Search results for "Cytochemistry"

showing 10 items of 178 documents

Region specific expression of furin mRNA in the rat brain.

1993

The distribution of furin mRNA was examined in the rat central nervous system. Northern blot analysis reveals the presence of a 4.4 kb band in all brain tissues examined. In situ hybridization analysis of frozen rat brain sections using a radioactively labeled antisense cRNA probe to rat furin demonstrated moderate to low levels of expression in both neuronal and non-neuronal tissue in all areas examined. Interestingly, higher levels of furin were expressed in selective regions which include the ventricles (the choroid plexus and ependymal cells), the islands of Calleja, the hippocampus and the pineal gland. the ubiquitous localization of furin in the brain is consistent with its postulated…

Malemedicine.medical_specialtyanimal structuresvirusesProprotein convertase 2In situ hybridizationRats Sprague-DawleyInternal medicineGene expressionmedicineAnimalsTissue DistributionNorthern blotRNA MessengerSubtilisinsFurinIn Situ HybridizationFurinbiologyHistocytochemistryGeneral NeuroscienceSerine EndopeptidasesBrainCell biologyRatsEndocrinologymedicine.anatomical_structureProprotein Convertase 2embryonic structuresIslands of Callejabiology.proteinChoroid plexusProprotein ConvertasesEpendymaNeuroscience letters
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A monoclonal antibody against an adult-specific cuticular protein of Tenebrio molitor (Insecta, Coleoptera)

1989

International audience; To study the sequential expression of the epidermal program in the mealworm Tenebrio molitor, monoclonal antibodies were prepared against the water-soluble proteins from preecdysial adult cuticle. Among the 16 clones obtained, one of them (named K2F6) recognized a 20-kDa antigen, found only in adult extracts but not in the larval or pupal ones, as revealed by immunoblot analysis. Our results strongly suggest an epidermal origin for this protein. The monoclonal antibody K2F6 fails to react with water-soluble proteins from fat body and hemolymph taken during the deposition of the 20-kDa antigen. Electron microscopic immunogold localization of this antigen showed that i…

Mealwormmedicine.drug_classCuticle[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionImmunocytochemistryBlotting WesternMonoclonal antibodyAntigenImmunoblot AnalysisHemolymph[SDV.BDD] Life Sciences [q-bio]/Development BiologymedicineAnimals[ SDV.BDD ] Life Sciences [q-bio]/Development BiologyTenebrioMolecular Biology[SDV.BDD]Life Sciences [q-bio]/Development BiologybiologyAntibodies MonoclonalProteinsCell BiologyImmunogold labellingbiology.organism_classificationMolecular biologyImmunohistochemistryJuvenile HormonesMolecular Weight[SDV.AEN] Life Sciences [q-bio]/Food and NutritionMicroscopy ElectronImmunologyEpidermis[SDV.AEN]Life Sciences [q-bio]/Food and NutritionBiomarkersDevelopmental Biology
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Increased innate and adaptive immune responses in induced sputum of young smokers

2015

Background and objectives: It is known that chronic obstructive pulmonary disease (COPD) development process is imperceptible and can be asymptomatic for 20 or more years. It is of great importance to diagnose early inflammatory changes that can lead to COPD in young asymptomatic cigarette smokers. The aim of our study was to analyze the cell spectrum of induced sputum (IS) of young cigarette smokers, with emphasis on T-regulatory cells. Materials and methods: A total of 20 healthy nonallergic smokers, 20 nonsmokers and 20 COPD patients were enrolled in the study. After lung function measurements were taken, we performed sputum induction and analyzed sputum cells. We evaluated the cell coun…

Medicine(all)Medicine (General)COPDbusiness.industryChronic obstructive pulmonary diseaseLymphocyteSmokingImmunocytochemistryChronic obstructive pulmonary disease; T regulatory lymphocytes; Sputum induction; Smokingmedicine.diseaseAsymptomaticrespiratory tract diseasesStainingSputum inductionR5-920medicine.anatomical_structureImmune systemAutomotive EngineeringImmunologymedicineSputummedicine.symptombusinessCD8T regulatory lymphocytesMedicina
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Identification of the NO Synthase isoforms Expressed in Human Neutrophil Granulocytes, Megakaryocytes and Platelets

