Search results for "neuroblast"

showing 10 items of 348 documents

Analysis of Drosophila salivary gland, epidermis and CNS development suggests an additional function of brinker in anterior-posterior cell fate speci…

2000

Salivary glands are simple structured organs which can serve as a model system in the study of organogenesis. Following a large EMS mutagenesis we have identified a number of genes required for normal salivary gland development. Mutations in the locus small salivary glands-1 (ssg-1) lead to a drastic reduction in the size of the salivary glands. The gene ssg-1 was cloned and subsequent sequence and genetic analysis showed identity to the recently published gene brinker. The salivary gland placode in brinker mutants appears reduced along both the anterior-posterior and dorso-ventral axis. Analysis of the brinker cuticle phenotype revealed a similar loss of anterior-posterior as well as later…

Central Nervous SystemEmbryologyReceptors SteroidEmbryo NonmammalianMutantLocus (genetics)OrganogenesisBiologyCell fate determinationSalivary GlandsNeuroblastBacterial ProteinsmedicineAnimalsDrosophila ProteinsAdhesins BacterialGeneBody PatterningEmbryonic InductionHomeodomain ProteinsSalivary glandGenetic Complementation TestNeuropeptidesChromosome MappingGene Expression Regulation DevelopmentalCell DifferentiationAnatomyPhenotypeCell biologyRepressor Proteinsmedicine.anatomical_structureEpidermal CellsMutationInsect ProteinsDrosophilaEpidermisDevelopmental BiologyTranscription FactorsMechanisms of development
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Impact of Ultrabithorax alternative splicing on Drosophila embryonic nervous system development.

2015

Hox genes control divergent segment identities along the anteroposterior body axis of bilateral animals by regulating a large number of processes in a cell context-specific manner. How Hox proteins achieve this functional diversity is a long-standing question in developmental biology. In this study we investigate the role of alternative splicing in functional specificity of the Drosophila Hox gene Ultrabithorax (Ubx). We focus specifically on the embryonic central nervous system (CNS) and provide a description of temporal expression patterns of three major Ubx isoforms during development of this tissue. These analyses imply distinct functions for individual isoforms in different stages of n…

Central Nervous SystemEmbryologyanimal structuresNeurogenesisGenes InsectBiologyCell fate determinationNeuroblastAnimalsDrosophila ProteinsProtein IsoformsHox geneUltrabithoraxGeneticsHomeodomain ProteinsAlternative splicingGenes HomeoboxGene Expression Regulation DevelopmentalCell biologyAlternative Splicingembryonic structuresRNA splicingDrosophilaNeural developmentDrosophila ProteinDevelopmental BiologyTranscription FactorsMechanisms of development
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Immunoproteomic studies on paediatric opsoclonus-myoclonus associated with neuroblastoma

2016

We aimed to identify new cell-membrane antigens implicated in opsoclonus-myoclonus with neuroblastoma. The sera of 3 out of 14 patients showed IgG electron-microscopy immunogold reactivity on SH-SY5Y neuroblastoma cells. Immunoprecipitation experiments using rat brain synaptosomes and SH-SY5Y cells led to the identification of: (1) thirty-one nuclear/cytoplasmic proteins (including antigens HuB, HuC); (2) seven neuronal membrane proteins, including the Shaw-potassium channel Kv3.3 (KCNC3), whose genetic disruption in mice causes ataxia and generalized muscle twitching. Although cell-based assays did not demonstrate direct antigenicity, our findings point to Shaw-related subfamily of the pot…

Central Nervous SystemMale0301 basic medicineAntigenicityDatabases FactualThymomaImmunoprecipitationKCTD7Cell Adhesion Molecules NeuronalImmunologyNerve Tissue ProteinsBiologyNeuroblastoma03 medical and health sciences0302 clinical medicineAntigenCell Line TumorNeuroblastomaOpsoclonus myoclonus syndromemedicineAnimalsHumansImmunology and AllergyRats WistarChildOpsoclonus-Myoclonus SyndromeBrain NeoplasmsMembrane ProteinsNuclear ProteinsImmunogold labellingmedicine.diseaseMolecular biologyRatsHEK293 Cells030104 developmental biologyShaw Potassium ChannelsNeurologyMembrane proteinEncephalitisFemaleNeurology (clinical)030217 neurology & neurosurgerySynaptosomesJournal of Neuroimmunology
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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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The commonly used marker ELAV is transiently expressed in neuroblasts and glial cells in theDrosophilaembryonic CNS

2007

Glial cells in the Drosophila embryonic nervous system can be monitored with the marker Reversed-polarity (Repo), whereas neurons lack Repo and express the RNA-binding protein ELAV (Embryonic Lethal, Abnormal Vision). Since the first description of the ELAV protein distribution in 1991 (Robinow and White), it is believed that ELAV is an exclusive neuronal and postmitotic marker. Looking at ELAV expression, we unexpectedly observed that, in addition to neurons, ELAV is transiently expressed in embryonic glial cells. Furthermore, it is transiently present in the proliferating longitudinal glioblast, and it is transcribed in embryonic neuroblasts. Likewise, elav-Gal4 lines, which are generally…

