Search results for "Cytometry"

showing 10 items of 852 documents

Direct Toll-Like Receptor-Mediated Stimulation of Hematopoietic Stem and Progenitor Cells Occurs In Vivo and Promotes Differentiation Toward Macropha…

2012

Abstract As Toll-like receptors (TLRs) are expressed by hematopoietic stem and progenitor cells (HSPCs), they may play a role in hematopoiesis in response to pathogens during infection. We show here that TLR2, TLR4, and TLR9 agonists (tripalmitoyl-S-glyceryl-L-Cys-Ser-(Lys)4 [Pam3CSK4], lipopolysaccharide [LPS], and CpG oligodeoxynucleotide [ODN]) induce the in vitro differentiation of purified murine lineage negative cells (Lin−) as well as HSPCs (identified as Lin− c-Kit+ Sca-1+ IL-7Rα− [LKS] cells) toward macrophages (Mph), through a myeloid differentiation factor 88 (MyD88)-dependent pathway. In order to investigate the possible direct interaction of soluble microorganism-associated mol…

Hematopoietic stem and progenitor cellsBiologyCell LineMicemedicineAnimalsProgenitor cellToll-like receptorInnate immune systemMacrophagesToll-Like ReceptorsTLR9Cell DifferentiationCell BiologyFlow CytometryHematopoietic Stem CellsMyD88Molecular biologyToll-Like Receptor 2Toll-like receptorsMice Inbred C57BLToll-Like Receptor 4TLR2Haematopoiesismedicine.anatomical_structureMyeloid Differentiation Factor 88TLR4Molecular MedicineBone marrowDevelopmental BiologySignal Transduction
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Molecular analysis on the chemopreventive properties of resveratrol, a plant polyphenol microcomponent.

2002

As a plant microcomponent, resveratrol is a polyphenolic compound produced by several species and found especially in Polygonum roots, peanuts seeds, berries and also grape and therefore can be present in human diet or beverages (red wine, for instance). Traditional chinese medicine and more recent epidemiological studies strongly suggested that resveratrol may act as a cancer chemopreventive compound. The biochemical mechanism by which resveratrol inhibits cell proliferation was provided by studies in numerous human cell lines including our work in hepatoblastoma HepG2 and colorectal tumor SW480 cells. The results show that resveratrol strongly inhibits cell proliferation at the micromolar…

HepatoblastomaCellGenisteinResveratrolBiologyIn Vitro Techniqueslaw.inventionS Phasechemistry.chemical_compoundlawNeoplasmsStilbenesGeneticsmedicineTumor Cells CulturedHumansCell growthfood and beveragesGeneral MedicineCell cycleFlow CytometryAntineoplastic Agents PhytogenicGenisteinmedicine.anatomical_structurechemistryBiochemistryApoptosisPolyphenolResveratrolColonic NeoplasmsPhytotherapyCell DivisionInternational journal of molecular medicine
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Specific Identification and Quantification of the Spoilage Microorganism Brettanomyces in Wine by Flow Cytometry: A Useful Tool for Winemakers

2010

International audience; no abstract

HistologyBrettanomycesMicroorganismFood spoilageBrettanomycesWine[ CHIM ] Chemical SciencesPathology and Forensic MedicineFlow cytometry03 medical and health sciencesmedicine[CHIM]Chemical SciencesFood scienceIn Situ HybridizationComputingMilieux_MISCELLANEOUS030304 developmental biologyWine0303 health sciencesmedicine.diagnostic_testbiology030306 microbiologyChemistryCell BiologyFlow Cytometrybiology.organism_classificationFermentationFermentationSpecific identification
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Effects of caspase inhibitors (z-VAD-fmk, z-VDVAD-fmk) on Nile Red fluorescence pattern in 7-ketocholesterol-treated cells: Investigation by flow cyt…