1997

SummaryUsing Western blot and fluorescent immunocytochemistry, NOS III (or ecNOS) and NOS II (or iNOS), but no NOS I (or ncNOS), were identified in preparations of human platelets. Reverse-transcription polymerase chain reactions (RT-PCR) demonstrated NOS III mRNA, but no NOS II mRNA (which is short-lived) and no NOS I mRNA in platelets. Immunofluorescent staining of human bone marrow smears showed the presence of NOS III, but not NOS I in megakaryocytes. A subpopulation of megakaryocytes also expressed NOS II. In preparations of human neutrophils, immunocytochemistry demonstrated NOS I in all cells, whereas no NOS III was detected. The few NOS II positive cells were characterized as contam…

Messenger RNAmedicine.diagnostic_testImmunocytochemistryHematologyGranulocyteBiologyMolecular biologyNitric oxide synthasemedicine.anatomical_structureWestern blotMegakaryocyteGene expressionmedicinebiology.proteinPlateletThrombosis and Haemostasis
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Ultracytochemical localization of Ca2(+)-ATPase activity in the middle ear mucosa of the guinea pig.

1989

Ca2(+)-ATPase activity was studied ultra-cytochemically in the middle ear mucosa of the guinea pig. On electron microscopic examination, the most intense reaction was found on the microvilli. Reaction products were also observed on the cilia and around and between the secretory granules on the apical side of the cells in their secretory phase. The basolateral membranes contained few reaction products, while very little or no activity was found on the basal membrane.

Mucous MembranebiologyMicrovillibusiness.industryATPaseCiliumGuinea PigsEar MiddleGeneral MedicineCalcium-Transporting ATPasesMolecular biologyGuinea pigCalcium ATPaseMembranemedicine.anatomical_structureOtorhinolaryngologyBiochemistryMiddle earbiology.proteinCytochemistryMedicineAnimalsbusinessIon transporterArchives of oto-rhino-laryngology
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A mild juvenile variant of type IV glycogenosis.

1992

The mild juvenile form of type IV glycogenosis, confirmed by a profound deficiency of the brancher enzyme in tissue specimens is reported from three Turkish male siblings who, foremost, suffered from chronic progressive myopathy. Muscle fibers contained polyglucosan inclusions of typical fine structure, i.e. a mixture of granular and filamentous glycogen. They reacted strongly for myophosphorylase, but were resistant to diastase. These inclusions were ubiquitinated and reacted with antibody KM-279 which previously has been shown to bind to Lafora bodies, corpora amylacea and polyglucosan material in hepatic and cardiac cells of type IV glycogenosis as well as polyglucosan body myopathy with…

Muscle tissueMalemedicine.medical_specialtyBiologychemistry.chemical_compoundGlycogen Storage Disease Type IVDevelopmental NeuroscienceInternal medicineSweat glandmedicineHumansGlycogen storage disease type IVMyopathyChildGlycogenStaining and LabelingHistocytochemistryMusclesInfantGeneral Medicinemedicine.diseaseEnzyme assaySweat Glandsmedicine.anatomical_structureEndocrinologychemistryMyophosphorylasePediatrics Perinatology and Child Healthbiology.proteinNeurology (clinical)medicine.symptomCorpora amylaceaBraindevelopment
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Changes of energy metabolism, myosin light chain composition, lactate dehydrogenase isozyme pattern and fibre type distribution of denervated fast-tw…

1985

The influence of low frequency (8-10 Hz) electrical stimulation on denervated fast-twitch muscle from rabbit was investigated. Prolonged direct stimulation of denervated muscle resulted in higher oxidative enzyme activities. Furthermore, single fibre analyses for succinate dehydrogenase showed a more uniform distribution of activity in stimulated-denervated muscle when compared to normal muscle. As was also the case following stimulation of innervated muscle, glycolytic enzymes were decreased in activity and the LDH-isozyme pattern was also shifted towards heart type. No change of the myosin light chain pattern could be observed after 56 days of stimulation.

