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RESEARCH PRODUCT

Single-cell analysis of the ventricular-subventricular zone reveals signatures of dorsal and ventral adult neurogenesis

David M. WuBenjamin ManskyKirsten ObernierMarcos Assis NascimentoDaniel A. LimJosé Manuel García-verdugoArantxa Cebrián-sillaArturo Alvarez-buyllaSusana González-graneroRicardo Romero RodriguezStephanie A. Redmond

subject

MaleNervous systemMouseTransgenicneuroscienceMiceNeural Stem CellsLateral VentriclesBiology (General)education.field_of_studyGeneral NeuroscienceNeurogenesisQRGeneral MedicineStem Cells and Regenerative Medicineadult neurogenesismedicine.anatomical_structureolfactory bulbNeurologicalMedicineStem Cell Research - Nonembryonic - Non-HumanFemaleSingle-Cell AnalysisStem cellMicrodissectionneuroblastResearch ArticleQH301-705.51.1 Normal biological development and functioningNeurogenesisSciencePopulationregenerative medicineSubventricular zoneMice TransgenicBiologysingle-cell sequencingGeneral Biochemistry Genetics and Molecular BiologyNeuroblaststem cellsUnderpinning researchGeneticsmedicineAnimalseducationmouseGeneral Immunology and MicrobiologyNeurosciencesStem Cell ResearchOlfactory bulbstem cellnervous systemBiochemistry and Cell BiologyNeuronTranscriptomeNeuroscienceNeuroscienceregional differences

description

The ventricular-subventricular zone (V-SVZ), on the walls of the lateral ventricles, harbors the largest neurogenic niche in the adult mouse brain. Previous work has shown that neural stem/progenitor cells (NSPCs) in different locations within the V-SVZ produce different subtypes of new neurons for the olfactory bulb. The molecular signatures that underlie this regional heterogeneity remain largely unknown. Here, we present a single-cell RNA-sequencing dataset of the adult mouse V-SVZ revealing two populations of NSPCs that reside in largely non-overlapping domains in either the dorsal or ventral V-SVZ. These regional differences in gene expression were further validated using a single-nucleus RNA-sequencing reference dataset of regionally microdissected domains of the V-SVZ and by immunocytochemistry and RNAscope localization. We also identify two subpopulations of young neurons that have gene expression profiles consistent with a dorsal or ventral origin. Interestingly, a subset of genes are dynamically expressed, but maintained, in the ventral or dorsal lineages. The study provides novel markers and territories to understand the region-specific regulation of adult neurogenesis.

10.7554/elife.67436https://elifesciences.org/articles/67436