2007

Background: The 7-ketocholesterol (7KC)-induced cell death has some characteristics of apoptosis and is associated with polar lipid accumulation. So, we investigated the effects of the broad-spectrum caspase inhibitor z-VAD-fmk and of the caspase-2 inhibitor z-VDVAD-fmk on lipid profile evaluated by staining with Nile Red (NR). Methods: The 7KC-treated human monocytic U937 cells were cultured in the absence or in the presence of the caspase inhibitors z-VAD-fmk or z-VDVAD-fmk. When staining with NR is performed, neutral and polar lipids have yellow and orange/red emission, respectively, and fluorescence was then analyzed by flow cytometry (FCM) and by confocal laser scanning microscopy (CLS…

HistologyConfocalCaspase 2FluorescencePathology and Forensic Medicinelaw.inventionFlow cytometryAmino Acid Chloromethyl Ketones03 medical and health scienceschemistry.chemical_compound0302 clinical medicineConfocal microscopylawOxazinesmedicineImage Processing Computer-AssistedHumans[ SDV.IB ] Life Sciences [q-bio]/BioengineeringEnzyme InhibitorsKetocholesterols030304 developmental biology[SDV.IB] Life Sciences [q-bio]/BioengineeringCell Nucleus0303 health sciencesMicroscopyMicroscopy Confocalbiologymedicine.diagnostic_testNile redLipid metabolismCell BiologyU937 CellsFlow CytometryLipid MetabolismFluorescenceMolecular biologyCaspase Inhibitors3. Good healthStainingchemistry030220 oncology & carcinogenesisbiology.protein[SDV.IB]Life Sciences [q-bio]/Bioengineeringbiological phenomena cell phenomena and immunityFactor Analysis Statistical
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Functional assays of oxidative stress using genetically engineered Escherichia coli strains.

2003

Oxidative stress may be induced in bacteria by exogenous biocidal agents and is involved in endogenous metabolism. The oxyR operon is a main sensor of oxidative stress and oxyR-deficient bacteria show enhanced sensitivity to oxidative stress and increased accumulation of intracellular reactive oxygen species (ROS). Flow cytometric functional assays in bacteria are limited by the impaired penetration of vital dyes trough the cell wall. Escherichia coli B WP2 strains possess an altered cell-wall lipopolysaccharide that leads to increased membrane permeability. Flow cytometric analysis of WP2 strains is a convenient alternative for cytometric assays of bacterial function. This unit presents pr…

HistologyMembrane permeabilityLipopolysaccharideOperonBiologymedicine.disease_causeBiochemistryCell wallchemistry.chemical_compoundmedicineEscherichia coliEscherichia coliFluorescent DyesEscherichia coli ProteinsGeneral Medicinebiology.organism_classificationFlow CytometryDNA-Binding ProteinsRepressor ProteinsMedical Laboratory TechnologyOxidative StressBiochemistrychemistrybacteriaGenetic EngineeringReactive Oxygen SpeciesIntracellularBacteriaOxidative stressCurrent protocols in cytometry
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Estimation of Microbial Viability Using Flow Cytometry.

2020

For microorganisms in particular, viability is a term that is difficult to define and a state consequently difficult to measure. The traditional (and gold standard) usage equates viability and culturability (i.e., the ability to multiply) but the process of determining culturability is often too slow. Flow cytometry provides the opportunity to make rapid and quantitative measurements of dye uptake in large numbers of cells and we can therefore exploit the flow cytometric approach to evaluate so-called viability stains and to develop protocols for more routine assessments of microbial viability. This article provides a commentary and several protocols have been included to ensure that users …

HistologyMicrobial ViabilityMicrobial Viabilitymedicine.diagnostic_testStaining and LabelingComputer scienceGeneral MedicineFlow CytometryFluoresceinsBiochemistryFluorescenceFlow cytometryMedical Laboratory TechnologyDye uptakeCalibrationmedicineBiochemical engineeringFluorescent DyesCurrent protocols in cytometryLITERATURE CITED
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Sequence of lethal events in HeLa cells exposed to the G2 blocking cytolethal distending toxin

