Search results for "differentiation"

showing 10 items of 1605 documents

The influence of bone allograft processing on osteoblast attachment and function

2004

In order to assess the influence of eight different sterilisation and disinfection methods for bone allografts on adhesion, proliferation, and differentiation of human bone marrow stromal cells (BMSC), cells were grown in culture and then plated onto pieces of human bone allografts. Following processing methods were tested: autoclavation (AUT), low-temperature-plasma sterilisation of demineralised allografts (D-LTP), ethylene oxide sterilisation (EtO), fresh frozen bone (FFB), 80 degrees C-thermodisinfection (80 degrees C), gamma-irradiation (Gamma), chemical solvent disinfection (CSD), and Barrycidal-disinfection (BAR). The seeding efficiency was determined after one hour to detect the num…

Stromal cellCell Survivalmedicine.medical_treatmentOsteocalcinPopulationGene ExpressionBone Marrow CellsIn Vitro TechniquesBone graftingAndrologyCell AdhesionmedicineHumansTransplantation HomologousOrthopedics and Sports MedicineViability assayCell adhesioneducationCells CulturedBone Marrow Transplantationeducation.field_of_studyOsteoblastsbiologyChemistrySterilizationCell DifferentiationOsteoblastAlkaline PhosphataseTransplantationmedicine.anatomical_structureImmunologyOsteocalcinbiology.proteinStromal CellsCell DivisionJournal of Orthopaedic Research
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Novel Immunomodulatory Markers Expressed by Human WJ-MSC: an Updated Review in Regenerative and Reparative Medicine.

2012

Mesenchymal (stromal) stem cells (MSC) are a broad class of stromal populations which are able to differentiate towards mature cell types, and do express molecules involved in immune modulation, tolerance induction and inflammation dampening. MSC can be virtually isolated from each adult organ, as well as from foetus-associated perinatal tissues. In particular, Wharton's jelly-derived MSC (WJ-MSC) bear all of these key properties, together with their ease of sourcing and lack of ethical issues. Cellular therapy is a key technique in regenerative medicine approaches, in particular for the treatment of diseases in which physiological processes of cellular repopulation are blocked by the under…

Stromal cellCellular differentiationImmune modulationRegenerative medicineCell therapyDevelopmental NeuroscienceMedicineProgenitor cellTissue repairUmbilical cordMesenchymal stem cellInflammationbusiness.industrySettore BIO/16 - Anatomia UmanaWharton's jellyMesenchymal stem cellMatrix metalloproteinaseTolerance inductionDifferentiationHypoimmunogenicityImmunologyRegenerative medicineStem cellbusinessNeuroscienceDevelopmental Biology
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Efficient differentiation of embryonic stem cells into mesodermal precursors by BMP, retinoic acid and Notch signalling

2012

The ability to direct differentiation of mouse embryonic stem (ES) cells into specific lineages not only provides new insights into the pathways that regulate lineage selection but also has translational applications, for example in drug discovery. We set out to develop a method of differentiating ES cells into mesodermal cells at high efficiency without first having to induce embryoid body formation. ES cells were plated on a feeder layer of PA6 cells, which have membrane-associated stromal-derived inducing activity (SDIA), the molecular basis of which is currently unknown. Stimulation of ES/PA6 co-cultures with Bone Morphogenetic Protein 4 (BMP4) both favoured self-renewal of ES cells and…

Stromal cellCellular differentiationMyocytes Smooth MuscleNotch signaling pathwaylcsh:MedicineDevelopmental SignalingTretinoinEmbryoid bodyBiologyCell LineMesoderm03 medical and health sciencesMice0302 clinical medicineRetinoic Acid Signaling CascadeMolecular Cell BiologyExpressió genèticaAnimalslcsh:ScienceBiologyEmbryonic Stem Cells030304 developmental biology0303 health sciencesMultidisciplinaryReceptors NotchStem Cellslcsh:RComputational BiologyCell DifferentiationNestinSignaling in Selected DisciplinesMolecular biologyEmbryonic stem cellSignaling CascadesSignaling NetworksP19 cellBone morphogenetic protein 4embryonic structuresBone Morphogenetic Proteinslcsh:QCellular TypesStromal CellsTranscriptomeCèl·lules mare030217 neurology & neurosurgeryResearch ArticleDevelopmental BiologySignal Transduction
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Biomaterials coated by dental pulp cells as substrate for neural stem cell differentiation

