Search results for "Stem Cell"

showing 10 items of 2354 documents

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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Role of the cellular prion protein in oligodendrocyte precursor cell proliferation and differentiation in the developing and adult mouse CNS

2012

There are numerous studies describing the signaling mechanisms that mediate oligodendrocyte precursor cell (OPC) proliferation and differentiation, although the contribution of the cellular prion protein (PrP c) to this process remains unclear. PrP c is a glycosyl-phosphatidylinositol (GPI)-anchored glycoprotein involved in diverse cellular processes during the development and maturation of the mammalian central nervous system (CNS). Here we describe how PrP c influences oligodendrocyte proliferation in the developing and adult CNS. OPCs that lack PrP c proliferate more vigorously at the expense of a delay in differentiation, which correlates with changes in the expression of oligodendrocyt…

Central Nervous SystemTelencephalonMouseCellular differentiationanimal diseasesGene ExpressionHippocampusMice0302 clinical medicineNeural Stem CellsGene expressionMolecular Cell BiologyNeurobiology of Disease and RegenerationCell proliferationNeuronsCerebral CortexMice Knockout0303 health sciencesProliferació cel·lularMultidisciplinaryNeurogenesisQRCell DifferentiationAnimal ModelsNeural stem cell3. Good healthCell biologyOligodendrogliamedicine.anatomical_structureKnockout mouseMedicineFemaleBiologia del desenvolupamentCellular TypesCell DivisionResearch ArticlePrionsNeurogenesisScienceBiologyModels BiologicalCell Growth03 medical and health sciencesModel OrganismsDevelopmental NeuroscienceNeuroglial Developmentmental disordersDevelopmental biologymedicineAnimalsPrPC ProteinsBiology030304 developmental biologyCell ProliferationCell growthLineage markersMolecular DevelopmentOligodendrocytenervous system diseasesMice Inbred C57BLImmunologyOrganism Development030217 neurology & neurosurgeryDevelopmental BiologyNeuroscience
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Successive specification ofDrosophilaneuroblasts NB 6-4 and NB 7-3 depends on interaction of the segment polarity geneswingless,gooseberryandnaked cu…

2001

The Drosophila central nervous system derives from neural precursor cells, the neuroblasts (NBs), which are born from the neuroectoderm by the process of delamination. Each NB has a unique identity, which is revealed by the production of a characteristic cell lineage and a specific set of molecular markers it expresses. These NBs delaminate at different but reproducible time points during neurogenesis (S1-S5) and it has been shown for early delaminating NBs (S1/S2) that their identities depend on positional information conferred by segment polarity genes and dorsoventral patterning genes. We have studied mechanisms leading to the fate specification of a set of late delaminating neuroblasts,…

Central Nervous SystemTime FactorsCellular differentiationWnt1 ProteinBiologyCell fate determinationNeuroblastProto-Oncogene ProteinsAnimalsDrosophila ProteinsHedgehog ProteinsMolecular BiologyBody PatterningHomeodomain ProteinsNeuronsGeneticsNeuroectodermStem CellsNeurogenesisNuclear ProteinsCell DifferentiationengrailedCell biologyDNA-Binding ProteinsNaked cuticleDrosophila melanogasterSegment polarity geneembryonic structuresTrans-ActivatorsInsect ProteinsTranscription FactorsDevelopmental BiologyDevelopment
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Commitment of CNS Progenitors Along the Dorsoventral Axis of Drosophila Neuroectoderm

1995

In the Drosophila embryo, the central nervous system (CNS) develops from a population of neural stem cells (neuroblasts) and midline progenitor cells. Here, the fate and extent of determination of CNS progenitors along the dorsoventral axis was assayed. Dorsal neuroectodermal cells transplanted into the ventral neuroectoderm or into the midline produced CNS lineages consistent with their new position. However, ventral neuroectodermal cells and midline cells transplanted to dorsal sites of the neuroectoderm migrated ventrally and produced CNS lineages consistent with their origin. Thus, inductive signals at the ventral midline and adjacent neuroectoderm may confer ventral identities to CNS p…