Myosin light-chain kinaseChemical PhenomenaPhysiologyClinical BiochemistryStimulationMyosinschemistry.chemical_compoundPhysiology (medical)Lactate dehydrogenaseMyosinAnimalsDenervationMuscle DenervationLagomorphaL-Lactate DehydrogenasebiologyHistocytochemistryChemistryMusclesSuccinate dehydrogenasebiology.organism_classificationElectric StimulationMuscle DenervationIsoenzymesChemistrybiology.proteinBiophysicsRabbitsEnergy MetabolismPfl�gers Archiv European Journal of Physiology
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Monoclonal antibodies SMI 311 and SMI 312 as tools to investigate the maturation of nerve cells and axonal patterns in human fetal brain

1998

Neurofilaments, which are exclusively found in nerve cells, are one of the earliest recognizable features of the maturing nervous system. The differential distribution of neurofilament proteins in varying degrees of phosphorylation within a neuron provides the possibility of selectively demonstrating either somata and dendrites or axons. Non-phosphorylated neurofilaments typical of somata and dendrites can be visualized with the aid of monoclonal antibody SMI 311, whereas antibody SMI 312 is directed against highly phosphorylated axonal epitopes of neurofilaments. The maturation of neuronal types, the development of area-specific axonal networks, and the gradients of maturation can thus be …

Nervous systemHistologyNeurofilamentmedicine.drug_classeducationImmunocytochemistryGolgi ApparatusGestational AgeBiologyMonoclonal antibodyPathology and Forensic MedicineEpitopeschemistry.chemical_compoundNeurofilament ProteinsmedicineHumansParaformaldehydeNeuronsPyramidal CellsfungiInfant NewbornAntibodies MonoclonalBrainAbortion InducedDendritesCell BiologyImmunohistochemistryAxonsmedicine.anatomical_structurenervous systemchemistryImmunohistochemistryNeuronNeuroscienceImmunostainingCell and Tissue Research
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Co-expression of heat sensitive vanilloid receptor subtypes in rat dorsal root ganglion neurons

2003

Expression of the heat sensitive cation channels TRPV1 and TRPV2 was investigated by immunofluorescence in rat dorsal root ganglion (DRG) neurons. TRPV1-positive neurons were more frequent and had smaller diameters than TRPV2-positive neurons (35.7% vs 7.3%; 22.3 microm vs 27.6 microm), but size distributions overlapped and significant co-expression was seen in 20.7% of TRPV2-positive neurons (1.7% of all). Expression patterns did not differ between tissue sections typically used in immunocytochemistry and dissociated DRG neurons typically used in electrophysiology. Rectangular temperature pulses revealed two patterns of heat-evoked inward currents in small DRG neurons: low-threshold rapidl…

NeuronsHot TemperatureReceptors DrugGeneral NeuroscienceTRPV2ImmunocytochemistryCentral nervous systemTRPV1TRPV Cation ChannelsBiologySpinal cordRatsRats Sprague-DawleyElectrophysiologymedicine.anatomical_structureGene Expression Regulationnervous systemDorsal root ganglionGanglia SpinalmedicineBiophysicsAnimalsNeuronNeuroscienceNeuroReport
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A combined ex/in vivo assay to detect effects of exogenously added factors in neural stem cells.

2007

We describe a protocol developed/modified by our group for the ex vivo and in vivo assessment of the response to a soluble factor of murine neural stem cells from the adult sub-ventricular zone (SVZ). The procedure includes several experimental options that can be used either independently or in combination. Potential factor effects on self-renewal, survival and proliferation are assayed by means of neurosphere cultures, with the factor administered directly in vitro to the culture plates (Step 1) or infused in vivo immediately before tissue dissociation (Step 3). We also use bromodeoxiuridine (BrdU) retention to label slowly dividing cells in vivo and subsequently perform two different typ…

NeuronsStaining and LabelingStem CellsImmunocytochemistryTransfectionBiologyImmunohistochemistryGeneral Biochemistry Genetics and Molecular BiologyIn vitroNeural stem cellCell biologyCerebral VentriclesMiceBromodeoxyuridineIn vivoNeurosphereAnimalsIntercellular Signaling Peptides and ProteinsStem cellEx vivoCells CulturedNature protocols
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