Search results for "Flow Cytometry"

showing 10 items of 814 documents

Radiobiological characterization of human tumor cell multilayers after conventional and particle irradiation.

2006

The goal of this study was to establish planar multilayers from human tumor cells (WiDr and SiHa) as a model for irradiation of solid tumors. In addition to using conventional X rays (250 kV) as a reference standard, multilayers were tested for their suitability in cell survival studies with heavy-ion irradiation ((12)C(6+)) in the plateau and the extended Bragg peak with a scanned ion beam. Multilayers of both cell lines showed decreased survival compared to the corresponding monolayers after both X and heavy-ion irradiation. This multicellular sensitization effect is in contrast to the multicellular resistance or contact effect commonly described in the literature. Flow cytometry measurem…

Materials scienceIon beamCell SurvivalCellBiophysicsNanotechnologyBragg peakHeavy Ion RadiotherapyX-Ray TherapyRadiation DosageFlow cytometryCell Line TumorSpheroids CellularMonolayermedicineHumansRadiology Nuclear Medicine and imagingIrradiationRadiationmedicine.diagnostic_testRadiobiologyDose-Response Relationship RadiationHuman tumormedicine.anatomical_structureTreatment OutcomeCell cultureBiophysicsRadiation research
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Characterization of a new murine retinal cell line (MU-PH1) with glial, progenitor and photoreceptor characteristics

2013

Unlike fish and amphibians, mammals do not regenerate retinal neurons throughout life. However, neurogenic potential may be conserved in adult mammal retina and it is necessary to identify the factors that regulate retinal progenitor cells (RPC) proliferative capacity to scope their therapeutic potential. Müller cells can be progenitors for retinal neuronal cells and can play an essential role in the restoration of visual function after retinal injury. Some members of the Toll-like receptor (TLR) family, TLR2, TLR3 and TLR4, are related to progenitor cells proliferation. Müller cells are important in retinal regeneration and stable cell lines are useful for the study of retinal stem cell bi…

MelanopsinPhotoreceptorsOpsinFarmacologíaBlotting WesternBiologyMüllerBiología CelularFisiologíaProgenitor cellsRetinaCell LineCellular and Molecular Neurosciencechemistry.chemical_compoundMiceRecoverinmedicineAnimalsTLR2Photoreceptor CellsProgenitor cellEye ProteinsRetinal regenerationCell ProliferationFluorescent DyesRetinaAniline CompoundsCell growthReverse Transcriptase Polymerase Chain ReactionTumor Necrosis Factor-alphaStem CellsRetinalFlow CytometrySensory SystemsCell biologyMice Inbred C57BLOphthalmologymedicine.anatomical_structurechemistryXanthenesbiology.proteinCalciumFemalesense organsNeuroscienceNeurogliaBiomarkers
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Flow cytometry, sorting and immunocharacterization with proliferating cell nuclear antigen of cycling and non-cycling cells in synchronized pea root …

1997

In the 3-d-old 2-mm root tip of Pisum sativum L. cv. Lincoln the percentage of actively proliferating cells is estimated to be 70%. The remaining cells are non-cycling and arrested with 2C and 4C DNA content in G0 and in G2Q, respectively. In this work we studied the kinetic significance of these quiescent cells, using the sorting capabilities of flow cytometry and immunofluorescence techniques to detect the proliferation marker PCNA (proliferating cell nuclear antigen) inside cells within the different cell-cycle compartments. While in animal cells, PCNA is present at a high level only in actively proliferating cells, in 3-d-old pea root tips 95% of the cells are PCNA-positive. After flow …

MeristemPlant ScienceBiologyImmunofluorescencePlant RootsPisumFlow cytometryProliferating Cell Nuclear AntigenGeneticsmedicineHydroxyureaProliferation MarkerFluorescent Antibody Technique IndirectRoot capCell Nucleusmedicine.diagnostic_testCell CyclePeasMicrotomyCell cycleMeristemFlow Cytometrybiology.organism_classificationProliferating cell nuclear antigenCell biologybiology.proteinPlanta
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Influence of cell-cell contact between L. thermotolerans and S. cerevisiae on yeast interactions and the exo-metabolome

2019

International audience; Sequential fermentation of grape must inoculated with L. thermotolerans and then S. cerevisiae 24 h later (typical wine-making practice) was conducted with or without cell-cell contact between the two yeast species. We monitored cell viability of the two species throughout fermentation by flow cytometry. The cell viability of S. cerevisiae decreased under both conditions, but the decrease was greater if there was cell-cell contact. An investigation of the nature of the interactions showed competition between the two species for nitrogen compounds, oxygen, and must sterols. Volatile-compound analysis showed differences between sequential and pure fermentation and that…