2011

[EN] This study is focused on the development of an in vitro hybrid system, consisting in a polymeric biomaterial covered by a dental pulp cellular stroma that acts as a scaffold offering a neurotrophic support for the subsequent survival and differentiation of neural stem Cells. In the first place, the behavior of dental pulp stroma on the polymeric biomaterial based on ethyl acrylate and hydroxy ethyl acrylate copolymer was studied. For this purpose, cells from normal human third molars were grown onto 0.5-mm-diameter biomaterial discs. After cell culture, quantification of neurotrophic factors generated by the stromal cells was performed by means of an ELISA assay. In the second place, s…

Stromal cellMaterials scienceBiomedical EngineeringBiomaterialsCell therapyMiceNerve growth factorCoated Materials BiocompatibleNeural Stem Cellsstomatognathic systemNeurotrophic factorsAnimalsHumansNeural cellCells CulturedDental PulpCell ProliferationNeuronsStem cellBrain-Derived Neurotrophic FactorMetals and AlloysBiomaterialCell adhesionCell DifferentiationNeural stem cellRatsCell biologystomatognathic diseasesCell cultureMAQUINAS Y MOTORES TERMICOSCeramics and CompositesCell cultureStem cellNeural cellBiomedical engineering
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The Influence of Cultivation Conditions on the Proliferation and Differentiation of Rat Bone Marrow Multipotent Mesenchymal Stromal Cells

2008

Rat bone marrow multipotent mesenchymal stromal cells (rBM MMSCs) demonstrate a potential to differentiate down the mesodermal pathway but under appropriate experimental condition differentiation into non-mesodermal lineages may occur. Knowing this fact it seems interesting whether prolonged cultivation and preservation affects BM MMSC morphology, differentiation ability into multiple lineages and proliferation capacity. Therefore this study was aimed to investigate the effects of long-term cultivation and cryopreservation on the morphology, proliferation and differentiation potential of rat bone marrow-derived MMSCs in vitro.

Stromal cellTransdifferentiationMultipotent Mesenchymal Stromal CellsBiologyRat Bone MarrowIn vitroCryopreservationCell biology
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Spatial analysis of plant metabolism: Sucrose imaging within Vicia faba cotyledons reveals specific developmental patterns

2002

During legume embryogenesis the differentiation of the cotyledons proceeds gradually in a wave-like manner. The process is metabolically and genetically controlled and regulated by sugars. In order to perform a spatial and temporal analysis of the sugar distribution pattern a new method was developed to specifically measure sucrose directly in tissues via bioluminescence and single photon counting. This enabled a quantitative sucrose imaging with a resolution close to the single cell level. The procedure was applied on sections of Vicia faba cotyledons covering the main stages of histodifferentiation. Young embryos before the storage phase contained moderate levels of sucrose, which were ev…

SucroseSucrosefood.ingredientLightStarchGlucose-1-Phosphate AdenylyltransferasePlant ScienceBiologyCarbohydrate metabolismPlant Epidermischemistry.chemical_compoundfoodGeneticsSugarCell SizePlant ProteinsMembrane Transport Proteinsfood and beveragesCell DifferentiationFabaceaeStarchCell BiologyCarbohydrateNucleotidyltransferasesVicia fabachemistryBiochemistryGlucosyltransferasesLuminescent MeasurementsSeedsbiology.proteinCarbohydrate MetabolismSucrose synthaseCotyledonSignal TransductionThe Plant Journal
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Dependency of the in vitro stabilization of differentiated functions in liver parenchymal cells on the type of cell line used for co-culture.

1992

The differentiation status in cultures of primary rat liver parenchymal cells was determined by measuring the activities of various xenobiotic metabolizing enzymes. Most enzyme activities dropped rather rapidly in monocultures of parenchymal cells. The protein content and the activities of cytosolic epoxide hydrolase, glutathione S-transferase, and alpha-naphthol UDP-glucuronosyl transferase were, however, well stabilized in 7-day-old co-cultures of parenchymal cells with two different lines of rat liver nonparenchymal epithelial cells (NEC1 and NEC2). Phenol sulfotransferase and microsomal epoxide hydrolase activity were reduced in this coculture system after 7 days to about 30 and 20% of …

