| Literature DB >> 30057205 |
Chia-Yu Yeh1, Brent Asrican1, Jonathan Moss2, Luis Jhoan Quintanilla3, Ting He1, Xia Mao4, Frederic Cassé5, Elias Gebara2, Hechen Bao1, Wei Lu4, Nicolas Toni5, Juan Song6.
Abstract
Mossy cells (MCs) represent a major population of excitatory neurons in the adult dentate gyrus, a brain region where new neurons are generated from radial neural stem cells (rNSCs) throughout life. Little is known about the role of MCs in regulating rNSCs. Here we demonstrate that MC commissural projections structurally and functionally interact with rNSCs through both the direct glutamatergic MC-rNSC pathway and the indirect GABAergic MC-local interneuron-rNSC pathway. Specifically, moderate MC activation increases rNSC quiescence through the dominant indirect pathway, while high MC activation increases rNSC activation through the dominant direct pathway. In contrast, MC inhibition or ablation leads to a transient increase of rNSC activation, but rNSC depletion only occurs after chronic ablation of MCs. Together, our study identifies MCs as a critical stem cell niche component that dynamically controls adult NSC quiescence and maintenance under various MC activity states through a balance of direct glutamatergic and indirect GABAergic signaling onto rNSCs.Entities:
Keywords: adult hippocampal neurogenesis; maintenance; mossy cells; neural stem cells; quiescence
Mesh:
Year: 2018 PMID: 30057205 PMCID: PMC6092757 DOI: 10.1016/j.neuron.2018.07.010
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173