Search results for "Cell Division"

showing 10 items of 457 documents

Spot compliant neuronal networks by structure optimized micro-contact printing

2001

Neuronal cell growth in vitro can be controlled with micropatterned structures of extracellular matrix proteins such as laminin. This technique is a powerful tool for studying neuronal cell function in order to increase experimental reproducibility and to specifically design innovative experimental setups. In this paper the correlation between the structural dimensions of the ECM pattern and the shape of the resulting cellular network is analyzed. The aim of the present study was to position neuronal cell bodies as precisely as possible and to induce directed cell differentiation. PCC7-MzN cells were cultured on laminin patterns. The line width, node size and gap size in-between cell adhesi…

Cellular differentiationBiophysicsBioengineeringNanotechnologyBiologyMicrographyBiomaterialsExtracellular matrixMiceLamininTumor Cells CulturedAnimalsCell adhesionNeuronsExtracellular Matrix ProteinsCell growthReproducibility of ResultsCell DifferentiationMicroscopy FluorescenceMechanics of MaterialsMicrocontact printingCeramics and Compositesbiology.proteinNeural Networks ComputerNODALCell DivisionBiomedical engineeringBiomaterials
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EGF converts transit-amplifying neurogenic precursors in the adult brain into multipotent stem cells.

2002

AbstractNeural stem cells in the subventricular zone (SVZ) continue to generate new neurons in the adult brain. SVZ cells exposed to EGF in culture grow to form neurospheres that are multipotent and self-renewing. We show here that the majority of these EGF-responsive cells are not derived from relatively quiescent stem cells in vivo, but from the highly mitotic, Dlx2+, transit-amplifying C cells. When exposed to EGF, C cells downregulate Dlx2, arrest neuronal production, and become highly proliferative and invasive. Killing Dlx2+ cells dramatically reduces the in vivo response to EGF and neurosphere formation in vitro. Furthermore, purified C cells are 53-fold enriched for neurosphere gene…

Cellular differentiationNeuroscience(all)Mice TransgenicBiology03 medical and health sciencesMice0302 clinical medicineCell MovementNeurosphereSpheroids CellularAnimalsCell LineageCells Cultured030304 developmental biologyHomeodomain ProteinsNeurons0303 health sciencesEpidermal Growth FactorGeneral NeuroscienceStem CellsBrainCell DifferentiationImmunohistochemistryNeural stem cellCell biologyUp-RegulationNeuroepithelial cellEndothelial stem cellErbB ReceptorsMicroscopy ElectronPhenotypenervous systemMultipotent Stem CellAstrocytesStem cellNeuroscience030217 neurology & neurosurgeryCell DivisionAdult stem cellTranscription FactorsNeuron
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Extramedullary Expansion of Hematopoietic Progenitor Cells in Interleukin (IL)-6–sIL-6R Double Transgenic Mice

1997

Soluble cytokine receptors modulate the activity of their cognate ligands. Interleukin (IL)-6 in association with the soluble IL-6 receptor (sIL-6R) can activate cells expressing the gp130 signal transducer lacking the specific IL-6R. To investigate the function of the IL-6–sIL-6R complex in vivo and to discriminate the function of the IL-6–sIL-6R complex from the function of IL-6 alone, we have established a transgenic mouse model. Double-transgenic mice coexpressing IL-6 and sIL-6R were generated and compared with IL-6 and sIL-6R single-transgenic mice. The main phenotype found in IL-6–sIL-6R mice was a dramatic increase of extramedullary hematopoietic progenitor cells in liver and spleen…

Cellular differentiationmedicine.medical_treatmentImmunologyMice TransgenicCell SeparationBiologyArticleMiceAntigens CDCytokine Receptor gp130medicineAnimalsHumansImmunology and AllergyPeripheral blood cellInterleukin 6Interleukin 3Membrane GlycoproteinsInterleukin-6Body WeightInterleukinCell DifferentiationArticlesOrgan SizeFlow CytometryHematopoietic Stem CellsGlycoprotein 130ImmunohistochemistryMolecular biologyCell biologymedicine.anatomical_structureCytokineLiverbiology.proteinBone marrowCell DivisionSpleenSignal TransductionJournal of Experimental Medicine
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Thymidine analogs are transferred from prelabeled donor to host cells in the central nervous system after transplantation: a word of caution

2006

Thymidine analogs, including bromodeoxyuridine, chlorodeoxyuridine, iododeoxyuridine, and tritiated thymidine, label dividing cells by incorporating into DNA during S phase of cell division and are widely employed to identify cells transplanted into the central nervous system. However, the potential for transfer of thymidine analogs from grafted cells to dividing host cells has not been thoroughly tested. We here demonstrate that graft-derived thymidine analogs can become incorporated into host neural precursors and glia. Large numbers of labeled neurons and glia were found 3-12 weeks after transplantation of thymidine analog-labeled live stem cells, suggesting differentiation of grafted ce…

