Search results for "Viability"

showing 10 items of 402 documents

As2O3-induced oxidative stress and cycle progression in a human intestinal epithelial cell line (Caco-2)

2007

Foods and drinking water are the main routes for human exposure to inorganic arsenic, the intestinal epithelium being the first barrier against such exogenous toxicants. The present study evaluates the effect of As(III) (0.5-25 microM) upon Caco-2 cells as an intestinal epithelia model. Cell viability, intracellular formation of reactive oxygen species (ROS), mitochondrial membrane potential (Deltapsim) changes, and cell cycle distribution in exposed cultures were evaluated. The intracellular production of ROS was seen to increase in a non-dose dependent manner at all concentrations tested, with impairment of cell mitochondrial enzyme function secondary to a loss of Deltapsim. Concentration…

G2 PhaseCell SurvivalCellTetrazolium SaltsOxidative phosphorylationBiologyToxicologymedicine.disease_causeArsenicalsMembrane PotentialsArsenic TrioxidemedicineHumansViability assaychemistry.chemical_classificationReactive oxygen speciesCell CycleG1 PhaseOxidesGeneral MedicineCell cycleIntestinal epitheliumMitochondriaCell biologyOxidative StressThiazolesmedicine.anatomical_structurechemistryMitochondrial MembranesCaco-2 CellsReactive Oxygen SpeciesOxidative stressIntracellularToxicology in Vitro
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A novel approach for the improvement of stress resistance in wine yeasts

2006

During wine production yeast cells are affected by several stress conditions that could affect their viability and fermentation efficiency. In this work we describe a novel genetic manipulation strategy designed to improve stress resistance in wine yeasts. This strategy involves modifying the expression of the transcription factor MSN2, which plays an important role in yeast stress responses. The promoter in one of the genomic copies of this gene has been replaced by the promoter of the SPI1 gene, encoding for a cell wall protein of unknown function. SPI1 is expressed at late phases of growth and is regulated by Msn2p. This modification allows self-induction of MSN2 expression. MSN2 gene tr…

GeneticsWineSPI1TemperatureRNA FungalWineSaccharomyces cerevisiaeGeneral MedicineBiologyMicrobiologyYeastGenetically modified organismCell biologyIndustrial MicrobiologyKineticsYeast in winemakingStress PhysiologicalGene Expression Regulation FungalFermentationHumansViability assayGeneTranscription factorFood ScienceInternational Journal of Food Microbiology
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FACTORS AFFECTING CHINESE HAMSTER OVARY CELL PROLIFERATION AND VIABILITY

2019

Advantageous cultivation procedures for the Chinese hamster ovary (CHO) cells are necessary for the productive commercial production of biopharmaceuticals. A main challenge that needs to be addressed during the process development is the differences in each cell line requirements concerning the nutrients and feed strategies in order to achieve the desired growth characteristics. Therefore, within the current research, a naïve high cell density serum free suspension adapted CHO cell line was tested with glucose and glutamine rich feeds in fed-batch Erlenmeyer shake flask cultures. Glucose consumption rate was adjusted to develop the optimal feed strategies. Obtained results indicated that hi…

GlutamineNutrientErlenmeyer flasklawCell growthChemistryCell cultureChinese hamster ovary cellViability assayFood scienceMaximum Cell Densitybiotechnology; cell proliferation; Chinese hamster ovary cells; feeding strategylaw.inventionENVIRONMENT. TECHNOLOGIES. RESOURCES. Proceedings of the International Scientific and Practical Conference
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Oxidative stress tolerance, adenylate cyclase, and autophagy are key players in the chronological life span of Saccharomyces cerevisiae during winema…

2012

Most grape juice fermentation takes place when yeast cells are in a nondividing state called the stationary phase. Under such circumstances, we aimed to identify the genetic determinants controlling longevity, known as the chronological life span. We identified commercial strains with both short (EC1118) and long (CSM) life spans in laboratory growth medium and compared them under diverse conditions. Strain CSM shows better tolerance to stresses, including oxidative stress, in the stationary phase. This is reflected during winemaking, when this strain has an increased maximum life span. Compared to EC1118, CSM overexpresses a mitochondrial rhodanese gene-like gene, RDL2, whose deletion lead…

