Activity-dependent PSA expression regulates inhibitory maturation and onset of critical period plasticity

被引:159
作者
Di Cristo, Graziella
Chattopadhyaya, Bidisha
Kuhlman, Sandra J.
Fu, Yu
Belanger, Marie-Claude
Wu, Cai Zhi
Rutishauser, Urs
Maffei, Lamberto
Huang, Z. Josh
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11734 USA
[2] SUNY Stony Brook, Neurosci Program, Stony Brook, NY 11790 USA
[3] Univ Montreal, CHU St Justine, Montreal, PQ H3T 1C5, Canada
[4] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[5] Inst Neuro Fisiol Ctr Nazl Ricerca, I-56124 Pisa, Italy
关键词
D O I
10.1038/nn2008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Functional maturation of GABAergic innervation in the developing visual cortex is regulated by neural activity and sensory inputs and in turn influences the critical period of ocular dominance plasticity. Here we show that polysialic acid (PSA), presented by the neural cell adhesion molecule, has a role in the maturation of GABAergic innervation and ocular dominance plasticity. Concentrations of PSA significantly decline shortly after eye opening in the adolescent mouse visual cortex; this decline is hindered by visual deprivation. The developmental and activity-dependent regulation of PSA expression is inversely correlated with the maturation of GABAergic innervation. Premature removal of PSA in visual cortex results in precocious maturation of perisomatic innervation by basket interneurons, enhanced inhibitory synaptic transmission, and earlier onset of ocular dominance plasticity. The developmental and activity-dependent decline of PSA expression therefore regulates the timing of the maturation of GABAergic inhibition and the onset of ocular dominance plasticity.
引用
收藏
页码:1569 / 1577
页数:9
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