Search results for " Repair"

showing 10 items of 721 documents

DNA damage causes TP53-dependent coupling of self-renewal and senescence pathways in embryonal carcinoma cells.

2013

Recent studies have highlighted an apparently paradoxical link between self-renewal and senescence triggered by DNA damage in certain cell types. In addition, the finding that TP53 can suppress senescence has caused a re-evaluation of its functional role in regulating these outcomes. To investigate these phenomena and their relationship to pluripotency and senescence, we examined the response of the TP53-competent embryonal carcinoma (EC) cell line PA-1 to etoposide-induced DNA damage. Nuclear POU5F1/OCT4A and P21CIP1 were upregulated in the same cells following etoposide-induced G 2M arrest. However, while accumulating in the karyosol, the amount of OCT4A was reduced in the chromatin fract…

SenescenceCyclin-Dependent Kinase Inhibitor p21OCT4A/POU5F1Embryonal Carcinoma Stem CellssenescenceDNA RepairDNA repairDNA damagetumor cellsBiologyProtein Serine-Threonine Kinasesself-renewalHistonesAurora KinasesCell Line TumorReportAutophagyAurora Kinase BHumansTP53PhosphorylationRNA Small InterferingMolecular BiologyMitosisCellular SenescenceCyclin-Dependent Kinase Inhibitor p16EtoposideOvarian NeoplasmsEmbryonal Carcinoma Stem CellsCell BiologyG2-M DNA damage checkpointbeta-GalactosidasepluripotencyAntineoplastic Agents PhytogenicChromatinUp-RegulationG2 Phase Cell Cycle CheckpointsCheckpoint Kinase 2Cancer researchDNA damageFemaleRNA InterferenceRad51 RecombinaseTumor Suppressor Protein p53Cell agingOctamer Transcription Factor-3Developmental BiologyCell cycle (Georgetown, Tex.)
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Long-term effects of delayed parenthood.

1998

The present study aims to define, characterize and compare the long-term effects on offspring of delayed parenthood. Data published so far on this topic show that maternal and paternal ageing may affect offspring by different mechanisms. Delayed motherhood is characterized by increased probability of obstetric complications and/or fetal and perinatal problems which, in turn, may increase the risks of mortality and morbidity in newborns and later life. Furthermore, maternal ageing is distinguished by a decreased ratio of male to female infants and higher odds of conceiving a trisomic child and/or an individual suffering from mitochondrial DNA disorders. In contrast, delayed fatherhood is ass…

SenescenceMaleMitochondrial DNAmedicine.medical_specialtyDNA RepairOffspringDiseaseBiologymedicine.disease_causePaternal AgeAndrologyPregnancyInternal medicinemedicineHumansFetusPregnancyRehabilitationPregnancy OutcomeObstetrics and Gynecologymedicine.diseasePregnancy ComplicationsEndocrinologyReproductive MedicineAgeingMutationFemaleOxidative stressMaternal AgeHuman reproduction (Oxford, England)
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The role of mitochondrial oxidative stress in aging.

2003

Mitochondria are both a major source of oxidants and a target for their damaging effects, and, therefore, mitochondrial oxidative stress appears to be a cause, rather than a consequence, of cell aging. Oxidative damage in aging is particularly high in specific molecular targets, such as mitochondrial DNA and aconitase, and mitochondrial oxidative stress may drive tissue aging through intrinsic apoptosis. Mitochondrial function and morphology are impaired upon aging, as judged by a decline in membrane potential as well as by an increase in peroxide production and size of the organelles. In view of the age-related decreases in mitochondrial protein synthesis, mitochondrial transcripts, and ex…

SenescenceMitochondrial DNAAgingDNA RepairMitochondrial TurnoverMitochondrionBiologymedicine.disease_causeBiochemistryDNA MitochondrialGlutathioneMitochondriaOxygenOxidative StressBiochemistrymitochondrial fusionLiverPhysiology (medical)medicineDNAJA3AnimalsHumansReactive Oxygen SpeciesCell agingOxidative stressFree radical biologymedicine
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Isolation of cell clones from stem cell population more resistant to oxidative stress for tissue repair.

2012

Settore BIO/06 - Anatomia Comparata E Citologiastem cell tissue repair cell clones oxidative stress
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Perinatal and Wharton's jelly-derived mesenchymal stem cells in cartilage regenerative medicine and tissue engineering strategies

2011

Stem cells can be found in embryonic and extraembryonic tissues as well as in adult organs. In particular, research in the last few years has delineated the key features of perinatal stem cells derived from fetus-associated tissues. These cells show multiple differentiation potential, can be easily expanded ex vivo, and raise no ethical concerns as regards their use. Several reports indicate that cells isolated from Wharton's jelly (WJ), the main component of umbilical cord extracellular matrix, are multipotent stem cells that express markers shared by other mesenchymal stem cells (MSC) and give rise to different mature cell types belonging to all three germ layers. Moreover, WJ-MSC display…

