Nicotinic regulation of experience-dependent plasticity in visual cortex

被引:14
作者
Sadahiro, Masato
Sajo, Mari
Morishita, Hirofumi
机构
[1] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Ophthalmol, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Mindich Child Hlth & Dev Inst, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
关键词
Visual cortex; Plasticity; Cholinergic; Nicotinic; Lynx1; Lypd6; TISSUE-PLASMINOGEN ACTIVATOR; FOREBRAIN CHOLINERGIC NEURONS; OCULAR DOMINANCE PLASTICITY; LONG-TERM POTENTIATION; ACETYLCHOLINE-RECEPTORS; POSTNATAL-DEVELOPMENT; DENDRITIC SPINES; CORTICAL PLASTICITY; PREFRONTAL CORTEX; RAT-BRAIN;
D O I
10.1016/j.jphysparis.2016.11.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
While the cholinergic neuromodulatory system and muscarinic acetylcholine receptors (AChRs) have been appreciated as permissive factors for developmental critical period plasticity in visual cortex, it was unknown why plasticity becomes limited after the critical period even in the presence of massive cholinergic projections to visual cortex. In this review we highlighted the recent progresses that started to shed light on the role of the nicotinic cholinergic neuromodulatory signaling on limiting juvenile form of plasticity in the adult brain. We introduce the Lynx family of proteins and Lynx1 as its representative, as endogenous proteins structurally similar to alpha-bungarotoxin with the ability to bind and modulate nAChRs to effectively regulate functional and structural plasticity, Remarkably, Lynx family members are expressed in distinct subpopulations of GABAergic interneurons, placing them in unique positions to potentially regulate the convergence of GABAergic and nicotinic neuromodulatory systems to regulate plasticity. Continuing studies of the potentially differential roles of Lynx family of proteins may further our understanding of the fundamentals of molecular and cell type-specific mechanisms of plasticity that we may be able to harness through nicotinic cholinergic signaling. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
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