Search results for "Cytochemistry"

showing 10 items of 178 documents

Synaptophysin expressed in the bronchopulmonary tract: neuroendocrine cells, neuroepithelial bodies, and neuroendocrine neoplasms.

1987

Synaptophysin is an integral membrane glycoprotein with an Mr of 38,000 that occurs in the small, clear vesicles present in neuronal cells and tumors as well as in pancreatic islet cells and various neuroendocrine (NE) carcinomas. We found that synaptophysin is also expressed in normal NE cells of the lungs of newborn rabbits and mice as well as of human fetuses. In bronchial ganglion cells and in nerves, synaptophysin is coexpressed with neurofilament proteins (NFPs), whereas in solitary NE cells and in at least some of the neuroepithelial bodies (NEBs) of the bronchial mucosal lining, synaptophysin coexists with cytokeratins. We also studied a series of NE neoplasms of the lung covering t…

Cancer Researchmedicine.medical_specialtyPathologyLung NeoplasmsCellular differentiationImmunocytochemistrySynaptophysinNeuropeptideFluorescent Antibody TechniqueMiceInternal medicinemedicineAnimalsHumansMolecular BiologyLungImmunoassayLungbiologyDesmoplakinHistocytochemistryMembrane ProteinsCell DifferentiationEpithelial CellsCell BiologyNeurosecretory SystemsGanglionMembrane glycoproteinsEndocrinologymedicine.anatomical_structurenervous systemAnimals NewbornSynaptophysinbiology.proteinKeratinsRabbitsDevelopmental BiologyDifferentiation; research in biological diversity
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Endothelial angiopoietin-2 overexpression in explanted livers identifies subjects at higher risk of recurrence of hepatocellular carcinoma after live…

2022

BackgroundThough the precise criteria for accessing LT are consistently being applied, HCC recurrence (HCC-R_LT) still affects more than 15% of the patients. We analyzed the clinical, histopathological, and biological features of patients with HCC to identify the predictive factors associated with cancer recurrence and survival after LT.MethodsWe retrospectively analyzed 441 patients with HCC who underwent LT in our center. Overall, 70 (15.8%) of them developed HCC-R_LT. We matched them by age at transplant and etiology with 70 non-recurrent patients. A comparable cohort from the Liver Transplant Centre of Bologna served as validation. The clinical and biochemical characteristics and pre-LT…

Cancer ResearchneoangiogenesisimmunocytochemistryrecurrenceOncologyliver transplantationneoangiogenesiangiopoietin-2hepatocellular carcinomaangiopoietin-2; hepatocellular carcinoma; immunocytochemistry; liver transplantation; neoangiogenesis; recurrence; survivalsurvival
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Congenital myopathies - a comprehensive update of recent advancements

2009

The congenital myopathies are relatively newly discovered compared with other categories of muscle diseases. Current research continues to clarify and classify the congenital myopathies. These pose a diagnostic problem and cannot be diagnosed by routine hematoxylin and eosin stain. A lot of special techniques are required to diagnose them correctly and it's various subtypes. The disease specific structural changes seen in the muscle are detected by enzyme histochemistry, immunohistochemistry and electron microscopy. Through this review we provide an up-to-date analysis of congenital myopathies including clinical and pathologic aspects.

Cardiomyopathy DilatedDisease specificPathologymedicine.medical_specialtyH&E stainMuscular DiseasesmedicineHumansGenetic Predisposition to DiseaseMyopathyPathology ClinicalMuscle biopsymedicine.diagnostic_testHistocytochemistrybusiness.industryEnzyme histochemistryGeneral Medicinemedicine.diseaseImmunohistochemistryCongenital myopathyMuscle StriatedClinical methodEnzymesMicroscopy ElectronNeurologyNeurology (clinical)medicine.symptombusinessActa Neurologica Scandinavica
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The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Mod…

2012

BACKGROUND: In a previous work we showed for the first time that human tumor cells secrete Hsp60 via exosomes, which are considered immunologically active microvesicles involved in tumor progression. This finding raised questions concerning the route followed by Hsp60 to reach the exosomes, its location in them, and whether Hsp60 can be secreted also via other mechanisms, e.g., by the Golgi. We addressed these issues in the work presented here. PRINCIPAL FINDINGS: We found that Hsp60 localizes in the tumor cell plasma membrane, is associated with lipid rafts, and ends up in the exosomal membrane. We also found evidence that Hsp60 localizes in the Golgi apparatus and its secretion is prevent…

