Search results for "Cytometry"

showing 10 items of 852 documents

Automated DNA-image cytometry: a prognostic tool in infiltrating bladder carcinoma?

1987

In a retrospective study, paraffin-embedded cystectomy specimens obtained from 46 patients with bladder cancer (stage pT1 — pT4a, pN0, pN2) were analysed for tumor DNA ploidy and proliferation using automated image cytometry (LEYTAS). In 41 cases, DNA ploidy could be measured. Estimation of proliferation was possible in 26 tumors. The number of cells with a DNA content higher than 5C could be calculated in 38 of the tumors. All these three parameters are shown to correlate with patient outcome.

Pathologymedicine.medical_specialtyBladder cancerUrinary bladderbusiness.industryUrologymedicine.medical_treatmentmedicine.diseaseCystectomychemistry.chemical_compoundmedicine.anatomical_structurechemistryCarcinomamedicineStage (cooking)businessCytometryDNADNA Image CytometryWorld Journal of Urology
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Infarct Size Measurement by Triphenyltetrazolium Chloride StainingVersus In VivoInjection of Propidium Iodide

1997

Infarct size delineation by triphenyltetrazolium chloride (TTC) staining is dependent on sufficient reperfusion. We therefore evaluated the possibility of using propidium iodide (PI), a reagent conventionally used in flow cytometry to fluorescently stain dead cells, for infarct size analysis after short periods of reperfusion. Forty-five rabbits were subjected to either 15 min, 2 h or 4.5 h of coronary artery occlusion without reperfusion, or to 15 min, 30 min and 2 h of coronary artery occlusion followed by 30 min, 1 h and 3 h of reperfusion. Fifteen min before terminating the experiment, PI was injected into the left atrium. Patent blue violet was used to delineate the area at risk. Follo…

Pathologymedicine.medical_specialtyCell Membrane PermeabilityMyocardial InfarctionTetrazolium SaltsMyocardial ReperfusionStainFlow cytometrychemistry.chemical_compoundIn vivoOcclusionmedicineAnimalscardiovascular diseasesPropidium iodideColoring AgentsMolecular BiologyStaining and Labelingmedicine.diagnostic_testChemistrybusiness.industryMyocardiumHistologymedicine.diseaseCoronary VesselsStainingInjections Intra-ArterialRabbitsCardiology and Cardiovascular MedicineNuclear medicinebusinessReperfusion injuryPropidiumJournal of Molecular and Cellular Cardiology
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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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Clinicopathologic and DNA Flow Cytometric Analysis of Eighty-three Renal Cell Carcinomas

1995

The clinical and anatomopathologic features as well as DNA content of 83 renal cell carcinomas were analyzed. The possible interrelationship and prognostic value of these factors were also considered. The DNA study has been performed by flow cytometry using paraffin-embedded tissues. In each case an internal control with nonneoplastic renal tissue obtained in the same nefrectomy was also done in order to calculate the DNA index. Differences in patient age, nuclear grade, and mitotic activity were related with outcome; however, this relationship was not confirmed by the Cox test. Stage (P = .005), cell type (P = .002), and metastatic disease (P = .001) had independent prognostic values. Ren…

Pathologymedicine.medical_specialtyCell typemedicine.diagnostic_testbusiness.industryCellmedicine.diseasePathology and Forensic MedicineFlow cytometrychemistry.chemical_compoundmedicine.anatomical_structurechemistryRenal cell carcinomamedicineSurgeryAnatomyStage (cooking)businessNuclear gradeMitosisDNAInternational Journal of Surgical Pathology
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Adipose tissue sensitivity to radiation exposure

2008

1525-2191 (Electronic) Journal Article Research Support, Non-U.S. Gov't; Treatment of cancer using radiation can be significantly compromised by the development of severe acute and late damage to normal tissue. Treatments that either reduce the risk and severity of damage or that facilitate the healing of radiation injuries are being developed, including autologous adipose tissue grafts to repair tissue defects or involutional disorders that result from tumor resection. Adipose tissue is specialized in energy storage and contains different cell types, including preadipocytes, which could be used for autologous transplantation. It has long been considered a poorly proliferative connective ti…

Pathologymedicine.medical_specialtyCellular differentiationPopulationExperimental/metabolism/*pathologyAdipose tissueConnective tissueCell Proliferation/*radiation effectsBiologyPolymerase Chain ReactionPathology and Forensic MedicineMiceOxidative Stress/radiation effectsmedicineAdipocytesIn Situ Nick-End LabelingAutologous transplantationAnimalsStem Cells/metabolism/pathology/radiation effectsProgenitor celleducationRadiation InjuriesCell Proliferationeducation.field_of_studyStem CellsAdipocytes/cytology/metabolism/*radiation effectsCell DifferentiationTotal body irradiationFlow CytometryImmunohistochemistryAdipose Tissue/cytology/*radiation effectsOxidative StressRadiation Injuries ExperimentalCell Differentiation/*radiation effectsmedicine.anatomical_structurePhenotypeAdipose TissueStem cellRegular Articles
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Contrasting responses of Kupffer cells and inflammatory mononuclear phagocytes to biliary obstruction in a mouse model of cholestatic liver injury.