Growth mediumMicrobial ViabilityEcologybiologyGene Expression ProfilingAutophagySaccharomyces cerevisiaeAdenylate kinaseWineSaccharomyces cerevisiaeProtein degradationbiology.organism_classificationApplied Microbiology and BiotechnologyCyclaseYeastchemistry.chemical_compoundOxidative StressBiochemistrychemistryStress PhysiologicalAutophagyMaximum life spanFood ScienceBiotechnologyAdenylyl Cyclases
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Activation of a caspase-3-independent mode of cell death associated with lysosomal destabilization in cultured human retinal pigment epithelial cells…

2008

International audience; Purpose: To characterize the possible cytotoxic effects of oxysterols (7-hydroxycholesterol (7-OH), 25-hydroxycholesterol (25-OH)) in human retinal pigment epithelial cells (ARPE-19) and to detail the relationships between some of these effects. Methods: ARPE-19 cells were treated with 7-OH and 25-OH. Cell viability was measured with the MTT assay. Membrane permeability, mitochondrial potential, and lysosomal integrity were measured by flow cytometry with propidium iodide, DiOC6(3), and acridine orange, respectively. Cell death was characterized by staining with Hoechst 33342, transmission electron microscopy, and analysis of the DNA fragmentation pattern. Caspase ac…

HUMAN BRUCHS MEMBRANECell Membrane PermeabilityMembrane PotentialsAGE-RELATED MACULOPATHYchemistry.chemical_compound0302 clinical medicineFluorescent Antibody Technique IndirectPigment Epithelium of EyeCaspaseCells CulturedElectrophoresis Agar Gel0303 health sciencesbiologyCell DeathCaspase 3CHOLESTEROLAcridine orangeApoptosis Inducing FactorCytochromes cDipeptidesKetonesFlow CytometrySensory SystemsCell biologyMitochondrial MembranesDNA fragmentationCOLORIMETRIC ASSAYMembrane permeabilityCell SurvivalBlotting WesternLOW-DENSITY-LIPOPROTEINCaspase 3DNA FragmentationCysteine Proteinase Inhibitors03 medical and health sciencesCellular and Molecular NeuroscienceBASAL DEPOSITSAPOPTOSIS-INDUCING FACTORHumansRPE CELLSViability assayPropidium iodide[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs030304 developmental biologyMACULAR DEGENERATIONMolecular biologyHydroxycholesterolsEnzyme ActivationOphthalmologychemistryApoptosis030221 ophthalmology & optometrybiology.proteinLysosomes7-KETOCHOLESTEROL-INDUCED APOPTOSIS[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
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Biological properties of carotenoids extracted from Halobacterium halobium isolated from a Tunisian solar saltern

2013

Abstract Background Bioactive molecules have received increasing attention due to their nutraceutical attributes and anticancer, antioxidant, antiproliferative and apoptosis-inducing properties. This study aimed to investigate the biological properties of carotenoids extracted from Archaea. Methods Halophilic Archaea strains were isolated from the brine of a local crystallizer pond (TS7) of a solar saltern at Sfax, Tunisia. The most carotenoid-producing strain (M8) was investigated on heptoma cell line (HepG2), and its viability was assessed by the MTT-test. The cells were incubated with different sub-lethal extract rates, with carotenoid concentrations ranging from 0.2 to 1.5 μM. Antioxida…

HalobacteriumTunisiaAntioxidantCell Survivalmedicine.medical_treatmentHepG2 human cancer cellsArchaea Halobacteria Solar saltern Carotenoids HepG2 human cancer cellsBiologymedicine.disease_causeAntioxidantsMicrobiologyHalobacteriachemistry.chemical_compoundNutraceuticalSettore BIO/10 - BiochimicamedicineHumansSeawaterViability assayFood scienceSettore BIO/06 - Anatomia Comparata E CitologiaCell ShapeCarotenoidchemistry.chemical_classificationSolar salternHep G2 CellsGeneral MedicineArchaeaCarotenoidsHalophileOxidative StressComplementary and alternative medicinechemistryCell cultureArachidonic acidOxidative stressResearch Article
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Patient Segmentation Based on Patient Loyalty