Central Nervous SystemTransplantation Heterotopicanimal structuresCell TransplantationCentral nervous systemPopulationEctodermBiologyNeuroblastCell MovementEctodermmedicineAnimalsProgenitor celleducationNeuronseducation.field_of_studyMultidisciplinaryNeuroectodermStem CellsGastrulaAnatomyNeural stem cellCell biologyTransplantationmedicine.anatomical_structureMutationembryonic structuresDrosophilaNeurogliaStem Cell TransplantationScience
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Single cell cultures of Drosophila neuroectodermal and mesectodermal central nervous system progenitors reveal different degrees of developmental aut…

2009

Abstract Background The Drosophila embryonic central nervous system (CNS) develops from two sets of progenitor cells, neuroblasts and ventral midline progenitors, which behave differently in many respects. Neuroblasts derive from the neurogenic region of the ectoderm and form the lateral parts of the CNS. Ventral midline precursors are formed by two rows of mesectodermal cells and build the CNS midline. There is plenty of evidence that individual identities are conferred to precursor cells by positional information in the ectoderm. It is unclear, however, how far the precursors can maintain their identities and developmental properties in the absence of normal external signals. Results To s…

Central Nervous Systemanimal structuresEmbryo NonmammalianCentral nervous systemEctodermApoptosisBiologylcsh:RC346-429MesodermNeuroblastDevelopmental NeurosciencePrecursor cellmedicineAnimalsDrosophila ProteinsCell LineageProgenitor celllcsh:Neurology. Diseases of the nervous systemCells CulturedEmbryonic Stem CellsBody PatterningNeural PlatefungiCell DifferentiationEmbryonic stem cellmedicine.anatomical_structureCell cultureembryonic structuresDrosophilaNeuroscienceDevelopmental biologyCell DivisionResearch ArticleNeural development
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The origin of postembryonic neuroblasts in the ventral nerve cord of Drosophila melanogaster.

1991

ABSTRACT Embryonic and postembryonic neuroblasts in the thoracic ventral nerve cord of Drosophila melanogaster have the same origin. We have traced the development of threefold-labelled single precursor cells from the early gastrula stage to late larval stages. The technique allows in the same individual monitoring of progeny cells at embryonic stages (in vivo) and differentially staining embryonic and postembryonic progeny within the resulting neural clone at late postembryonic stages. The analysis reveals that postembryonic cells always appear together with embryonic cells in one clone. Further-more, BrdU labelling suggests that the embryonic neuroblast itself rather than one of its proge…

Central Nervous Systemanimal structuresNeurogenesisClone (cell biology)BiologyNeuroblastNeuroblasts/dk/atira/pure/subjectarea/asjc/2700/2702AnimalsBrdUMolecular BiologyCell lineageNeuroblast proliferationStem CellsfungiEmbryogenesisCell BiologyAnatomyGastrulaEmbryonic stem cellCell biologyGastrulationDrosophila melanogasterBromodeoxyuridineVentral nerve cordDrosophilaAnatomy/dk/atira/pure/subjectarea/asjc/1300/1307Ganglion mother cellDevelopmental BiologyDevelopment (Cambridge, England)
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Differential effects of EGF receptor signalling on neuroblast lineages along the dorsoventral axis of the Drosophila CNS

1998

ABSTRACT The Drosophila ventral nerve cord derives from a stereotype population of about 30 neural stem cells, the neuroblasts, per hemineuromere. Previous experiments provided indications for inductive signals at ventral sites of the neuroectoderm that confer neuroblast identities. Using cell lineage analysis, molecular markers and cell transplantation, we show here that EGF receptor signalling plays an instructive role in CNS patterning and exerts differential effects on dorsoventral subpopulations of neuroblasts. The Drosophila EGF receptor (DER) is capable of cell autonomously specifiying medial and intermediate neuroblast cell fates. DER signalling appears to be most critical for prope…

Central Nervous Systemanimal structuresPopulationCell fate determinationBiologyNeuroblastEctodermAnimalseducationReceptorMolecular BiologyBody PatterningNeuronseducation.field_of_studyNeuroectodermStem CellsfungiAnatomyNeural stem cellCell biologyErbB Receptorsnervous systemVentral nerve cordMutationembryonic structuresDrosophilaGanglion mother cellBiomarkersSignal TransductionStem Cell TransplantationDevelopmental BiologyDevelopment
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Stage-specific inductive signals in the Drosophila neuroectoderm control the temporal sequence of neuroblast specification.

