2019
Minimally Invasive Delivery of Microbeads with Encapsulated, Viable and Quiescent Neural Stem Cells to the Adult Subventricular Zone
Matta R, Lee S, Genet N, Hirschi KK, Thomas JL, Gonzalez AL. Minimally Invasive Delivery of Microbeads with Encapsulated, Viable and Quiescent Neural Stem Cells to the Adult Subventricular Zone. Scientific Reports 2019, 9: 17798. PMID: 31780709, PMCID: PMC6882840, DOI: 10.1038/s41598-019-54167-1.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsCell DifferentiationCell EncapsulationCell LineCell ProliferationCell SurvivalEndothelial CellsLateral VentriclesMaleMatrix MetalloproteinasesMiceMice, Inbred C57BLMicrospheresNeural Stem CellsNeuronsPolyethylene GlycolsRecovery of FunctionStem Cell NicheStem Cell TransplantationConceptsEndothelial cellsSubventricular zoneNSC quiescenceNon-injury modelQuiescent neural stem cellsAdult subventricular zoneNeuronal stem cellsStem cellsNeural stem cellsFunctional recoveryNeurological injuryInflammatory responseNeural stem cell maintenanceNSC deliveryNeural tissue repairNeurological diseasesMouse brainCell therapyNSC viabilityBrainTissue repairInjuryCo-encapsulated cellsSurvivalDelivery
2015
Embryonic Stem Cells License a High Level of Dormant Origins to Protect the Genome against Replication Stress
Ge XQ, Han J, Cheng EC, Yamaguchi S, Shima N, Thomas JL, Lin H. Embryonic Stem Cells License a High Level of Dormant Origins to Protect the Genome against Replication Stress. Stem Cell Reports 2015, 5: 185-194. PMID: 26190528, PMCID: PMC4618655, DOI: 10.1016/j.stemcr.2015.06.002.Peer-Reviewed Original ResearchConceptsEmbryonic stem cellsStem/progenitor cellsNeural stem/progenitor cellsStem cellsProgenitor cellsTissue stem/progenitor cellsMCM2-7 complexDNA replication originsTissue-specific stem/progenitor cellsStem cell typesGenome integrityGenomic integrityReplication stressDormant originsReplication forksReplicative stressDNA replicationReplication originsNeural lineagesDNA damageS phaseCell typesAbnormal neurogenesisCellsGenome
2002
Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1
Spassky N, de Castro F, Le Bras B, Heydon K, Quéraud-LeSaux F, Bloch-Gallego E, Chédotal A, Zalc B, Thomas J. Directional Guidance of Oligodendroglial Migration by Class 3 Semaphorins and Netrin-1. Journal Of Neuroscience 2002, 22: 5992-6004. PMID: 12122061, PMCID: PMC6757938, DOI: 10.1523/jneurosci.22-14-05992.2002.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsCell Adhesion MoleculesCell DivisionCell LineCell LineageCell MovementChemotaxisCulture TechniquesDCC ReceptorGlycoproteinsHumansMembrane ProteinsMiceNerve Growth FactorsNerve Tissue ProteinsNetrin ReceptorsNetrin-1Neuropilin-1OligodendrogliaOptic NerveReceptors, Cell SurfaceSemaphorin-3AStem CellsTumor Suppressor ProteinsConceptsOligodendrocyte precursor cellsEmbryonic optic nerveMigration of OPCsOptic nerveNetrin-1Sema 3ANetrin-1 receptorWhite matter tractsSema 3FMyelin-forming cellsColorectal cancerClass 3 semaphorinsLocalization of cellsNerveChemotactic effectNeuropilin-1Multiple fociFunctional migrationPrecursor cellsNetrin familyOligodendroglial migrationSemaphorinsNeural tubeDual effectGuidance cues
1996
Myelin/oligodendrocyte glycoprotein (MOG) expression is associated with myelin deposition
Solly S, Thomas J, Monge M, Demerens C, Lubetzki C, Gardinier M, Matthieu J, Zalc B. Myelin/oligodendrocyte glycoprotein (MOG) expression is associated with myelin deposition. Glia 1996, 18: 39-48. PMID: 8891690, DOI: 10.1002/(sici)1098-1136(199609)18:1<39::aid-glia4>3.0.co;2-z.Peer-Reviewed Original Research