Search results for " STEM CELLS"

showing 10 items of 881 documents

Effect of LIF-withdrawal on acetylcholine synthesis in the embryonic stem cell line CGR8 is not mediated by STAT3, PI3Ks or cAMP/PKA pathways.

2015

Acetylcholine (ACh) acts as a local cellular signaling molecule and is widely expressed in nature, including mammalian cells and embryonic stem cells. The murine embryonic stem cell line CGR8 synthesizes and releases substantial amounts of ACh. Particularly during early differentiation - a period associated with multiple alterations in geno-/phenotype functions - synthesis and release of ACh are increased by 10-fold. In murine stem cells second messengers of the STAT-3, PI3K and cAMP/PKA pathways are involved in maintaining self-renewal and pluripotency. The present experiments were designed to test whether blockers of these signaling pathways enhance ACh cell content in the presence of LIF…

STAT3 Transcription FactorCell signalingCurcuminMorpholinesImmunologyBiologyLeukemia Inhibitory FactorGene Expression Regulation Enzymologicchemistry.chemical_compoundMicePhosphatidylinositol 3-KinasesCyclic AMPImmunology and AllergyAnimalsLY294002PI3K/AKT/mTOR pathwayEmbryonic Stem CellsPharmacologySulfonamidesForskolinColforsinIsoquinolinesEmbryonic stem cellCyclic AMP-Dependent Protein KinasesAcetylcholineCell biologychemistryChromonesSecond messenger systemSignal transductionStem cellSignal TransductionInternational immunopharmacology
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Channeled scaffolds implanted in adult rat brain.

2012

Scaffolds with aligned channels based on acrylate copolymers, which had previously demonstrated good com- patibility with neural progenitor cells were studied as coloniz- able structures both in vitro with neural progenitor cells and in vivo, implanted without cells in two different locations, in the cortical plate of adult rat brains and close to the subven- tricular zone. In vitro, neuroprogenitors colonize the scaffold and differentiate into neurons and glia within its channels. When implanted in vivo immunohistochemical analysis by confocal microscopy for neural and endothelial cells markers demonstrated that the scaffolds maintained continuity with the surrounding neural tissue and wer…

ScaffoldAgingMaterials scienceAngiogenesisbrainBiomedical EngineeringSubventricular zoneNeovascularization PhysiologicScaffold SeedingNeural tissue engineeringGlial scarScaffoldBiomaterialsangiogenesisbiocompatibilityImplants ExperimentalNeural Stem CellsIn vivomedicineAnimalsRats WistarCerebral CortexNeuronsTissue ScaffoldsMetals and AlloysBrainCell DifferentiationNeural stem cellRatsAdult Stem Cellsmedicine.anatomical_structureMicroscopy FluorescenceMAQUINAS Y MOTORES TERMICOSCeramics and CompositesMicroscopy Electron ScanningFemaleneural regenerationNeurogliaBiomedical engineeringStem Cell TransplantationJournal of biomedical materials research. Part A
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Mesenchymal and Induced Pluripotent Stem Cells-Derived Extracellular Vesicles: The New Frontier for Regenerative Medicine?

2020

Regenerative medicine aims to repair damaged, tissues or organs for the treatment of various diseases, which have been poorly managed with conventional drugs and medical procedures. To date, multimodal regenerative methods include transplant of healthy organs, tissues, or cells, body stimulation to activate a self-healing response in damaged tissues, as well as the combined use of cells and bio-degradable scaffold to obtain functional tissues. Certainly, stem cells are promising tools in regenerative medicine due to their ability to induce de novo tissue formation and/or promote organ repair and regeneration. Currently, several studies have shown that the beneficial stem cell effects, espec…

ScaffoldInduced Pluripotent Stem Cellsregenerative medicineStimulationReviewBiologyRegenerative medicineExtracellular VesiclesParacrine signallingstem cellsAnimalsHumansInduced pluripotent stem celllcsh:QH301-705.5mesenchymal stem cells (MSCs)Regeneration (biology)Mesenchymal stem cellBiological TransportMesenchymal Stem CellsGeneral MedicineCell biologylcsh:Biology (General)induced pluripotent stem cells (iPSCs)extracellular vesicleStem cellStem Cell TransplantationCells
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Production of a Double-Layer Scaffold for the “On-Demand” Release of Fibroblast-like Limbal Stem Cells