2012

Background Biliary obstruction and cholestasis are serious complications of many liver diseases. Although resident hepatic macrophages (Kupffer cells) are frequently implicated in disease progression, most studies fail to differentiate the contribution of Kupffer cells and inflammatory mononuclear phagocytes (iMNPs) that infiltrate the liver subsequent to obstruction. Aim This study was undertaken to examine the roles and potential interactions of these two disparate mononuclear phagocyte populations in hepatic injury attending cholestasis. Methods Female, C57Bl/6 mice were injected with magnetic beads on day 3 prior to sham operation or bile duct ligation (BDL) to facilitate subsequent Kup…

Pathologymedicine.medical_specialtyChemokineLiver cytologyKupffer Cellsmedicine.medical_treatmentInflammationCholestasis IntrahepaticBiologyReal-Time Polymerase Chain Reactiondigestive systemMiceCholestasismedicineAnimalsMononuclear Phagocyte SystemLiver injuryHepatologyKupffer cellMononuclear phagocyte systemmedicine.diseaseFlow CytometrySpecific Pathogen-Free OrganismsMice Inbred C57BLmedicine.anatomical_structureCytokineImmunologybiology.proteinFemalemedicine.symptomLiver international : official journal of the International Association for the Study of the Liver
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Wharton's Jelly Stem Cells: A Novel Cell Source for Oral Mucosa and Skin Epithelia Regeneration

2013

Abstract Perinatal stem cells such as human umbilical cord Wharton's jelly stem cells (HWJSCs) are excellent candidates for tissue engineering because of their proliferation and differentiation capabilities. However, their differentiation potential into epithelial cells at in vitro and in vivo levels has not yet been reported. In this work we have studied the capability of HWJSCs to differentiate in vitro and in vivo to oral mucosa and skin epithelial cells using a bioactive three-dimensional model that mimics the native epithelial-mesenchymal interaction. To achieve this, primary cell cultures of HWJSCs, oral mucosa, and skin fibroblasts were obtained in order to generate a three-dimension…

Pathologymedicine.medical_specialtyFluorescent Antibody TechniqueMice NudeFilaggrin ProteinsBiologyModels BiologicalEpitheliumMiceIntermediate Filament ProteinsTissue engineeringTissue Engineering and Regenerative MedicineWharton's jellymedicineAnimalsHumansRegenerationWharton JellyProtein PrecursorsOral mucosaInvolucrinSkinRegeneration (biology)Mouth MucosaCell DifferentiationEpithelial CellsMesenchymal Stem CellsCell BiologyGeneral MedicineFlow CytometryCell biologymedicine.anatomical_structureCell cultureKeratinsLeukocyte Common AntigensThy-1 Antigensgamma CateninStem cellDevelopmental BiologyAdult stem cellStem Cells Translational Medicine
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Clinical Cytometry in Europe, 2010

2010

Pathologymedicine.medical_specialtyHistologybusiness.industryMedicineCell BiologybusinessCytometryPathology and Forensic MedicineCytometry Part B: Clinical Cytometry
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Utility of CD54, CD229, and CD319 for the identification of plasma cells in patients with clonal plasma cell diseases

2015

Background Multiparameter flow cytometry (MFC) identification and characterization of plasma cells (PCs) is a useful tool to support diagnosis, prognostication, and monitoring of PC diseases (PCD). Currently, the number of MFC markers suited for the identification of PC remains limited. Moreover, antibody therapies against PC-associated markers further compromise the utility of the most widely used reagents (e.g., CD38). Despite markers other than CD38 and CD138 are recognized as potentially useful PC-identification markers, no study has comparatively evaluated their performance in combination with CD38 and CD138. Here we compared the utility of CD229, CD54, and CD319 for the identification…

Pathologymedicine.medical_specialtyHistologymedicine.diagnostic_testCell BiologyBiologyPlasma cellmedicine.diseaseMinimal residual diseasePathology and Forensic MedicineFlow cytometry03 medical and health sciences0302 clinical medicineImmunophenotypingmedicine.anatomical_structureimmune system diseasesEuroFlowhemic and lymphatic diseases030220 oncology & carcinogenesismedicineBone marrowCytometryMultiple myeloma030215 immunologyCytometry Part B: Clinical Cytometry
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CD133 expression is associated with small round blue cell tumour morphology in human central nervous system neoplasms

2011

Schittenhelm J, Simon P, Harter P N, Zachskorn C, Schlaszus H, Rottger F, Winkels M, Weller M, Meyermann R & Mittelbronn M (2011) Histopathology58, 739–749 CD133 expression is associated with small round blue cell tumour morphology in human central nervous system neoplasms Aims:  CD133 is considered to be a marker for brain tumour-initiating cells. However, most data on CD133 are derived from animal or in-vitro studies. The aim of this study was to characterize CD133 expression, and the distribution and morphological features of CD133+ cells, in primary and secondary human central nervous system (CNS) neoplasms. Methods and results:  Tumours were analysed by real-time reverse transcription …

Pathologymedicine.medical_specialtyHistologymedicine.diagnostic_testCellular differentiationCellGeneral MedicineCD15NestinBiologyStem cell markerPathology and Forensic MedicineFlow cytometrycarbohydrates (lipids)Reverse transcription polymerase chain reactionfluids and secretionsmedicine.anatomical_structureembryonic structurescardiovascular systemmedicineCancer researchStem cellneoplasmsHistopathology
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