Cell Physiologyanimal structuresAnatomy and PhysiologyHistologylcsh:MedicineGolgi ApparatusBiologyExosomesBiochemistrysymbols.namesakeCytosolMembrane MicrodomainsDiagnostic MedicineCell Line TumorOrganelleMolecular Cell BiologyPathologyHumansSecretionlcsh:ScienceLipid raftBiologyhsp60 exosomeOrganellesMultidisciplinarylcsh:RfungiChaperonin 60Golgi apparatusMicrovesiclesCellular StructuresTransport proteinCell biologyProtein TransportMembrane proteinSubcellular OrganellesTumor progressionsymbolsCytochemistryMedicinelcsh:QMembranes and SortingExtracellular SpaceBiomarkersResearch ArticleGeneral PathologyPLoS ONE
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Binding properties of mechanically and enzymatically isolated hepatocytes for IgG and C3.

2008

— The presence of Fc and C3 receptors was studied on mechanically and enzymatically isolated rabbit, mouse and rat hepatocytes as well as on hepatocytes derived from primary cultures. The same cell preparations were used for studying the uptake of an antibody against nuclear antigens. Mechanically isolated hepatocytes were able to bind AIgG and activate complement. However, the same cells were not able to form rosettes with EA or with EAC. Enzymatically isolated hepatocytes did not bind AIgG or activate complement nor did they form rosettes with EA or with EAC. The mechanically isolated cells and the nonviable fraction of the enzymatically isolated cells showed a nuclear fluorescence when i…

Cell SurvivalImmunocytochemistryFc receptorFluorescent Antibody TechniqueCell SeparationReceptors FcMiceAntigenCell surface receptormedicineAnimalsHumansReceptorCells CulturedHepatologybiologyComplement C3Molecular biologyReceptors Complementmedicine.anatomical_structureBiochemistryLiverHepatocyteImmunoglobulin Gbiology.proteinRabbitsAntibodyIntracellularLiver
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Geographical mapping of metabolites in biological tissue with quantitative bioluminescence and single photon imaging

1993

This article features a novel technique for measuring the spatial distribution of metabolites, such as ATP, glucose, and lactate, in rapidly frozen tissue. Concentration values are obtained in absolute terms and with a spatial resolution of single-cell dimension. The method is based on enzymatic reactions that link the metabolite of interest to luciferase with subsequent light emission. Using a specific array, cryosections are brought into contact with the enzymes in a well-defined, reproducible way inducing a distribution of light across the section with an intensity that is proportional to the metabolite concentration. The emitted light can be visualized through a microscope and an imagin…

Cell SurvivalMetaboliteUterine Cervical NeoplasmsCarbohydrate metabolismBiologyMiceStructure-Activity Relationshipchemistry.chemical_compoundAdenosine TriphosphateNeoplasmsTumor Cells CulturedAnimalsFrozen SectionsHumansBioluminescenceTissue DistributionLuciferaseLactic AcidMelanomaCells Culturedchemistry.chemical_classificationMice Inbred BALB CStaining and LabelingHistocytochemistryMyocardiumCell BiologyPhoton countingRatsLactic acidGlucoseEnzymechemistryBiochemistryLuminescent MeasurementsLactatesBiophysicsFemaleLight emissionAnatomyThe Histochemical Journal
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Multiple sclerosis patient-derived CSF induces transcriptional changes in proliferating oligodendrocyte progenitors.

2014

Background: Cerebrospinal fluid (CSF) is in contact with brain parenchyma and ventricles, and its composition might influence the cellular physiology of oligodendrocyte progenitor cells (OPCs) thereby contributing to multiple sclerosis (MS) disease pathogenesis. Objective: To identify the transcriptional changes that distinguish the transcriptional response induced in proliferating rat OPCs upon exposure to CSF from primary progressive multiple sclerosis (PPMS) or relapsing remitting multiple sclerosis (RRMS) patients and other neurological controls. Methods: We performed gene microarray analysis of OPCs exposed to CSF from neurological controls, or definitive RRMS or PPMS disease course. R…