2000

The bacterial cytolethal distending toxin (CDT) was previously shown to block the cell cycle of several cell lines at stage G2 through inactivation of the cyclin-dependent kinase Cdkl and without induction of DNA strand breaks. In the present study, we have analyzed, using various methods of analytical cytometry, the progressive transformation and delayed lethal events in the tumor-derived HeLa cell line temporarily exposed to CDT. The cell proliferation arrest induced by CDT was irreversible but, starting about two days after exposure, the G2 block released partially, concomitantly with a decline in the level of Cdkl phosphorylation. This partial release resulted in endoreduplication, lead…

HistologyTime FactorsCytolethal distending toxinCell divisionAntimetabolitesCell Survival[SDV]Life Sciences [q-bio]Bacterial ToxinsMitosisApoptosisKINASE CYCLIQUE DEPENDANTEBiologyCyclin BPathology and Forensic MedicineCDC2 Protein KinaseEndoreduplicationHumansCyclin B1PhosphorylationMitosisCentrosomeCell DeathCell growthCell BiologyGeneral MedicineCell cycleFlow CytometryVirologyMolecular biologyImmunohistochemistry[SDV] Life Sciences [q-bio]BromodeoxyuridineMicroscopy FluorescenceCell cultureApoptosisCell DivisionHeLa Cells
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Flow cytometry analyses and bioinformatics: interest in new softwares to optimize novel technologies and to favor the emergence of innovative concept…

2007

Histologymedicine.diagnostic_testComputer scienceComputational BiologyCell BiologyBioinformaticsFlow CytometryPathology and Forensic MedicineFlow cytometryCell Physiological PhenomenaSoftware DesignmedicineSoftwareFluorescent DyesCytometry. Part A : the journal of the International Society for Analytical Cytology
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Multiparametric characterization by flow cytometry of flow-sorted subpopulations of a human hepatoma cell line useful for drug research

2004

Background Primary cultured hepatocytes are the closest model to the liver for drug research. However, to overcome its limited availability, the search for hepatic cell lines as an alternative to primary cultures is a matter of current interest. In particular, highly differentiated hepatocellular carcinomas have been proposed as in vitro tools for routine experiments in hepatotoxicity and drug metabolism. Methods Cell populations were selected by fluorescence-activated cell sorting based on low and high relative expressions of P-glycoprotein. These cell lines were characterized after 21 days in culture by multiparametric analysis with flow cytometry providing direct information on key cellu…

Histologymedicine.diagnostic_testIntracellular pHCellCell BiologyBiologyCell sortingMolecular biologyPathology and Forensic MedicineFlow cytometryCell biologymedicine.anatomical_structureCell culturemedicineHepatic stellate cellIntracellularDrug metabolismCytometry Part A
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Diagnosing HIV infection using flow cytometry: From antigenic analyses to a specifically dedicated bead-based assay to measure viral load.

2009

SINCE the discovery of HIV in 1984 (1,2), millions have been infected and have died of AIDS. In 2006, the World Health Organization identified 40 million HIV-infected subjects, noting that antiretroviral therapy was required throughout the world (Fig. 1; http://www.who.int/hiv/data/en/index.html). Today, the situation is very similar and the HIV pandemic remains a major world health problem (3). The treatment of AIDS with highly active antiretroviral therapy (HAART) involves regular monitoring of different blood parameters, requiring the development of convenient and accurate methods that can evaluate HIV infection even in resource-poor countries (4,5). In addition to CD4 cell count, which …

Histologymedicine.diagnostic_testbusiness.industryHIV InfectionsCell BiologyViral Loadmedicine.diseaseFlow CytometryVirologyPolymerase Chain ReactionVirusPathology and Forensic MedicineFlow cytometryBlood serumAcquired immunodeficiency syndrome (AIDS)AntigenImmunologymedicineHumansRNA extractionbusinessCytometryViral loadCytometry. Part A : the journal of the International Society for Analytical Cytology
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