in replicatively senescent fibroblasts not exposed to UVB light. The UVB radiation dose used (153 mJ/cm2) did not induce apoptosis in either early or late passage WI-38 fibroblasts. …

SenescenceP50Ultraviolet RaysLactams MacrocyclicBiologyCell LineBenzoquinonesHumansEnzyme InhibitorsProtein Kinase InhibitorsCellular SenescenceCell Line TransformedNF-kappa BQuinonesCell BiologyFibroblastsTyrphostinsMolecular biologyIκBαRifabutinApoptosisPhosphorylationTumor necrosis factor alphaSignal transductionNuclear localization sequenceSignal TransductionExperimental Cell Research
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An immunohistochemical study of the distribution of p 16 protein in oral mucosa in smokers, non-smokers and in frictional keratosis

2009

Objective: Our study aimed to characterize alteration in the immunohistochemical p16 expression in normal oral mucosa and non-neoplastic hyperproliferative disorders (i.e. frictional keratosis and mucosa from smokers). Study design: 43 specimen of oral mucosa were examined using immunohistochemistry. Results: In normal mucosa, there was strong positive nuclear staining in a proportion of fibroblasts and endothelial cells in the lamina propria, with variable expression in nuclei of the epithelial layer. However, when the patient?s tobacco smoking was examined, p16 nuclear staining in oral epithelium was seen in 4/20 (20%) of smokers and 0/23 (0%) of non-smokers. In every case of frictional k…

SenescencePathologymedicine.medical_specialtyKeratosisVariable ExpressionBasal (phylogenetics)medicineHumansDistribution (pharmacology)Oral mucosaGeneral DentistryCyclin-Dependent Kinase Inhibitor p16Lamina propriabusiness.industrySmokingMouth Mucosamedicine.disease:CIENCIAS MÉDICAS [UNESCO]ImmunohistochemistryNeoplasm Proteinsmedicine.anatomical_structureOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASImmunohistochemistrySurgeryLeukoplakia Oralbusiness
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Can Be miR-126-3p a Biomarker of Premature Aging? An Ex Vivo and In Vitro Study in Fabry Disease

2021

Fabry disease (FD) is a lysosomal storage disorder (LSD) characterized by lysosomal accumulation of glycosphingolipids in a wide variety of cytotypes, including endothelial cells (ECs). FD patients experience a significantly reduced life expectancy compared to the general population

SenescencePremature agingAdultMalesenescenceAdolescentPopulationsmall extracellular vesiclesUmbilical veinArticleAndrologyExtracellular VesiclesYoung AdultHUVECIn vivosmall extracellular vesicleHuman Umbilical Vein Endothelial CellsmiR-126-3pMedicineHumanseducationlcsh:QH301-705.5Cellular SenescenceAgedAged 80 and overSettore MED/04 - Patologia Generaleeducation.field_of_studySphingolipidsFabry diseasemicroRNAbusiness.industryagingAging PrematureGeneral MedicineMiddle Agedmedicine.diseaseFabry diseaseendothelial cellsMicroRNAslcsh:Biology (General)endothelial cellBiomarker (medicine)NanoparticlesFemaleGlycolipidsbusinessReactive Oxygen SpeciesEx vivoBiomarkersCells
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Proteomic analysis reveals a role for Bcl2-associated athanogene 3 and major vault protein in resistance to apoptosis in senescent cells by regulatin…

2014

Senescence is a prominent solid tumor response to therapy in which cells avoid apoptosis and instead enter into prolonged cell cycle arrest. We applied a quantitative proteomics screen to identify signals that lead to therapy-induced senescence and discovered that Bcl2-associated athanogene 3 (Bag3) is up-regulated after adriamycin treatment in MCF7 cells. Bag3 is a member of the BAG family of co-chaperones that interacts with Hsp70. Bag3 also regulates major cell-signaling pathways. Mass spectrometry analysis of the Bag3 Complex revealed a novel interaction between Bag3 and Major Vault Protein (MVP). Silencing of Bag3 or MVP shifts the cellular response to adriamycin to favor apoptosis. We…

SenescenceProteomicsCell cycle checkpointApoptosisBreast NeoplasmsBAG3BiochemistryAnalytical ChemistryMajor vault proteinCell Line TumorGene silencingHumansMolecular BiologyCellular SenescenceAdaptor Proteins Signal TransducingVault Ribonucleoprotein ParticlesMitogen-Activated Protein Kinase 1Antibiotics AntineoplasticMitogen-Activated Protein Kinase 3biologyResearchCell biologyApoptosisDoxorubicinbiology.proteinCancer researchSignal transductionApoptosis Regulatory ProteinsCell agingSignal TransductionMolecularcellular proteomics : MCP
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Npl3 stabilizes R-loops at telomeres to prevent accelerated replicative senescence.

2019

Abstract Telomere shortening rates must be regulated to prevent premature replicative senescence. TERRA R‐loops become stabilized at critically short telomeres to promote their elongation through homology‐directed repair (HDR), thereby counteracting senescence onset. Using a non‐bias proteomic approach to detect telomere binding factors, we identified Npl3, an RNA‐binding protein previously implicated in multiple RNA biogenesis processes. Using chromatin immunoprecipitation and RNA immunoprecipitation, we demonstrate that Npl3 interacts with TERRA and telomeres. Furthermore, we show that Npl3 associates with telomeres in an R‐loop‐dependent manner, as changes in R‐loop levels, for example, …