2019

The production and characterization of a double layer scaffold, to be used as a system for the “on demand” release of corneal limbal stem cells are here reported. The devices used in the clinics and proposed so far in the scientific literature, for the release of corneal stem cells in the treatment of limbal stem cell deficiency, cannot control the in vivo space-time release of cells since the biomaterial of which they are composed is devoid of stimuli responsiveness features. Our approach was to produce a scaffold composed of two different polymeric layers that give the device the appropriate mechanical properties to be placed on the ocular surface and the possibility of releasing the stem…

ScaffoldMaterials sciencePolyestersFibroblast-like limbal stem cells Limbal stem cells deficiency On demand cell releasing systems Electrospun scaffold Hyaluronic acid based film coatingBiocompatible Materials02 engineering and technologyLimbus CorneaeLimbal stem cell deficiencyCornea03 medical and health sciences0302 clinical medicineCell Line TumorOn demandmedicineHumansGeneral Materials ScienceFibroblastCells CulturedDouble layer (biology)Stem CellsEpithelium CornealEpithelial CellsFibroblasts021001 nanoscience & nanotechnologyeye diseasesCell biologymedicine.anatomical_structureSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoMicroscopy Electron Scanning030221 ophthalmology & optometrysense organsStem cell0210 nano-technologyStem Cell TransplantationACS Applied Materials & Interfaces
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Characterization of the complete fiber network topology of planar fibrous tissues and scaffolds

2010

Understanding how engineered tissue scaffold architecture affects cell morphology, metabolism, phenotypic expression, as well as predicting material mechanical behavior has recently received increased attention. In the present study, an image-based analysis approach that provides an automated tool to characterize engineered tissue fiber network topology is presented. Micro-architectural features that fully defined fiber network topology were detected and quantified, which include fiber orientation, connectivity, intersection spatial density, and diameter. Algorithm performance was tested using scanning electron microscopy (SEM) images of electrospun poly(ester urethane)urea (ES-PEUU) scaffo…

ScaffoldMaterials sciencePolyestersPolyurethanesBiophysicsBioengineeringTopology (electrical circuits)TopologyCell morphologyArticleBiomaterialsTissue engineeringMicroscopyAnimalsHumansFiberDecellularizationTissue EngineeringTissue ScaffoldsPhantoms ImagingMesenchymal Stem CellsElectrospinningRatsMechanics of MaterialsMicroscopy Electron ScanningCeramics and CompositesCollagenRabbitsGelsAlgorithmsBiomedical engineeringImage analysisScaffold morphologyMicrostructureElectrospinningCollagen gelDecellularized tissue
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Morphostructural analysis of human follicular stem cells on highly porous bone hydroxyapatite scaffold

2007

In this study we investigated the in vitro behaviour, morphostructure and extracellular matrix synthesis of human dental follicular stem cells (hDFSCs) isolated from human dental bud, which resulted to be positive for mesenchymal markers (CD29, CD90, CD146 and CD166) by FACS analysis. Cells were analysed by light and electronic microscopy to evaluate their biological response either at week 1, that is before differentiation, or at weeks 3–6, when they had been cultured in osteogenic medium onto a highly porous natural scaffold material (Bio-Oss®). Microscopy analysis of primary culture cells showed they had a mesenchymal stem cell-like morphostructure, spindle shaped, similar to the cultur…

Scaffolddental fiollicle stem cells tissue engineering porous bone hydroxyapatite (Bio-Oss (R))ImmunologyDentistryBiocompatible MaterialsExtracellular matrix03 medical and health sciencesdental fiollicle0302 clinical medicineTissue engineeringHighly porousFollicular phaseHumansImmunology and AllergyCells CulturedPharmacologyDental follicleTissue EngineeringTissue Scaffoldsbusiness.industryChemistryStem CellsCell DifferentiationFibroblastsFlow CytometryIn vitroExtracellular MatrixCell biologyDurapatitePhenotypeporous bone hydroxyapatite (Bio-Oss (R))030220 oncology & carcinogenesisMicroscopy Electron ScanningStem cellbusinessPorosityTooth030215 immunology
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FACS-based protocol to assess cytotoxicity and clonogenic potential of colorectal cancer stem cells using a Wnt/β-catenin signaling pathway reporter

