Ascl1 (Mash1) Defines Cells with Long-Term Neurogenic Potential in Subgranular and Subventricular Zones in Adult Mouse Brain 英文参考文献.docVIP

Ascl1 (Mash1) Defines Cells with Long-Term Neurogenic Potential in Subgranular and Subventricular Zones in Adult Mouse Brain 英文参考文献.doc

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Ascl1 (Mash1) Defines Cells with Long-Term Neurogenic Potential in Subgranular and Subventricular Zones in Adult Mouse Brain 英文参考文献

Ascl1(Mash1)DefinesCellswithLong-TermNeurogenic PotentialinSubgranularandSubventricularZonesin AdultMouseBrain EuiseokJ.Kim1,JessicaL.Ables2,LaurenK.Dickel1,AmeliaJ.Eisch2,JaneE.Johnson1* 1DepartmentofNeuroscience,UniversityofTexasSouthwesternMedicalCenter,Dallas,Texas,UnitedStatesofAmerica,2DepartmentofPsychiatry,UniversityofTexas SouthwesternMedicalCenter,Dallas,Texas,UnitedStatesofAmerica Abstract Ascl1(Mash1)isabHLHtranscriptionfactoressentialforneuraldifferentiationduringembryogenesisbutitsroleinadult neurogenesisislessclear.HereweshowthatintheadultbrainAscl1isdynamicallyexpressedduringneurogenesisinthe dentategyrussubgranularzone(SGZ)andmorerostralsubventricularzone(SVZ).Specifically,wefindAscl1levelslowin SGZ Type-1 cells andSVZ B cells but increasing as thecells transition tointermediate progenitor stages. Invivo genetic lineage tracing with a tamoxifen (TAM) inducible Ascl1CreERT2 knock-in mouse strain shows that Ascl1 lineage cells continuously generate new neurons over extended periods of time. There is a regionally-specific difference in neuron generation,withmicegivenTAMatpostnatalday50showingnewdentategyrusneuronsthrough30dayspost-TAM,but showing new olfactory bulb neurons even 180 days post-TAM. These results show that Ascl1 is not restricted to transit amplifyingpopulationsbutisalsofoundinasubsetofneuralstemcellswithlong-termneurogenicpotentialintheadult brain. Citation: Kim EJ, Ables JL, Dickel LK, Eisch AJ, Johnson JE (2011) Ascl1 (Mash1) Defines Cells with Long-Term Neurogenic Potential in Subgranular and SubventricularZonesinAdultMouseBrain.PLoSONE6(3):e18472.doi:10.1371/journal.pone.0018472 Editor:AlainChe′dotal,InstitutdelaVision,France ReceivedJanuary12,2011;AcceptedMarch2,2011;PublishedMarch31,2011 Thisisanopen-accessarticle,freeofallcopyright,andmaybefreelyreproduced,distributed,transmitted,modified,builtupon,orotherwiseusedbyanyonefor anylawfulpurpose.TheworkismadeavailableundertheCreativeCommonsCC0publicdomaindedication. Funding:Thiswork

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