SenescenceProteomicssenescenceR-loopNpl3BiologyBiochemistryChromatin Epigenetics Genomics & Functional Genomics03 medical and health sciences0302 clinical medicineReportGeneticsMolecular BiologyCellular SenescenceTelomere Shortening030304 developmental biology0303 health sciencestelomereR‐loopRNAChromosomeRNA–DNA hybridTelomereCell biologyRna immunoprecipitationR-Loop StructuresChromatin immunoprecipitation030217 neurology & neurosurgeryBiogenesisReportsEMBO reports
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Vascular aging in rodent models: contrasting mechanisms driving the female and male vascular senescence

2021

Increasing scientific interest has been directed to sex as a biological and decisive factor on several diseases. Several different mechanisms orchestrate vascular function, as well as vascular dysfunction in cardiovascular and metabolic diseases in males and females. Certain vascular sex differences are present throughout life, while others are more evident before the menopause, suggesting two important and correlated drivers: genetic and hormonal factors. With the increasing life expectancy and aging population, studies on aging-related diseases and aging-related physiological changes have steeply grown and, with them, the use of aging animal models. Mouse and rat models of aging, the most…

SenescenceRodentbiologysex differenceagingRC952-954.6PhysiologyGeneral MedicineDOENÇAS CARDIOVASCULARES EM ANIMALvascular dysfunctionmedicine.diseaseMenopausevascular agingvascular senescenceGeriatricsbiology.animalmedicineLife expectancyVascular agingEndothelial dysfunctionHormoneVascular senescence
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The role of telomeres and telomerase in the senescence of postmitotic cells

2020

Senescence is a process related to the stopping of divisions and changes leading the cell to the SASP phenotype. Permanent senescence of many SASP cells contributes to faster aging of the body and development of age-related diseases due to the release of pro-inflammatory factors. Both mitotically active and non-dividing cells can undergo senescence as a result of activation of different molecular pathways. Telomeres, referred to as the molecular clock, direct the dividing cell into the aging pathway when reaching a critical length. In turn, the senescence of postmitotic cells depends not on the length of telomeres, but their functionality. Dysfunctional telomeres are responsible for trigger…

SenescenceTelomeraseDNA damageCellMitosisMitochondrionBiologySenescenceBiochemistry03 medical and health sciences0302 clinical medicinemedicineAnimalsHumansTelomeraseMolecular BiologyCellular Senescence030304 developmental biology0303 health sciencesKinaseCell BiologyTelomereCell biologyTelomereTelomeresmedicine.anatomical_structureCytoplasm030220 oncology & carcinogenesisDNA Repair
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Molecular regulation of lifespan extension in fertile ant workers.

2021

The evolution of sociality in insects caused a divergence in lifespan between reproductive and non-reproductive castes. Ant queens can live for decades, while most workers survive only weeks to a few years. In most organisms, longevity is traded-off with reproduction, but in social insects, these two life-history traits are positively linked. Once fertility is induced in workers, e.g. by queen removal, worker lifespan increases. The molecular regulation of this positive link between fecundity and longevity and generally the molecular underpinnings of caste-specific senescence are not well understood. Here, we investigate the transcriptomic regulation of lifespan and reproduction in fat bod…

SenescenceTemnothoraxbiologyTemnothorax rugatulusved/biologyAntsmedia_common.quotation_subjectved/biology.organism_classification_rank.speciesLongevityLongevityZoologyFertilityArticlesbiology.organism_classificationTrade-offFecundityGeneral Biochemistry Genetics and Molecular BiologyFertilityAnimalsGeneral Agricultural and Biological SciencesSocial BehaviorLife History TraitsSocialitymedia_commonPhilosophical transactions of the Royal Society of London. Series B, Biological sciences
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A Perspective on Aging in Rotifers

1980

Most research on aging in rotifers has been performed with populations, not with individuals. As a consequence, the dependent variable in these studies is usually either mean lifespan or rate of survivorship. After a brief consideration of the literature published since the last major review (King, 1969), the results of a series of experiments are presented. Males and females of three genetically distinct clones of Brachionus plicatilis were used for a factorial life table analysis at three different temperatures. The results of these experiments indicate several potential problems in using populations to study the aging process of individuals. These problems derive from the fact that lifes…

SenescenceVariablesbiologyLife tableEcologySurvivorship curvemedia_common.quotation_subjectPerspective (graphical)Brachionusbiology.organism_classificationDemographymedia_common
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BCL-xL, a Mitochondrial Protein Involved in Successful Aging: From C. elegans to Human Centenarians

2020

B-Cell Lymphoma-extra-large (BCL-xL) is involved in longevity and successful aging, which indicates a role for BCL-xL in cell survival pathway regulation. Beyond its well described role as an inhibitor of apoptosis by preventing cytochrome c release, BCL-xL has also been related, indirectly, to autophagy and senescence pathways. Although in these latter cases, BCL-xL has dual roles, either activating or inhibiting, depending on the cell type and the specific conditions. Taken together, all these findings suggest a precise mechanism of action for BCL-xL, able to regulate the crosstalk between apoptosis, autophagy, and senescence, thus promoting cell survival or cell death. All three pathways…

SenescenceautophagyAgingProgrammed cell deathsenescencemedia_common.quotation_subjectbcl-X ProteinBcl-xLReviewMitochondrionInhibitor of apoptosisCatalysislcsh:ChemistryMitochondrial ProteinsInorganic Chemistry03 medical and health sciences0302 clinical medicinelongevityAnimalsHumansPhysical and Theoretical ChemistryCaenorhabditis eleganslcsh:QH301-705.5Molecular BiologySpectroscopy030304 developmental biologymedia_commonAged 80 and over0303 health sciencesbiologyOrganic ChemistryAutophagyapoptosisLongevityGeneral MedicineComputer Science ApplicationsCell biologymitochondriaCrosstalk (biology)lcsh:Biology (General)lcsh:QD1-999healthy aging030220 oncology & carcinogenesisbiology.proteinFisiologia humanaInternational Journal of Molecular Sciences
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