2001

One of the initial steps of neurogenesis in the Drosophila embryo is the delamination of a stereotype set of neural progenitor cells (neuroblasts) from the neuroectoderm. The time window of neuroblast segregation has been divided into five successive waves (S1-S5) in which subsets of neuroblasts with specific identities are formed. To test when identity specification of the various neuroblasts takes place and whether extrinsic signals are involved, we have performed heterochronic transplantation experiments. Single neuroectodermal cells from stage 10 donor embryos (after S2) were transplanted into the neuroectoderm of host embryos at stage 7 (before S1) and vice versa. The fate of these cel…

Central Nervous Systemendocrine systemanimal structuresTime FactorsBiologyNeuroblastEctodermAnimalsProgenitor cellMolecular BiologyNeuronsNeuroectodermStem CellsfungiNeurogenesisEmbryoCell DifferentiationAnatomyNeural stem cellCell biologyTransplantationDrosophila melanogasternervous systemembryonic structuresGanglion mother cellDevelopmental BiologySignal TransductionDevelopment (Cambridge, England)
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Adult-derived neural precursors transplanted into multiple regions in the adult brain

1999

Neural stem cells persist in the adult brain subventricular zone (SVZ). These cells generate a large number of new neurons that migrate to the olfactory bulb, where they complete their differentiation. Here, we transplanted cells carrying beta-galactosidase under the control of neuron-specific enolase promoter (NSE::LacZ) from the SVZ of adult mice into the striatum cortex and olfactory bulb, with or without an excitotoxin lesion. Between 2 and 8 weeks after transplantation, grafted cells were present in the recipient regions, but extensive migration and differentiation into mature neurons of grafted cells were only observed in the olfactory bulb. Clusters of graft-derived neuroblasts formi…

Central nervous systemNeurogenesisSubventricular zoneBiologyNeural stem cellOlfactory bulbCell biologymedicine.anatomical_structurenervous systemNeurologyNeuroblastCerebral cortexmedicineNeurology (clinical)Olfactory ensheathing gliaNeuroscienceAnnals of Neurology
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Production of ceramides causes apoptosis during early neural differentiation in vitro.

2000

To investigate signal transduction pathways leading to apoptosis during the early phase of neurogenesis, we employed PCC7-Mz1 cells, which cease to proliferate and begin to differentiate into a stable pattern of neurons, astroglial cells, and fibroblasts upon incubation with retinoic acid (RA). As part of lineage determination, a sizable fraction of RA-treated cultures die by apoptosis. Applying natural long-chain C(16)-ceramides as well as membrane-permeable C(2)/C(6)-ceramide analogs caused apoptosis, whereas the biologically nonactive C(2)-dihydroceramide did not. Treating PCC7-Mz1 stem cells with a neutral sphingomyelinase or with the ceramidase inhibitor N-oleoylethanolamine elevated t…

CeramideCellular differentiationSerine C-PalmitoyltransferaseApoptosisOleic AcidsTretinoinBiologyCeramidesBiochemistryAmidohydrolasesCell Linechemistry.chemical_compoundMiceCeramidasesAnimalsCell LineageDrug InteractionsNerve TissueMolecular BiologyCeramide synthaseNeuronsStem CellsCell DifferentiationCell BiologyLipid signalingFibroblastsCeramidaseCell biologySphingomyelin PhosphodiesteraseBiochemistrychemistryApoptosisEthanolaminesAstrocytesSignal transductionSphingomyelinOxidoreductasesAcyltransferasesEndocannabinoidsSignal TransductionThe Journal of biological chemistry
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