Search results for "ganglio"

showing 10 items of 362 documents

Ganglioside GD3 shedding by human malignant melanoma cells

1989

Gangliosides appear to be important target molecules for immunological effector mechanisms on neuro-ectodermal tumors. Therefore in vitro studies were performed to examine whether ganglioside GD3, which is highly expressed on the cell surface of cultured human melanoma cells, is being shed into the culture medium. Measurable quantities of gangliosides GM3 and in particular GD3 were shed by the melanoma cells we have tested as detected on thin-layer chromatograms (TLC) stained with orcinol. Ganglioside GD3 was also evidenced by immunostaining with anti-GD3 MAb and by ELISA. The concentration of GD3 in the supernatant of human melanoma cells depended on the ganglioside pattern of the cell lin…

Cancer ResearchPathologymedicine.medical_specialtyGangliosideChemistryEffectormedicine.drug_classMelanomaCellmedicine.diseaseMonoclonal antibodyMolecular biologyIn vitromedicine.anatomical_structureOncologyCell cultureGangliosidesTumor Cells CulturedmedicineG(M3) GangliosideHumansGanglioside GD3lipids (amino acids peptides and proteins)MelanomaInternational Journal of Cancer
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Immunorecognition of different ganglioside epitopes on human normal and melanoma tissues.

1992

There is increasing evidence that cell-surface gangliosides play a role in tumor growth, progression and metastases. In order to determine the frequency of ganglioside GD3 in patients with metastatic malignant melanoma for further therapeutic trials, GD3 ganglioside expression was determined in 119 tissue samples. Of these melanomas, 93% (111/119) were R-24-positive, which indicates the value of this diagnostic marker for melanoma. To study the structural epitopes of gangliosides, 10 ganglioside antibodies with defined specificities and affinities were tested on over 100 fresh-frozen tissue specimens of human normal and melanoma tissues. All the antibodies tested recognize the ganglioside G…

Cancer ResearchPathologymedicine.medical_specialtySkin Neoplasmsmedicine.drug_classmedicine.medical_treatmentMonoclonal antibodyEpitopeEpitopesGangliosidesmedicineGanglioside GD3HumansNeoplasm MetastasisMelanomaGangliosidebiologyMelanomaAntibodies MonoclonalImmunotherapymedicine.diseaseMolecular biologyImmunohistochemistryOncologybiology.proteinImmunohistochemistrylipids (amino acids peptides and proteins)AntibodyInternational journal of cancer
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Prognostic value of International Neuroblastoma Pathology Classification in localized resectable peripheral neuroblastic tumors: a histopathologic st…

2006

Purpose To assess the prognostic value of clinical, biologic, and morphologic data in peripheral neuroblastic tumors, International Neuroblastoma Staging System (INSS) stages 2A and 2B MYCN nonamplified, a multinational protocol entitled Localized Neuroblastoma European Study Group trial 94.01, with a trial of surgery as the only treatment, was initiated in 1995. We present the prognostic value of the revised International Neuroblastoma Pathology Classification (INPC) applied to the patients included in this protocol until its closure in 1999. Materials and Methods A total of 120 neuroblastic tumors from trial patients were reviewed by the European International Society of Pediatric Oncolog…

Cancer Researchmedicine.medical_specialtyPathologyDisease-Free SurvivalNeuroblastomaPredictive Value of TestsNeuroblastomamedicineHumansSurvival analysisGanglioneuroblastomaL-Lactate Dehydrogenasebusiness.industryGanglioneuroblastomaAnatomical pathologymedicine.diseasePrognosisNeuroblastic TumorSurvival AnalysisClinical trialEuropeTreatment OutcomeOncologyPredictive value of testsHistopathologybusinessJournal of clinical oncology : official journal of the American Society of Clinical Oncology
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GD3 ganglioside: A marker for the diagnosis and treatment of neuroectodermal tumors?

1986

Cancer Researchmedicine.medical_specialtyPathologyGd3 gangliosideHematologyOncologybusiness.industryInternal medicinemedicineGeneral MedicinebusinessJournal of Cancer Research and Clinical Oncology
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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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Co-expression of the voltage-gated potassium channel Kv1.4 with transient receptor potential channels (TRPV1 and TRPV2) and the cannabinoid receptor …

2006

Potassium channels contribute to basic neuronal excitability and modulation. Here, we examined expression patterns of the voltage-gated potassium channel Kv1.4, the nociceptive transduction channels TRPV1 and TRPV2 as well as the putative anti-nociceptive cannabinoid receptor CB1 by immunofluorescence double-labelings in sections of rat dorsal root ganglia (DRGs). Kv1.4, TRPV1 and CB1 were each detected in about one third of neurons (35.7+/-0.5%, 29.4+/-1.1% and 36.4+/-0.5%, respectively, mean diameter 19.1+/-0.3 microm). TRPV2 was present in 4.4+/-0.4% of all neurons that were significantly larger in diameter (27.4+/-0.7 microm; P < 0.001). Antibody double-labeling revealed that the majori…

