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Lynx1,一种胆碱能制动器,限制了成年视觉皮层的可塑性。

Lynx1, a cholinergic brake, limits plasticity in adult visual cortex.

机构信息

FM Kirby Neurobiology Center, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Science. 2010 Nov 26;330(6008):1238-40. doi: 10.1126/science.1195320. Epub 2010 Nov 11.

Abstract

Experience-dependent brain plasticity typically declines after an early critical period during which circuits are established. Loss of plasticity with closure of the critical period limits improvement of function in adulthood, but the mechanisms that change the brain's plasticity remain poorly understood. Here, we identified an increase in expression of Lynx1 protein in mice that prevented plasticity in the primary visual cortex late in life. Removal of this molecular brake enhanced nicotinic acetylcholine receptor signaling. Lynx1 expression thus maintains stability of mature cortical networks in the presence of cholinergic innervation. The results suggest that modulating the balance between excitatory and inhibitory circuits reactivates visual plasticity and may present a therapeutic target.

摘要

经验依赖型大脑可塑性通常在早期关键期过后下降,在此期间,回路得以建立。关键期结束后可塑性的丧失限制了成年后功能的改善,但改变大脑可塑性的机制仍知之甚少。在这里,我们发现 Lynx1 蛋白在小鼠中的表达增加,从而阻止了生命后期初级视觉皮层的可塑性。去除这种分子刹车增强了烟碱型乙酰胆碱受体信号。因此,Lynx1 表达在胆碱能神经支配存在的情况下维持成熟皮质网络的稳定性。研究结果表明,调节兴奋性和抑制性回路之间的平衡可以重新激活视觉可塑性,这可能是一个治疗靶点。

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