Nitric oxide negatively regulates mammalian adult neurogenesis

被引:249
作者
Packer, MA
Stasiv, Y
Benraiss, A
Chmielnicki, E
Grinberg, A
Westphal, H
Goldman, SA
Enikolopov, G
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] Cornell Univ, Coll Med, Dept Neurol & Neurosci, New York, NY 10021 USA
[3] NICHHD, Lab Mammalian Genes & Dev, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.1633579100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neural progenitor cells are widespread throughout the adult central nervous system but only give rise to neurons in specific loci. Negative regulators of neurogenesis have therefore been postulated, but none have yet been identified as subserving a significant role in the adult brain. Here we report that nitric oxide (NO) acts as an important negative regulator of cell proliferation in the adult mammalian brain. We used two independent approaches to examine the function of NO in adult neurogenesis. In a pharmacological approach, we suppressed NO production in the rat brain by intraventricular infusion of an NO synthase inhibitor. In a genetic approach, we generated a null mutant neuronal NO synthase knockout mouse line by targeting the exon encoding active center of the enzyme. In both models, the number of new cells generated in neurogenic areas of the adult brain, the olfactory subependyma and the dentate gyrus, was strongly augmented, which indicates that division of neural stem cells in the adult brain is controlled by NO and suggests a strategy for enhancing neurogenesis in the adult central nervous system.
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收藏
页码:9566 / 9571
页数:6
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