SulfotransferaseClinical BiochemistryBiologyCell LineXenobioticschemistry.chemical_compoundmedicineAnimalsGlutathione transferase activityGlucuronosyltransferaseEpoxide hydrolaseCells CulturedGlutathione TransferaseEpoxide HydrolasesProteinsCell DifferentiationCell BiologyGeneral MedicineGlutathioneArylsulfotransferaseRatsmedicine.anatomical_structurechemistryBiochemistryLiverCell cultureMicrosomal epoxide hydrolaseHepatocyteStem cellDevelopmental BiologyIn vitro cellulardevelopmental biology : journal of the Tissue Culture Association
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The role of NF-AT transcription factors in T cell activation and differentiation11We dedicate this review to Prof. Dr. Rigomar Rieger (Gatersleben), …

2000

AbstractThe family of genuine NF-AT transcription factors consists of four members (NF-AT1 [or NF-ATp], NF-AT2 [or NF-ATc], NF-AT3 and NF-AT4 [or NF-ATx]) which are characterized by a highly conserved DNA binding domain (is designated as Rel similarity domain) and a calcineurin binding domain. The binding of the Ca2+-dependent phosphatase calcineurin to this region controls the nuclear import and exit of NF-ATs. This review deals (1) with the structure of NF-AT proteins, (2) the DNA binding of NF-AT factors and their interaction with AP-1, (3) NF-AT target genes, (4) signalling pathways leading to NF-AT activation: the role of protein kinases and calcineurin, (5) the nuclear entry and exit …

T cell activationCellular differentiationT cell differentiationCell BiologyDNA-binding domainCell cycleBiologyInterleukinNFATC Transcription FactorsAP-1Molecular biologyCalcineurinCyclosporin AT cell differentiationNF-AT transcription factorNuclear proteinMolecular BiologyTranscription factorBiochimica et Biophysica Acta (BBA) - Molecular Cell Research
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Neuronal nitric oxide synthase modulates maturation of human dendritic cells.

2010

AbstractDendritic cells (DCs) are the most potent APCs of the immune system. Understanding the intercellular and intracellular signaling processes that lead to DC maturation is critical for determining how these cells initiate T cell-mediated immune processes. NO synthesized by the inducible NO synthase (iNOS) is important for the function of murine DCs. In our study, we investigated the regulation of the arginine/NO-system in human monocyte-derived DCs. Maturation of DCs induced by inflammatory cytokines (IL-1β, TNF, IL-6, and PGE2) resulted in a pronounced expression of neuronal NOS (nNOS) but only minimal levels of iNOS and endothelial NOS were detected in human mature DCs. In addition, …

T cellCellular differentiationImmunologyImmunoblottingchemical and pharmacologic phenomenaEnzyme-Linked Immunosorbent AssayCell SeparationNitric Oxide Synthase Type IBiologyEndothelial NOSLymphocyte ActivationNitric OxideProinflammatory cytokineCell LineImmune systemmedicineImmunology and AllergyHumansAutocrine signallingMHC class IIReverse Transcriptase Polymerase Chain ReactionCell DifferentiationDendritic CellsFlow CytometryCell biologymedicine.anatomical_structureCell culturebiology.proteinCytokinesJournal of immunology (Baltimore, Md. : 1950)
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Induction of tumor peptide-specific cytotoxic T cells under serum-free conditions by mature human dendritic cells

2000

Tumor vaccination strategies using antigen-pulsed dendritic cells (DC) are currently under development. We established an in vitro system using cultured DC from HLA-typed volunteers for the induction of tumor peptide-specific CD8+ T cells. The strength and specificity of the resulting CTL responses were investigated. For stimulation of syngeneic CD8+ T cells two well-defined DC populations were generated: CD1a+ immature DC cultured in the presence of GM-CSF and IL-4 and mature CD83+ DC generated by additional stimulation with a cytokine cocktail. Stimulations were performed under serum-free conditions and in the absence of exogenous cytokines. Analysis of T cell responses showed that mature…

T cellImmunoglobulinsPriming (immunology)DermatologyDendritic cell differentiationCD8-Positive T-LymphocytesBiologyCulture Media Serum-FreeInterleukin 21Antigens CDmedicineHumansCytotoxic T cellCells CulturedCellular SenescenceMembrane GlycoproteinsCell DifferentiationDendritic CellsGeneral MedicineDendritic cellMolecular biologyNeoplasm ProteinsDrug CombinationsCTL*medicine.anatomical_structureImmunologyCytokinesCD8T-Lymphocytes Cytotoxic
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