Central Nervous SystemCell divisionCentral nervous systemBiological Transport ActiveMice TransgenicIn Vitro TechniquesBiologyRats Sprague-Dawleychemistry.chemical_compoundMicePregnancyRats Inbred SHRmedicineAnimalsCell ProliferationNeuronsCell growthBrainCell BiologyMolecular biologyRatsTransplantationmedicine.anatomical_structurechemistryAnimals NewbornBromodeoxyuridineMolecular MedicineNeurogliaFemaleStem cellThymidineNeurogliaBromodeoxyuridineDevelopmental BiologyStem Cell TransplantationThymidine
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Single cell transplantation reveals interspecific cell communication in Drosophila chimeras

1990

Abstract Cell –cell communication is not only a common strategy for cell fate specification in vertebrates, but plays important roles in invertebrate development as well. We report here on experiments testing the compatibility of mechanisms specifying cell fate among six different Drosophila species. Following interspecific transplantation, the development of single ectodermal cells was traced in order to test their abilities to proliferate and differentiate in a heterologous environment. Despite considerable differences in cell size and length of cell cycle among some of the species, the transplants gave rise to fully differentiated clones that were integrated into the host tissue. Clones …

Central Nervous SystemCell signalingChimeraHeterologousCell DifferentiationEctodermCell CommunicationAnatomyInterspecific competitionCell cycleBiologyCell fate determinationClone CellsCell biologyTransplantationMicroscopy Electronmedicine.anatomical_structureCell transplantationEctodermmedicineAnimalsDrosophilaMolecular BiologyCell DivisionDevelopmental BiologyDevelopment
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A critical role for Cyclin E in cell fate determination in the central nervous system of Drosophila melanogaster

2004

We have examined the process by which cell diversity is generated in neuroblast (NB) lineages in the central nervous system of Drosophila melanogaster. Thoracic NB6-4 (NB6-4t) generates both neurons and glial cells, whereas NB6-4a generates only glial cells in abdominal segments. This is attributed to an asymmetric first division of NB6-4t, localizing prospero (pros) and glial cell missing (gcm) only to the glial precursor cell, and a symmetric division of NB6-4a, where both daughter cells express pros and gcm. Here we show that the NB6-4t lineage represents the ground state, which does not require the input of any homeotic gene, whereas the NB6-4a lineage is specified by the homeotic genes…

Central Nervous SystemCyclin ELineage (genetic)Cell divisionDown-RegulationNerve Tissue ProteinsCell fate determinationNeuroblastCyclin EAnimalsDrosophila ProteinsCell LineageHomeodomain ProteinsNeuronsbiologyStem CellsNeuropeptidesGenes HomeoboxGene Expression Regulation DevelopmentalNuclear ProteinsCell DifferentiationCell BiologyCell cyclebiology.organism_classificationGanglia InvertebrateCell biologyDNA-Binding ProteinsDrosophila melanogasterTrans-ActivatorsDrosophila melanogasterHomeotic geneNeurogliaTranscription FactorsNature Cell Biology
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Oligodendrogliogenic and neurogenic adult subependymal zone neural stem cells constitute distinct lineages and exhibit differential responsiveness to…

2012

The adult mouse subependymal zone (SEZ) harbours adult neural stem cells (aNSCs) that give rise to neuronal and oligodendroglial progeny. However it is not known whether the same aNSC can give rise to neuronal and oligodendroglial progeny or whether these distinct progenies constitute entirely separate lineages. Continuous live imaging and single-cell tracking of aNSCs and their progeny isolated from the mouse SEZ revealed that aNSCs exclusively generate oligodendroglia or neurons, but never both within a single lineage. Moreover, activation of canonical Wnt signalling selectively stimulated proliferation within the oligodendrogliogenic lineage, resulting in a massive increase in oligodendr…

Central Nervous SystemMaleReceptor Platelet-Derived Growth Factor alphaWnt signallingNerve Tissue ProteinsBiologyWnt3 ProteinMiceNeural Stem CellsLive cell imagingSubependymal zoneBasic Helix-Loop-Helix Transcription FactorsAnimalsCell LineageWnt Signaling PathwayCells CulturedProgenitorCell ProliferationCell CycleWnt signaling pathwayCell DifferentiationCell BiologyOligodendrocyte Transcription Factor 2Neural stem cellCell biologyMice Inbred C57BLOligodendrogliaFemaleCell DivisionNature cell biology
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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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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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Delayed postnatal neurogenesis in the cerebral cortex of lizards

1988

Labelled cells were consistently observed in the medial cortex of the lizard brain after i.p. injections of tritiated thymidine (5 microCi/g b. wt.), 1, 7, 18 or 28 days of survival and posterior autoradiographic evaluation. In 3 groups of specimens (postnatal, young and adult) of the species Podarcis hispanica, after one day of survival, labelled cells were located in the ependymal cell layer underlying the medial cortex. After intermediate survival times (7, 18 days), labelled cells were found in 3 zones: the ependymal layer, the inner plexiform layer and the granular layer. After one month of survival, most labelled cells were observed in the granular layer. In the granular layer, these …

Cerebral CortexEpendymal CellMedial cortexHippocampusLizardsAnatomyGranular layerBiologyInner plexiform layerbiology.organism_classificationPodarcis hispanicaMicroscopy Electronmedicine.anatomical_structureDevelopmental NeuroscienceCerebral cortexmedicineAnimalsAutoradiographyFascia dentataCell DivisionThymidineDevelopmental BiologyDevelopmental Brain Research
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