Proceedings of the National Academy of Sciences · 2019 · 12 citations · 32 references
Life SciencesNeurobiologyNeuroscienceCellular NeuroscienceDevelopmental NeuroscienceMolecular NeuroscienceNeural Circuit FormationNeural DevelopmentNeural Stem Cell BiologyNeural Stem CellsNeurogenesisNeuronal DevelopmentAdult Hippocampal NeurogenesisHippocampal PlasticityIntermediate Progenitor CellsNeural Stem Cell DifferentiationNeural Stem Cell MaintenanceNeural Stem Cell PlasticityProgenitor CellsSingle-cell Rna Sequencing
Adult hippocampal neurogenesis involves the lifelong generation of neurons. The process depends on the homeostasis of the production of neurons and maintenance of the adult neural stem cell (NSC) pool. Here, we report that α2-chimaerin, a Rho GTPase-activating protein, is essential for NSC homeostasis in adult hippocampal neurogenesis. Conditional deletion of α2-chimaerin in adult NSCs resulted in the premature differentiation of NSCs into intermediate progenitor cells (IPCs), which ultimately depleted the NSC pool and impaired neuron generation. Single-cell RNA sequencing and pseudotime analyses revealed that α2-chimaerin-conditional knockout (α2-CKO) mice lacked a unique NSC subpopulation, termed Klotho-expressing NSCs, during the transition of NSCs to IPCs. Furthermore, α2-CKO led to defects in hippocampal synaptic plasticity and anxiety/depression-like behaviors in mice. Our findings collectively demonstrate that α2-chimaerin plays an essential role in adult hippocampal NSC homeostasis to maintain proper brain function.
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Molecular Architecture of the Mouse Nervous System
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Medicine, Neurobiology, Neuroscience +14