Central Nervous SystemNervous systemGenes InsectBiologyAnimals Genetically ModifiedGlioblastNeuroblastGenes ReportermedicineAnimalsDrosophila ProteinsEmbryonic Stem CellsNeuronsRegulation of gene expressionGene Expression Regulation DevelopmentalEmbryoAnatomyEmbryonic stem cellPhenotypeNeural stem cellCell biologyPhenotypemedicine.anatomical_structureELAV Proteinsnervous systemMutationDrosophilaNeurogliaDevelopmental BiologyDevelopmental Dynamics
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A common precursor for glia and neurons in the embryonic CNS of Drosophila gives rise to segment-specific lineage variants

1993

ABSTRACT The nervous system consists of two classes of cells, neurons and glia, which differ in morphology and function. They derive from precursors located in the neurogenic region of the ectoderm. In this study, we present the complete embryonic lineage of a neuroectodermal precursor in Drosophila that gives rise to neurons as well as glia in the abdominal CNS. This lineage is conserved among different Drosophila species. We show that neuronal and glial cell types in this clone derive from one segregating precursor, previously described as NB1-1. Thus, in addition to neuroblasts and glioblasts, there exists a third class of CNS precursors in Drosophila, which we call neuroglioblasts. We f…

Central Nervous SystemNervous systemanimal structuresLineage (genetic)Cell TransplantationCellular differentiationEctodermBiologySpecies SpecificityNeuroblastCell MovementAbdomenEctodermMorphogenesismedicineAnimalsMolecular BiologyHorseradish PeroxidaseNeuronsStem CellsCell DifferentiationGastrulaAnatomyCarbocyaninesThoraxCell biologyTransplantationDrosophila melanogastermedicine.anatomical_structurenervous systemNeurogliaDrosophilaNeuronNeurogliaDevelopmental BiologyDevelopment
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Hunchback is required for the specification of the early sublineage of neuroblast 7-3 in the Drosophila central nervous system.

2002

The Drosophila ventral nerve cord (VNC) derives from neuroblasts (NBs), which mostly divide in a stem cell mode and give rise to defined NB lineages characterized by specific sets of sequentially generated neurons and/or glia cells. To understand how different cell types are generated within a NB lineage, we have focused on the NB7-3 lineage as a model system. This NB gives rise to four individually identifiable neurons and we show that these cells are generated from three different ganglion mother cells (GMCs). The finding that the transcription factor Hunchback (Hb) is expressed in the early sublineage of NB7-3, which consists of the early NB and the first GMC (GMC7-3a) and its progeny (E…

Central Nervous SystemNeuronsCell typeLineage (genetic)biologyStem CellsGene ExpressionAnatomyCell fate determinationbiology.organism_classificationCell biologyDNA-Binding ProteinsDrosophila melanogasterNeuroblastMutagenesisVentral nerve cordAnimalsDrosophila ProteinsCell LineageStem cellDrosophila melanogasterMolecular BiologyDrosophila ProteinDevelopmental BiologyTranscription FactorsDevelopment (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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Human neuroblastoma SH-SY5Y cell line: neurosteroid-producing cell line relying on cytoskeletal organization.

2000

Pregnenolone, the precursor of all steroids, is synthesized by CNS structures. The synthesis requires an obligatory step involving cholesterol transport to mitochondrial cytochrome P450-cholesterol side chain cleavage (cytP450scc), although the underlying mechanism(s) are still mostly unknown. We used the human neuroblastoma SH-SY5Y cell line to investigate cytP450scc expression and activity and to establish a role of cytoskeleton in pregnenolone synthesis. Immunocytochemical and biochemical approaches revealed that undifferentiated as well as differentiated cells either by retinoic acid (RA) or phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA), possess cytP450scc and rapidly synthes…

Central Nervous SystemSH-SY5YNeuroactive steroidCellular differentiationRetinoic acidTrilostaneBiologyCellular and Molecular Neurosciencechemistry.chemical_compoundNeuroblastomachemistryBiochemistryCytochrome P-450 Enzyme SystemCell culturePregnenolonemedicinePregnenoloneTumor Cells CulturedHumansSteroidsCholesterol Side-Chain Cleavage EnzymeCytoskeletonCytoskeletonmedicine.drugJournal of neuroscience research
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Abdominal-B and caudal inhibit the formation of specific neuroblasts in the Drosophila tail region

2013

The central nervous system of Drosophila melanogaster consists of fused segmental units (neuromeres), each generated by a characteristic number of neural stem cells (neuroblasts). In the embryo, thoracic and anterior abdominal neuromeres are almost equally sized and formed by repetitive sets of neuroblasts, whereas the terminal abdominal neuromeres are generated by significantly smaller populations of progenitor cells. Here we investigated the role of the Hox gene Abdominal-B in shaping the terminal neuromeres. We show that the regulatory isoform of Abdominal-B (Abd-B.r) not only confers abdominal fate to specific neuroblasts (e.g. NB6-4) and regulates programmed cell death of several proge…

Central Nervous SystemTailanimal structuresCNS developmentCellular differentiationParaHoxApoptosisBiologyTerminal neuromeresAbdominal-BHox genesNeural Stem CellsNeuroblastNeuroblastsImage Processing Computer-AssistedAnimalsDrosophila ProteinsHox geneMolecular BiologyIn Situ HybridizationDNA PrimersHomeodomain ProteinsfungiCell DifferentiationStem Cells and RegenerationNeuromereImmunohistochemistryMolecular biologyNeural stem cellSegmental patterningDrosophila melanogasterMicroscopy Fluorescencenervous systemembryonic structuresCaudalDrosophilaGanglion mother cellDrosophila ProteinTranscription FactorsDevelopmental BiologyDevelopment
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