Yoshii Akira, Sheng Morgan H, Constantine-Paton Martha
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.
Proc Natl Acad Sci U S A. 2003 Feb 4;100(3):1334-9. doi: 10.1073/pnas.0335785100. Epub 2003 Jan 27.
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.
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。