Cannabinoid receptorTRPV2Blotting WesternTRPV1TRPV Cation ChannelsCell CountRats Sprague-DawleyTransient receptor potential channelDorsal root ganglionReceptor Cannabinoid CB1Ganglia SpinalmedicineAnimalsCells CulturedIn Situ HybridizationNeuronsChemistrymusculoskeletal neural and ocular physiologyGeneral NeuroscienceVoltage-gated potassium channelMolecular biologyImmunohistochemistryPotassium channelSensory neuronRatsmedicine.anatomical_structureShal Potassium Channelsnervous systemlipids (amino acids peptides and proteins)Neurosciencepsychological phenomena and processesNeuroscience
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The Embryonic Central Nervous System Lineages ofDrosophila melanogaster

1996

In Drosophila, central nervous system (CNS) formation starts with the delamination from the neuroectoderm of about 30 neuroblasts (NBs) per hemisegment. They give rise to approximately 350 neurons and 30 glial cells during embryonic development. Understanding the mechanisms leading to cell fate specification and differentiation in the CNS requires the identification of the NB lineages. The embryonic lineages derived from 17 NBs of the ventral part of the neuroectoderm have previously been described (Bossing et al., 1996). Here we present 13 lineages derived from the dorsal part of the neuroectoderm and we assign 12 of them to identified NBs. Together, the 13 lineages comprise approximately …

Cell divisionNeuroectodermLineage (evolution)food and beveragesAnatomyCell BiologyBiologyCell fate determinationEmbryonic stem cellCell biologynervous systemNeuroblastVentral nerve cordembryonic structuresGanglion mother cellMolecular BiologyDevelopmental BiologyDevelopmental Biology
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Timing of identity: spatiotemporal regulation of hunchback in neuroblast lineages of Drosophila by Seven-up and Prospero.

2006

Neural stem cells often generate different cell types in a fixed birth order as a result of temporal specification of the progenitors. In Drosophila, the first temporal identity of most neural stem cells(neuroblasts) in the embryonic ventral nerve cord is specified by the transient expression of the transcription factor Hunchback. When reaching the next temporal identity, this expression is switched off in the neuroblasts by seven up (svp) in a mitosis-dependent manner, but is maintained in their progeny (ganglion mother cells). We show that svpmRNA is already expressed in the neuroblasts before this division. After mitosis, Svp protein accumulates in both cells, but the downregulation of h…

Cell typeReceptors Steroidanimal structuresTranscription GeneticMitosisNerve Tissue ProteinsNeuroblastAnimalsDrosophila ProteinsCell LineageProgenitor cellMolecular BiologyMitosisGeneticsNeuronsbiologyStem CellsfungiGene Expression Regulation DevelopmentalNuclear ProteinsProsperobiology.organism_classificationEmbryonic stem cellNeural stem cellCell biologyDNA-Binding ProteinsDrosophila melanogasterGanglion mother cellDevelopmental BiologyTranscription FactorsDevelopment (Cambridge, England)
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Neuroblast pattern and identity in the Drosophila tail region and role of doublesex in the survival of sex-specific precursors.

2013

The central nervous system is composed of segmental units (neuromeres), the size and complexity of which evolved in correspondence to their functional requirements. In Drosophila, neuromeres develop from populations of neural stem cells (neuroblasts) that delaminate from the early embryonic neuroectoderm in a stereotyped spatial and temporal pattern. Pattern units closely resemble the ground state and are rather invariant in thoracic (T1-T3) and anterior abdominal (A1-A7) segments of the embryonic ventral nerve cord. Here, we provide a comprehensive neuroblast map of the terminal abdominal neuromeres A8-A10, which exhibit a progressively derived character. Compared with thoracic and anterio…

Central Nervous SystemMaleanimal structuresDoublesexSerial homologyApoptosisBiologyNeuroblastNeural Stem CellsAbdomenImage Processing Computer-AssistedAnimalsDrosophila ProteinsCell LineageMolecular BiologyBody PatterningSex CharacteristicsMicroscopy ConfocalNeuroectodermAnatomyNeuromereImmunohistochemistryNeural stem cellCell biologyDNA-Binding ProteinsVentral nerve cordDrosophilaFemaleGanglion mother cellDevelopmental BiologyDevelopment (Cambridge, England)
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Programmed cell death in the embryonic central nervous system of Drosophila melanogaster.

2006

Although programmed cell death (PCD) plays a crucial role throughout Drosophila CNS development, its pattern and incidence remain largely uninvestigated. We provide here a detailed analysis of the occurrence of PCD in the embryonic ventral nerve cord (VNC). We traced the spatio-temporal pattern of PCD and compared the appearance of, and total cell numbers in,thoracic and abdominal neuromeres of wild-type and PCD-deficient H99mutant embryos. Furthermore, we have examined the clonal origin and fate of superfluous cells in H99 mutants by DiI labeling almost all neuroblasts, with special attention to segment-specific differences within the individually identified neuroblast lineages. Our data r…

Central Nervous SystemProgrammed cell deathanimal structuresEmbryo NonmammalianApoptosisCell CountBiologyNeuroblastInterneuronsmedicineAnimalsCell LineageMolecular BiologyBody PatterningNeuronsGene Expression Regulation DevelopmentalAnatomyNeuromerebiology.organism_classificationEmbryonic stem cellImmunohistochemistryCell biologyClone Cellsmedicine.anatomical_structureDrosophila melanogasternervous systemVentral nerve cordMutationNeuronDrosophila melanogasterGanglion mother cellDevelopmental BiologyDevelopment (Cambridge, England)
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