Search results for "Cell size"

showing 10 items of 49 documents

Pooled analysis of monocyte distribution width in subjects with SARS‐CoV‐2 infection

2021

2019-20 coronavirus outbreakCoronavirus disease 2019 (COVID-19)Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Clinical BiochemistryLetter to the EditorsMonocytesLeukocyte CountMDWmedicineDistribution (pharmacology)Humansmonocyte distribution widthLetter to the EditorCell SizeBiochemistry medicalbusiness.industrySARS-CoV-2MonocyteBiochemistry (medical)COVID-19Meta-analysis monocyte distribution width MDW SARS-CoV-2HematologyGeneral MedicinePrognosisVirologyMeta-analysisPooled analysismedicine.anatomical_structurebusinessInternational Journal of Laboratory Hematology
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A proton-translocating H+-ATPase is involved in C6 glial pH regulation.

1998

AbstractGlial cells extrude acid equivalents to maintain pHi. Although four mechanisms have been described so far, pHi-control under physiological conditions is still not sufficiently explained. We therefore investigated whether a H+-translocating ATPase is involved in glial pHi homeostasis using an established glial cell line (C6 glioma). In the absence of bicarbonate, the inhibition of H+-ATPases by NEM led to a pHi decrease. The application of a more specific inhibitor (NBD-Cl) showed that the H+-ATPase involved is of the vacuolar type. Inhibition went along with delayed cell swelling. Together with the fact that glial acidification was far more pronounced in Na+-free media, this may ser…

Intracellular FluidBicarbonateATPaseBiophysicsStimulationpHi-regulationBiochemistrychemistry.chemical_compoundEquivalentCell volumemedicineTumor Cells CulturedAnimalsCell SizebiologyChemistryBiological TransportC6 gliomaVacuolar type H+-ATPaseCell BiologyGliomaHydrogen-Ion ConcentrationAmilorideCell biologyCulture MediaRatsProton-Translocating ATPasesmedicine.anatomical_structureCell culturebiology.proteinProtonsAstrocyteAcidsHomeostasismedicine.drugAstrocyteBiochimica et biophysica acta
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Endothelial Cell Swelling and Brain Perfusion

1997

Background: Whereas the contribution of glial swelling to no-reflow conditions in the ischemic penumbra or during reperfusion after global ischemia is widely discussed, little is known about cell volume control of endothelial cells under reperfusion conditions. Methods: The effect of extracellular acidosis-a key mediator of secondary brain damage-on cell volume was studied in the GM7373 endothelial cell line. Experiments were performed at pH = 6.0 in the presence or absence of bicarbonate, and during exposure to inhibitors of specific transport systems such as ethyl isopropyl amiloride or 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid. Results: Endothelial swelling to 111.1 ± 3.4% was f…

medicine.medical_specialtyCell Membrane PermeabilityBicarbonateIschemiaPharmacologyBrain IschemiaCell Linechemistry.chemical_compoundmedicineExtracellularAnimalsCell Sizebusiness.industryMicrocirculationPenumbraHydrogen-Ion Concentrationmedicine.diseaseAmilorideSurgeryEndothelial stem cellchemistryCerebrovascular CirculationReperfusion InjuryCattleEndothelium VascularSwellingmedicine.symptomAcidosisbusinessIsopropylmedicine.drugThe Journal of Trauma: Injury, Infection, and Critical Care
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pRb suppresses camptothecin-induced apoptosis in human osteosarcoma Saos-2 cells by inhibiting c-Jun N-terminal kinase

2001

AbstractThis paper studies the cytotoxic effect induced by the topoisomerase I inhibitor camptothecin in human osteosarcoma Saos-2 cells, which lack p53 and contain a non-functional form of the product of the retinoblastoma gene, pRb. Cytotoxicity induced by camptothecin was dose- and time-dependent; the treatment with 100 nM camptothecin reduced cell viability by 50% at 32 h and by 75% at 72 h of exposure. The cytotoxic effect was caused by apoptosis, as ascertained by morphological evidence, acridine orange-ethidium bromide staining and flow cytometric analysis. Apoptosis was accompanied by both the activation of caspase-3 and the fragmentation of poly(ADP-ribose) polymerase. Treatment wi…

