GABA regulates synaptic integration of newly generated neurons in the adult brain
Adult neurogenesis, the birth and integration of new neurons from adult neural stem cells, is a striking form of structural plasticity and highlights the regenerative capacity of the adult mammalian brain. Accumulating evidence suggests that neuronal activity regulates adult neurogenesis and that ne...
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Published in: | Nature Vol. 439; no. 7076; pp. 589 - 593 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
London
Nature Publishing
02-02-2006
Nature Publishing Group |
Subjects: | |
Online Access: | Get full text |
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Summary: | Adult neurogenesis, the birth and integration of new neurons from adult neural stem cells, is a striking form of structural plasticity and highlights the regenerative capacity of the adult mammalian brain. Accumulating evidence suggests that neuronal activity regulates adult neurogenesis and that new neurons contribute to specific brain functions. The mechanism that regulates the integration of newly generated neurons into the pre-existing functional circuitry in the adult brain is unknown. Here we show that newborn granule cells in the dentate gyrus of the adult hippocampus are tonically activated by ambient GABA (γ-aminobutyric acid) before being sequentially innervated by GABA- and glutamate-mediated synaptic inputs. GABA, the major inhibitory neurotransmitter in the adult brain, initially exerts an excitatory action on newborn neurons owing to their high cytoplasmic chloride ion content. Conversion of GABA-induced depolarization (excitation) into hyperpolarization (inhibition) in newborn neurons leads to marked defects in their synapse formation and dendritic development in vivo. Our study identifies an essential role for GABA in the synaptic integration of newly generated neurons in the adult brain, and suggests an unexpected mechanism for activity-dependent regulation of adult neurogenesis, in which newborn neurons may sense neuronal network activity through tonic and phasic GABA activation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 these authors contribute equally to this work. Author Contributions S-y. G did virus injection and electrophysiology, E.G. engineered retroviral constructs and did characterization, K.S. did immunohistochemistry and confocal imaging analysis, Y.K. helped with molecular biology, G-l. M. and H.S. are both senior authors and are responsible for project planning. All authors discussed the results and commented on the manuscript. Author Information Reprints and permissions information is available at npg.nature.com/reprintsandpermissions. The authors declare no competing financial interests. Correspondence and requests for materials should be addressed to H.S. (shongju1@bs.jhmi.edu.) or G-l. M. (gming1@bs.jhmi.edu.). |
ISSN: | 0028-0836 1476-4687 1476-4679 |
DOI: | 10.1038/nature04404 |