MetaboliteL. thermotoleransInteractionsS. cerevisiaeWineSaccharomyces cerevisiaeMicrobiologyFlow cytometry03 medical and health scienceschemistry.chemical_compoundMetabolomicsMetabolomemedicineMetabolomics[CHIM]Chemical SciencesVitisViability assayFlow cytometryCell-cell contact030304 developmental biology0303 health sciencesCell cell contactMicrobial Viabilitymedicine.diagnostic_testEthanol030306 microbiologyChemistryfood and beveragesYeastCoculture TechniquesOxygenBiochemistryInteractions ; S. Cerevisiae ; L. Thermotolerans ; Cell-cell Contact ; Flow Cytometry ; MetabolomicsFermentationSaccharomycetalesMetabolomeMicrobial InteractionsFermentationFood Science
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Flow cytometric analysis of peroxidative activity in granulocytes from coronary and peripheral blood in acute myocardial ischemia and reperfusion in …

1999

BACKGROUND Methionine has shown protective effects in experimental models of myocardial infarction and is highly reactive to oxidative compounds produced by polymorphonuclear leukocytes (PMN), which in turn have been associated with myocardial damage. We have investigated the effect of methionine administration on spontaneous leukocyte peroxidative activity in myocardial ischemia and reperfusion. METHODS In anesthetized dogs, with coronary occlusion (90 min) and reperfusion (90 min), PMN activation was measured by flow cytometric determination of H(2)O(2) with dihydrorhodamine 123, and correlated to hemodynamic parameters and infarct presence. To assess a possible direct effect of methionin…

Methioninemedicine.diagnostic_testChemistrySuperoxideBiophysicsHemodynamicsCell BiologyHematologyVenous bloodOxidative phosphorylationPharmacologyPathology and Forensic MedicineFlow cytometrychemistry.chemical_compoundEndocrinologyIn vivoCoronary occlusionmedicineCytometry
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Apoptosis in malignant glioma cells triggered by the temozolomide-induced DNA lesion O6-methylguanine

2006

Methylating drugs such as temozolomide (TMZ) are widely used in the treatment of brain tumours (malignant gliomas). The mechanism of TMZ-induced glioma cell death is unknown. Here, we show that malignant glioma cells undergo apoptosis following treatment with the methylating agents N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) and TMZ. Cell death determined by colony formation and apoptosis following methylation is greatly stimulated by p53. Transfection experiments with O(6)-methylguanine-DNA methyltransferase (MGMT) and depletion of MGMT by O(6)-benzylguanine showed that, in gliomas, the apoptotic signal originates from O(6)-methylguanine (O(6)MeG) and that repair of O(6)MeG by MGMT prevent…

MethylnitronitrosoguanidineCancer ResearchProgrammed cell deathFas Ligand ProteinGuanineDNA repairFas-Associated Death Domain ProteinBlotting WesternApoptosisBiologymedicine.disease_causeO(6)-Methylguanine-DNA MethyltransferaseGliomaTemozolomideTumor Cells CulturedGeneticsmedicineHumansDNA Breaks Double-StrandedRNA Small InterferingAntineoplastic Agents AlkylatingneoplasmsMolecular BiologyTumor Stem Cell AssayCell ProliferationTemozolomideBrain NeoplasmsCell CycleGliomaCell cycleFlow CytometryFas receptormedicine.diseaseDacarbazineProto-Oncogene Proteins c-bcl-2ApoptosisCaspasesCancer researchTumor Suppressor Protein p53CarcinogenesisDNA Damagemedicine.drugOncogene
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Hepatocytes of double-transgenic mice expressing high levels of hepatitis B virus e antigen and interferon-gamma are not injured by HBeAg specific au…

2000

Seroconversion from HBeAg to alphaHBe of persons chronically infected by HBV is usually associated with a transient exacerbation of liver disease and subsequent normalization of liver histology. It is speculated that these clinico-pathological features may be due to the activation of cytodestructive mechanisms by alphaHBe antibodies. The aim of the present study was to investigate the pathogenic potential of alphaHBe antibodies in a transgenic mouse model. Therefore, alphaHBe autoantibodies were elicited in double-transgenic mice expressing high amounts of HBeAg and interferon-gamma in the liver. Interferon-gamma has reviously been shown to play an important role in the development of hepat…