Time FactorsCell SurvivalProto-Oncogene Proteins c-junBlotting WesternBiophysicsApoptosisBiologyTransfectionRetinoblastoma ProteinBiochemistryStructural BiologyTumor Cells CulturedpRb JNK topoisomerase I inhibitors osteosarcomaGeneticsmedicineHumansCytotoxic T cellViability assayPhosphorylationFragmentation (cell biology)neoplasmsMolecular BiologySaos-2 cellsc-Jun N-terminal kinaseCell SizeDose-Response Relationship DrugCaspase 3Cell growthCell Cyclec-junJNK Mitogen-Activated Protein KinasesHydrogen PeroxideCell BiologyFlow CytometryGlutathioneMolecular biologyEnzyme ActivationOxidative StresspRbDNA Topoisomerases Type IApoptosisCaspasesCamptothecinMitogen-Activated Protein KinasesPoly(ADP-ribose) PolymerasesTopoisomerase I InhibitorsCamptothecinmedicine.drugFEBS Letters
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Endothelial study of iris-claw phakic lens: four year follow-up.

1998

Abstract Purpose: To study quantitative and morphometric endothelial changes in phakic eyes implanted with the Worst iris-claw lens to correct high myopia. Setting: Department of Ophthalmology, University Hospital “La Fe”, Valencia, Spain. Material and Methods: This retrospective study involved 111 phakic eyes (73 patients) implanted with the Worst iris-claw lens. Noncontact specular microscopy and computer-assisted analysis was performed preoperatively and 6 months and 1, 2, 3, and 4 years postoperatively. Results: The mean cell loss was 3.85% at 6 months, 6.59% at 1 year, 9.22% at 2 years, 11.68% at 3 years, and 13.42% at 4 years. At 2 years, the hexagonality and coefficient variation in …

AdultMaleReoperationmedicine.medical_specialtyRefractive errorVisual acuitygenetic structuresAnterior Chambermedicine.medical_treatmentEye diseaseCorneal TouchVisual AcuityIrisIntraocular lensCell CountPhakic intraocular lensCorneal DiseasesVision disorderPostoperative ComplicationsLens Implantation IntraocularOphthalmologyCorneaMyopiaMedicineHumansCell SizeRetrospective Studiesbusiness.industryEndothelium CornealMiddle Agedmedicine.diseaseeye diseasesSensory SystemsSurgeryOphthalmologymedicine.anatomical_structureSurgeryFemalesense organsmedicine.symptombusinessFollow-Up StudiesJournal of cataract and refractive surgery
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Similar morphokinetic patterns in embryos derived from obese and normoweight infertile women: a time-lapse study.

2013

Study question Does female obesity affect the dynamic parameters of embryo quality assessed by time-lapse analysis? Summary answer Female obesity does not affect the dynamic embryo quality as determined by image acquisition and time-lapse analysis. What is known already Female obesity impairs natural and assisted reproduction but there is no agreement on the specific contribution of gametes, embryos or endometrial receptivity. In this preliminary study the dynamic parameters of embryo quality are assessed for the first time by time-lapse analysis. Study design, size, duration Two-year cohort retrospective study comparing embryos from three groups of patients according to the presence of inf…

InfertilityAdultmedicine.medical_specialtyTime-Lapse ImagingBody Mass IndexAndrologyCohort StudiesEmbryo Culture TechniquesmedicineImage Processing Computer-AssistedHumansObesityCell SizeRetrospective StudiesGynecologyOocyte Donationbusiness.industryRehabilitationObstetrics and GynecologyRetrospective cohort studyEmbryoOocytemedicine.diseaseKineticsmedicine.anatomical_structureBlastocystReproductive Medicineembryonic structuresCohortEctogenesisFemalebusinessBody mass indexInfertility FemaleEmbryo qualityCell DivisionCohort studyHuman reproduction (Oxford, England)
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Anaemia in advanced chronic fasciolosis

2008

Abstract The association between fasciolosis-induced anaemia and related factors has been quantified in a rodent model. Haematological parameters were analysed in Wistar rats at 20 and 60 weeks post-infection (p.i.). Pigment stones and bile specimens were collected. Serum IgG1, IgG2a and IgE were determined in rat serum samples. Cytokine levels have been correlated with haematological parameters. The screening for gastrointestinal bleeding was carried out. Bacteriological bile cultures revealed viable bacteria in 53.8% of specimens at 60 weeks p.i. The results show that the type of anaemia in fasciolosis might be considered a biomarker of the chronicity period of the disease, changing from …