2021

Summary Cancer stem cells (CSCs) play a key role in tumor initiation and progression. A real-time tool to evaluate the activation of CSC-specific signaling pathways is crucial for the study of this cancer cell subset. Here, we present a protocol to monitor, in vitro, the activation of Wnt/β-catenin signaling pathway, which is considered a functional biomarker for colorectal CSCs (CR-CSCs). This flow-cytometry-based protocol allows it to isolate CR-CSCs and to evaluate their cytotoxicity upon anti-tumor treatments. For complete details on the use and execution of this protocol, please refer to Di Franco et al. (2021).

Science (General)Colorectal cancerTumor initiationBiologyGeneral Biochemistry Genetics and Molecular BiologyQ1-390Cancer stem cellmedicineProtocolHumansFlow Cytometry/Mass CytometryClonogenic assayWnt Signaling PathwayCancerGeneral Immunology and MicrobiologyGeneral NeuroscienceStem CellsWnt signaling pathwayCancerCell Biologymedicine.diseaseFlow CytometryMolecular/Chemical ProbesCancer cellcolorectal cancers cancer stem cells FACS Wnt.Cell isolationCancer researchNeoplastic Stem CellsCell-based AssaysStem cellSettore MED/46 - Scienze Tecniche Di Medicina Di LaboratorioColorectal NeoplasmsSignal TransductionSTAR Protocols
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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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Regulation of the p19(Arf)/p53 pathway by histone acetylation underlies neural stem cell behavior in senescence-prone SAMP8 mice.

2015

Brain aging is associated with increased neurodegeneration and reduced neurogenesis. B1/neural stem cells (B1-NSCs) of the mouse subependymal zone (SEZ) support the ongoing production of olfactory bulb interneurons, but their neurogenic potential is progressively reduced as mice age. Although age-related changes in B1-NSCs may result from increased expression of tumor suppressor proteins, accumulation of DNA damage, metabolic alterations, and microenvironmental or systemic changes, the ultimate causes remain unclear. Senescence-accelerated-prone mice (SAMP8) relative to senescence-accelerated-resistant mice (SAMR1) exhibit signs of hastened senescence and can be used as a model for the stud…

SenescenceMaleAgingHistonesMiceNeural Stem CellsNeurospheremedicineSubependymal zoneAnimalsstem cell nicheCyclin-Dependent Kinase Inhibitor p19Mice KnockoutNeuronsbiologyNeurodegenerationNeurogenesishistone acetyltransferasesBrainAcetylationCell BiologyOriginal Articlesmedicine.diseaseGenes p53Neural stem cellChromatinCell biologyadult neurogenesisOxidative StressHistoneImmunologybiology.proteinProtein Processing Post-TranslationalSAMP8 micehistone deacetylasesAging cell
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The importance of culturing primary cells under physiological conditions: proliferation, senescence, pluripotency

2017

Mesenchymal stem cells (MSCs), such as human dental pulp stem cells (hDPSCs), are currently a source for cell therapy. However, cell therapy protocols require 10–400 million cells per treatment, and consequently, they need to be expanded in vitro before implantation, with the inconvenience that MSCs undergo senescence following a certain number of cell expansion passages, loosing their stem cell qualities. Ambient oxygen tension (21% pO2) is normally used for in vitro culture, but physiological levels in vivo range between 3% and 6% pO2. We previously demonstrated that hDPSC proliferation rate is significantly lowered at 21% pO2 due to enhanced oxidative stress, which led to the activation …

SenescenceMesenchymal stem cellBiologymedicine.disease_causeBiochemistryCell biologyCell therapySOX2KLF4Physiology (medical)Dental pulp stem cellsmedicineStem cellOxidative stressFree Radical Biology and Medicine
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