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睁眼诱导PSD - 95在中枢视觉神经元中快速进行树突定位。

Eye opening induces a rapid dendritic localization of PSD-95 in central visual neurons.

作者信息

Yoshii Akira, Sheng Morgan H, Constantine-Paton Martha

机构信息

Department of Biology, Center for Learning and Memory, McGovern Institute for Brain Research, and Howard Hughes Medical Institute, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139-4307, USA.

出版信息

Proc Natl Acad Sci U S A. 2003 Feb 4;100(3):1334-9. doi: 10.1073/pnas.0335785100. Epub 2003 Jan 27.

Abstract

The membrane-associated guanylate kinase PSD-95 scaffolds N-methyl-d-aspartate receptors to cytoplasmic signaling molecules, and associates with other glutamate receptors at central synapses. However, regulation of PSD-95 in vivo is poorly understood. We provide evidence of an activity-dependent redistribution of PSD-95 to dendrites in central visual neurons that is tied to eye opening. Six hours after eye opening, increased dendritic PSD-95 coimmunoprecipitates with the same proportions of stargazin, increased proportions of the N-methyl-d-aspartate receptor subunit NR2A, and decreased proportions of NR2B. Sustained high levels of PSD-95 in dendrites are dependent on continued pattern vision in juvenile but not mature animals, suggesting that the stabilization of PSD-95 at synapses may be involved in the control of developmental plasticity.

摘要

与膜相关的鸟苷酸激酶PSD-95将N-甲基-D-天冬氨酸受体与细胞质信号分子搭建在一起,并在中枢突触处与其他谷氨酸受体相关联。然而,人们对PSD-95在体内的调节了解甚少。我们提供证据表明,在中枢视觉神经元中,PSD-95会因活动而重新分布到树突中,这与睁眼有关。睁眼6小时后,树突中PSD-95免疫共沉淀增加,其与相同比例的stargazin、增加比例的N-甲基-D-天冬氨酸受体亚基NR2A以及减少比例的NR2B共沉淀。树突中持续高水平的PSD-95依赖于幼年而非成年动物持续的模式视觉,这表明PSD-95在突触处的稳定可能参与了发育可塑性的控制。

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