Mice Transgenicmedicine.disease_causeTransfectionCell LineLiver diseaseInterferon-gammaMiceInterferonAntibody SpecificityVirologymedicineAnimalsInterferon gammaHepatitis B e AntigensSeroconversionHepatitis B AntibodiesProtein PrecursorsAutoantibodiesHepatitis B virusbiologyViral Core Proteinsvirus diseasesInterferon-alphaGeneral Medicinemedicine.diseasebiology.organism_classificationFlow CytometryHepatitis BVirologydigestive system diseasesHepadnaviridaeHBeAgLiverImmunologybiology.proteinAntibodymedicine.drugArchives of virology
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Performance of the QuantiFERON-cytomegalovirus (CMV) assay for detection and estimation of the magnitude and functionality of the CMV-specific gamma …

2012

ABSTRACTThe performance of the QuantiFERON-cytomegalovirus (CMV) assay was compared to that of a flow cytometry intracellular cytokine staining (ICS) method for the detection of CMV-specific gamma interferon (IFN-γ)-producing CD8+T-cell responses in allogeneic stem cell transplant (allo-SCT) recipients and for estimations of their magnitude and functionality. A total of 90 whole-blood specimens from 23 allo-SCT recipients was analyzed by both methods. Overall, the percentage of specimens that yielded concordant results by both methods was 68.8% (κ = 0.691; 95% confidence interval [CI], 0.548 to 0.835), and the sensitivity of the QuantiFERON-CMV assay for the detection of positive IFN-γ T-ce…

Microbiology (medical)AdultMaleClinical BiochemistryImmunologyCongenital cytomegalovirus infectionCytomegalovirusBiologyCD8-Positive T-LymphocytesSensitivity and SpecificityFlow cytometryQuantiFERONGamma interferonDiagnostic Laboratory ImmunologymedicineImmunology and AllergyCytotoxic T cellHumansAgedTransplantationmedicine.diagnostic_testMiddle Agedmedicine.diseaseConfidence intervalImmunologyCytomegalovirus InfectionsFemaleStem cellCD8Interferon-gamma Release TestsStem Cell TransplantationClinical and vaccine immunology : CVI
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Selective growth-inhibitory effect of 8-hydroxyquinoline towards Clostridium difficile and Bifidobacterium longum subsp. longum in co-culture analyse…

2014

The major risk factor for Clostridium difficile infection (CDI) is the use of antibiotics owing to the disruption of the equilibrium of the host gut microbiota. To preserve the beneficial resident probiotic bacteria during infection treatment, the use of molecules with selective antibacterial activity enhances the efficacy by selectively removing C. difficile. One of them is the plant alkaloid 8-hydroxyquinoline (8HQ), which has been shown to selectively inhibit clostridia without repressing bifidobacteria. Selective antimicrobial activity is generally tested by culture techniques of individual bacterial strains. However, the main limitation of these techniques is the inability to describe …

Microbiology (medical)Bifidobacterium longumbiologymedicine.diagnostic_testClostridioides difficilemedicine.drug_classAntibioticsGeneral MedicineClostridium difficileGut floraFlow CytometryOxyquinolinebiology.organism_classificationAntimicrobialMicrobiologyAnti-Bacterial AgentsFlow cytometryMicrobiologyClostridiamedicineMicrobial InteractionsBifidobacteriumAntibacterial activityIn Situ Hybridization FluorescenceJournal of Medical Microbiology
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Improved assessment of T-cell receptor (TCR) VB repertoire in clinical specimens: combination of TCR-CDR3 spectratyping with flow cytometry-based TCR…

2002

ABSTRACTAntigen-specific T-cell responses may be described by combining three categories: (i) the specificity and effector functions of a T-cell population, (ii) the quantity of T-cell responses (i.e., the number of responding T cells within the CD4/CD8 population), and (iii) the “quality” of T cells (defined by the T-cell receptor [TCR] structure). Several methods to measure T-cell responses are now available including evaluation of T-cell precursors using limiting dilution, the enzyme-linked immunospot assay, ex vivo TCR variable (v)-segment analysis determined by flow cytometry, and TCR-CDR3 length analysis (spectratyping), as well as identification of peptide-specific T cells using majo…

Microbiology (medical)CD4-Positive T-LymphocytesReceptors Antigen T-Cell alpha-betaClinical BiochemistryImmunologyPopulationchemical and pharmacologic phenomenaComplementarity determining regionCD8-Positive T-LymphocytesMajor histocompatibility complexCDR3 SpectratypingFlow cytometryNeoplasmsCellular ImmunologymedicineImmunology and AllergyHumanseducationeducation.field_of_studybiologymedicine.diagnostic_testT-cell receptorhemic and immune systemsFlow CytometryMolecular biologyComplementarity Determining RegionsImmunologybiology.proteinAntibodyCD8Clinical and diagnostic laboratory immunology
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