Fascioliasismedicine.medical_specialtyAnemiaVeterinary (miscellaneous)Statistics as TopicAntibodies HelminthHelminthiasisPhysiologyBiologyFecesInternal medicinemedicineAnimalsBileFasciolosisRats WistarEggs per gramFecesCell SizeAnemia HypochromicMicrobial ViabilityHematologyBacteriaAnemiamedicine.diseaseHaemolysisRatsInfectious DiseasesInsect ScienceMultivariate AnalysisImmunologyErythropoiesisParasitologyBiomarkersSpleenActa Tropica
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An Artificial Neural Network Assisted Dynamic Light Scattering Procedure for Assessing Living Cells Size in Suspension

2020

Dynamic light scattering (DLS) is an essential technique used for assessing the size of the particles in suspension, covering the range from nanometers to microns. Although it has been very well established for quite some time, improvement can still be brought in simplifying the experimental setup and in employing an easier to use data processing procedure for the acquired time-series. A DLS time series processing procedure based on an artificial neural network is presented with details regarding the design, training procedure and error analysis, working over an extended particle size range. The procedure proved to be much faster regarding time-series processing and easier to use than fitti…

LightComputer sciencesimulated time-series02 engineering and technologySaccharomyces cerevisiaelcsh:Chemical technology01 natural sciencesBiochemistryArticleAnalytical Chemistry010309 optics<i>Saccharomyces cerevisiae</i>Dynamic light scatteringSuspensions0103 physical sciencesRange (statistics)Scattering Radiationlcsh:TP1-1185Electrical and Electronic EngineeringParticle SizeSuspension (vehicle)InstrumentationfermentationCell SizeAqueous solutionArtificial neural networkdynamic light scatteringFunction (mathematics)021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsParticle sizeNeural Networks Computer0210 nano-technologyBiological systemartificial neural networkSensors
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Isolation and molecular characterization of brain microvascular endothelial cells from human brain tumors.

2002

Brain tumor formation and growth is accompanied by the proliferation and infiltration of blood capillaries. The phenotypes of endothelial cells that make up capillaries are known to differ not only in the tissues in which endothelial cells are located but also as a result of the microenvironment to which they are exposed. For this reason, primary cultures of brain endothelial cells were isolated from human brain tumors removed by surgery and compared with cells from normal tissue. The primary confluent monolayers that grew out of isolated capillary fragments consisted of closely associated, elongated, fusiform-shaped cells. But brain tumor-derived endothelial cells in culture exhibited sign…

Vascular Cell Adhesion Molecule-1Cell SeparationBiologyBlood–brain barrierAntigenvon Willebrand FactormedicineTumor Cells CulturedHumansCell adhesionCell SizeFluorescent DyesTight junctionBrain NeoplasmsBrainMembrane ProteinsCell BiologyGeneral MedicineHuman brainCarbocyaninesmedicine.diseaseIntercellular Adhesion Molecule-1PhosphoproteinsCell biologyMicroscopy Electronmedicine.anatomical_structureCell cultureBlood-Brain BarrierZonula Occludens-1 ProteinEndothelium VascularStem cellPlant LectinsE-SelectinInfiltration (medical)Developmental BiologyIn vitro cellulardevelopmental biology. Animal
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An in vitro model to study cellular photosensitizer uptake and photodynamic dose-response relationships of tumor cells

1993

Cellular fluorescence intensity (CFI) after incubation with varying concentrations of the photosensitizer Photofrin and the photodynamically induced dose-response relationships of hamster melanoma cells (A-MEL-3) were studied in a recently developed in vitro model. After administration of Photofrin to the extracellular serum-free medium, CFI was evaluated by flow cytometry together with constantly fluorescing latex particles used as a reference. After 5 min, 50% of maximal CFI was found, and after 60 min CFI was maximal. No further increase was obtained during the exposure to Photofrin over the incubation period of 4 h. During this plateau phase, CFI was significantly related to the concent…

Pathologymedicine.medical_specialtyCell SurvivalMelanoma ExperimentalHamsterIn Vitro TechniquesBiologyFluorescenceFlow cytometrychemistry.chemical_compoundIn vivoCricetinaeTumor Cells CulturedExtracellularmedicineAnimalsPhotosensitizerViability assayCell SizeDose-Response Relationship DrugMesocricetusmedicine.diagnostic_testGeneral MedicineFlow CytometryPhotochemotherapychemistryBiophysicsDihematoporphyrin EtherTrypan bluePhototoxicityResearch in Experimental Medicine
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