Cell physiologyAdultPathologymedicine.medical_specialtyTranscription GeneticGalectin 3GalectinsImmunocytochemistryBiologyArticleCerebrospinal fluidMultiple Sclerosis Relapsing-RemittingNeural Stem CellsmedicineAnimalsHumansProgenitor cellCells CulturedCell ProliferationCerebrospinal FluidMultiple sclerosisBrainHuman brainBlood ProteinsMultiple Sclerosis Chronic Progressivemedicine.diseaseMicroarray AnalysisNeural stem cellOligodendrocyteRatsUp-RegulationOligodendrogliamedicine.anatomical_structureNeurologyNeurology (clinical)Multiple sclerosis (Houndmills, Basingstoke, England)
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A Safe and Effective Magnetic Labeling Protocol for MRI-Based Tracking of Human Adult Neural Stem Cells

2019

Magnetic resonance imaging (MRI) provides a unique tool for in vivo visualization and tracking of stem cells in the brain. This is of particular importance when assessing safety of experimental cell treatments in the preclinical or clinical setup. Yet, specific imaging requires an efficient and non-perturbing cellular magnetic labeling which precludes adverse effects of the tag, e.g., the impact of iron-oxide-nanoparticles on the critical differentiation and integration processes of the respective stem cell population investigated. In this study we investigated the effects of very small superparamagnetic iron oxide particle (VSOP) labeling on viability, stemness, and neuronal differentiatio…

Cell physiologyImmunocytochemistryImaging phantomlcsh:RC321-57103 medical and health sciences0302 clinical medicineMedizinische FakultätIn vivomedicinemagnetic resonance imagingddc:610lcsh:Neurosciences. Biological psychiatry. NeuropsychiatryCNS – disorderOriginal Research030304 developmental biology0303 health sciencesmedicine.diagnostic_testChemistryQHGeneral Neurosciencemagnetic labelingCNS-disorderMagnetic resonance imagingVSOPR1Neural stem cellQRddc:Human Adult Stem Cells ; Magnetic Labeling ; Mri ; Cell Tracking ; Cns - DisorderCell biologycell trackingCNS – disorder ; human adult stem cells ; magnetic labeling ; MRI ; cell trackingStem cell030217 neurology & neurosurgeryNeuroscienceRChuman adult stem cellsMRIFrontiers in Neuroscience
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Immunohistochemical location of HPL, SP1 and β-HCG in normal placentas of varying gestational age

1986

Sixty-four placentas at various gestational ages were examined by immunohistochemical stains for HPL, SP1 and beta-HCG according to a modified PAP method (Sternberger 1970). Syncytiotrophoblast cell layer was identified as the main site of synthesis. Extravillous immunohistochemical reactions for HPL and SP1 (but not for beta-HCG) were found in X-cells of the basal plate and in the intervillous trophoblast islands. These cell types would thus seem to be derived from trophoblast. Hofbauer-cells of villous connective tissue stained specifically for beta-HCG apparently because of HCG phagocytosis. The intensity of staining for HPL, SP1 and beta-HCG was evaluated semiquantitatively in the syncy…

Cell typeTime FactorsPlacentaBasal plate (neural tube)Connective tissuePregnancy ProteinsBiologyChorionic GonadotropinImmunoenzyme TechniquesAndrologySyncytiotrophoblastPregnancymedicineHumansreproductive and urinary physiologyStaining and LabelingHistocytochemistryPregnancy-Specific beta 1-GlycoproteinsObstetrics and GynecologyGestational ageTrophoblastGeneral MedicinePlacental Lactogenfemale genital diseases and pregnancy complicationsTrophoblastsStainingmedicine.anatomical_structureembryonic structuresImmunologyImmunohistochemistryFemaleChorionic VilliArchives of Gynecology
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Dimethylsulfoxide as carrier in enzyme cytochemistry.

1971

Addition of dimethylsulfoxide (DMSO) to the incubation medium of succinate dehydrogenase in a concentration of 10% enhances the staining reaction in the hyphae of the fungus Cercosporella herpotrichoides after an incubation period of 15 min. Controls without DMSO remain unstained. DMSO causes a rapid penetration of the components of the medium through the mucilage that covers the hyphae.

CercosporellaHistologyintegumentary systembiologyHyphaStaining and LabelingHistocytochemistryorganic chemicalsSuccinate dehydrogenasefungiCell BiologyStainingIncubation periodMedical Laboratory TechnologyBiochemistryMucilagebiology.proteinCytochemistryDimethyl SulfoxideMitosporic FungiMolecular BiologyIncubationHistochemie. Histochemistry. Histochimie
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