2018

The present study aims to perform a segmentation of patients based on their loyalty behaviour. The analysis focuses on Valencia, a region in Spain that features a capitated financing and free-elective framework; such a framework is particularly suitable for this type of study because patient loyalty directly affects the system’s budget and economic viability. Using secondary data from the regional health council, the study focuses on relationships of influence and latent segmentation in answering seven research questions. The two-pronged statistical analysis is designed to analyse relationships of influence, on the one hand, and latent segmentation, on the other. Significant differences we…

Health Policymedia_common.quotation_subject05 social sciencesApplied psychologyHealth care managementVariable (computer science)Economic viability0502 economics and businessLoyalty050211 marketingStatistical analysisResearch questionsSegmentationPsychology050212 sport leisure & tourismmedia_commonJournal of Health Management
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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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Activation of Human Osteoblasts via Different Bovine Bone Substitute Materials With and Without Injectable Platelet Rich Fibrin in vitro

2021

IntroductionThe aim of the in vitro study was to compare the effect of four bovine bone substitute materials (XBSM) with and without injectable platelet-reach fibrin for viability and metabolic activity of human osteoblasts (HOB) as well as expression of alkaline phosphatase (ALP), bone morphogenetic protein 2 (BMP-2), and osteonectin (OCN).Materials and MethodsCerabone® (CB), Bio-Oss® (BO), Creos Xenogain® (CX) and MinerOss® X (MO) ± i-PRF were incubated with HOB. At day 3, 7, and 10, cell viability and metabolic activity as well as expression of ALP, OCN, and BMP-2, was examined.ResultsFor non-i-PRF groups, the highest values concerning viability were seen for CB at all time points. Pre-t…

Histologyplatelet rich fibrin (PRF)proliferationlcsh:BiotechnologyBiomedical EngineeringBioengineering02 engineering and technologyBone morphogenetic protein 2vitalityFibrinAndrology03 medical and health sciences0302 clinical medicinelcsh:TP248.13-248.65medicineViability assaybovine boneOriginal ResearchbiologyChemistryBioengineering and Biotechnologyin vitroOsteoblastbone substitute030206 dentistry021001 nanoscience & nanotechnologydigestive system diseasesPlatelet-rich fibrinIn vitroPCRmedicine.anatomical_structureosteoblastbiology.proteinAlkaline phosphataseOsteonectin0210 nano-technologyBiotechnologyFrontiers in Bioengineering and Biotechnology
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Apoptosis and cell growth arrest in A375 human melanoma cells by diorganotin(IV) and triorganotin(IV) complexes of [meso-Tetra(4-sulfonatophenyl)porp…

2011

In previous studies we have demonstrated that two derivatives of meso-Tetra(4-sulfonatophenyl)porphine (TPPS), (Bu2Sn)2TPPS and (Bu3Sn)4TPPS, cause apoptotic death of A375 melanoma cells and, at lower concentrations, arrest of cell proliferation. In the present study, we examined if the manganese metal inside the porphyrin cavity could improve the efficacy of this class of compounds. Thus, [meso- Tetra(4-sulfonatophenyl)porphine]Mn(III)Cl (=MnTPPS) derivatives, namely (Me2Sn)2MnTPPS, (Bu2Sn)2MnTPPS, (Me3Sn)4MnTPPS and (Bu3Sn)4MnTPPS, were tested on the A375 human melanoma cell line. A cytotoxicity assay showed that (Bu2Sn)2MnTPPS and (Bu3Sn)4MnTPPS were highly cytotoxic by inducing apoptosi…

HoechstCancer ResearchPorphyrinsSkin NeoplasmsMetalloporphyrinsDrug Evaluation PreclinicalAntineoplastic AgentsApoptosisDNA Fragmentationß-cateninBiology010402 general chemistry01 natural sciencesChloridesc-mycCell Line TumorsnailOrganotin CompoundsHumansCytotoxic T cellViability assayCytotoxicityMelanomacell viabilityCell Proliferation010405 organic chemistryCell growthCell cycleMolecular biology0104 chemical sciences3. Good healthManganese CompoundsOncologyCell cultureApoptosisDNA fragmentationcell viability; ß-catenin; c-myc; snail; HoechstInternational Journal of Oncology
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