Settore BIO/16 - Anatomia UmanaMesenchymal stem cellClinical uses of mesenchymal stem cellsBiologyRegenerative medicineCell biologyDevelopmental NeuroscienceMultipotent Stem CellWharton's jellyImmunologyArticular cartilage Chondrocytes Differentiation markers Extracellular matrix Mesenchymal stem cells scaffolds Tissue engineering Umbilical cord Wharton’s jellyStem cellDevelopmental BiologyStem cell transplantation for articular cartilage repairAdult stem cell
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Wharton's Jelly Mesenchymal Stem Cells and Immune Modulation: Regenerative Medicine Meets Tissue Repair

2013

Settore BIO/16 - Anatomia UmanaMesenchymal stem cellImmunologyWharton's jellyBiologyTissue repairImmune modulationRegenerative medicineWharton's jelly umbilical cord mesenchymal stem cells regenerative medicine immune modulation tissue repair differentiationCell biology
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New frontiers in regenerative medicine in cardiology: the potential of Wharton's jelly mesenchymal stem cells.

2013

Cardiomyopathies are still the first cause of death in the world. The identification of resident stem cells, comprising those derived from sub-endocardial stroma, suggests the possible self regeneration of the heart under autocrine/paracrine modulation in the cardiac microenvironment. Nevertheless, because of the limited in vivo regeneration potential of damaged cardiac tissue, the use of drugs and ultimately cardiac transplantation remain the common treatments of heart diseases and defects. The differentiative potential of embryonic and mesenchymal stem cells (MSCs) derived from different tissues (such as bone marrow and adipose tissue) was extensively explored in cell therapy for regenera…

Settore BIO/17 - IstologiaImmune modulationCardiologyMedicine (miscellaneous)Clinical uses of mesenchymal stem cellsHeart failureBiologyRegenerative MedicineRegenerative medicineWharton's jellyHumansWharton JellyTissue repairMesenchymal stem cellStem cell transplantation for articular cartilage repairSettore BIO/16 - Anatomia UmanaWharton's jellyRegeneration (biology)Mesenchymal stem cellMesenchymal Stem CellsGeneral MedicineHeart failure; Immune modulation; Mesenchymal stem cells; Regenerative medicine; Tissue repair; Wharton's jellyTransplantationCardiovascular DiseasesImmunologyCancer researchStem cell
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Current Perspectives on Adult Mesenchymal Stromal Cell-Derived Extracellular Vesicles: Biological Features and Clinical Indications.

2022

Extracellular vesicles (EVs) constitute one of the main mechanisms by which cells communicate with the surrounding tissue or at distance. Vesicle secretion is featured by most cell types, and adult mesenchymal stromal cells (MSCs) of different tissue origins have shown the ability to produce them. In recent years, several reports disclosed the molecular composition and suggested clinical indications for EVs derived from adult MSCs. The parental cells were already known for their roles in different disease settings in regulating inflammation, immune modulation, or transdifferentiation to promote cell repopulation. Interestingly, most reports also suggested that part of the properties of pare…

Settore BIO/17 - Istologiaadult mesenchymal stromal cellsbone marrowinflammationregenerationcell-free therapiescancerMedicine (miscellaneous)tissue repairextracellular vesiclesGeneral Biochemistry Genetics and Molecular Biologyadipose tissueBiomedicines
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Gene amplification in fibroblasts from ataxia telangiectasia (AT) patients and in X-ray hypersensitive AT-like Chinese hamster mutants

2001

In search of functions involved in the regulation of gene amplification, and given the relevance of chromosome breakage in initiating the process, we analyzed the gene amplification ability of cells hypersensitive to inducers of DNA double-strand breaks and defective in cell cycle control: two human fibroblast strains derived from patients affected by ataxia telangiectasia (AT) and two hamster mutant cell lines belonging to complementation group XRCC8 of the rodent X-ray-sensitive mutants. These mutants are considered hamster models of AT cells. To measure gene amplification, the frequency and the rate of occurrence of N-(phosphonacetyl)-l-aspartate resistant cells were determined. In both …

Settore BIO/18 - GeneticaCancer Research gene amplification DNA repair
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EXPERIMENTAL ANALYSIS OF SMALL CLAY BRICK CYLINDERS CONFINED BY BFRP GRID UNDER AXIAL COMPRESSION

2019

Many investigations have shown that fibre reinforced polymer (FRP) composites can be effectively used to induce a passive confinement action on masonry columns and improve their axial capacity and ductility. This paper presents the results of an experimental study on the compressive behaviour of clay brick masonry cylinders externally wrapped with basalt fiber reinforced polymer (BFRP) grids. The circular section shape was chosen to assess the pure confinement effect on the masonry material. Fourteen clay brick masonry cylinders, cored from two different masonry assembly types, were confined with one or two layers of BFRP grids. The two assemblies were used to investigate the effect of vert…

Settore ICAR/09 - Tecnica Delle CostruzioniBFRPMasonry columnBasalt Fibre Reinforced PolymerStrengthening and Repair.
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