Chen Xiaobing, Winters Christine, Azzam Rita, Li Xiang, Galbraith James A, Leapman Richard D, Reese Thomas S
Laboratory of Neurobiology and Electron Microscopy Facility, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4453-8. doi: 10.1073/pnas.0800897105. Epub 2008 Mar 7.
Much is known about the composition and function of the postsynaptic density (PSD), but less is known about its molecular organization. We use EM tomography to delineate the organization of PSDs at glutamatergic synapses in rat hippocampal cultures. The core of the PSD is dominated by vertically oriented filaments, and ImmunoGold labeling shows that PSD-95 is a component of these filaments. Vertical filaments contact two types of transmembrane structures whose sizes and positions match those of glutamate receptors and intermesh with two types of horizontally oriented filaments lying 10-20 nm from the postsynaptic membrane. The longer horizontal filaments link adjacent NMDAR-type structures, whereas the smaller filaments link both NMDA- and AMPAR-type structures. The orthogonal, interlinked scaffold of filaments at the core of the PSD provides a structural basis for understanding dynamic aspects of postsynaptic function.
我们对突触后致密物(PSD)的组成和功能了解颇多,但其分子组织却知之甚少。我们利用电子显微镜断层扫描技术描绘大鼠海马体培养物中谷氨酸能突触处PSD的组织情况。PSD的核心由垂直排列的细丝主导,免疫金标记显示PSD-95是这些细丝的一个组成部分。垂直细丝与两种跨膜结构接触,其大小和位置与谷氨酸受体相匹配,并与距离突触后膜10-20纳米的两种水平排列的细丝相互交织。较长的水平细丝连接相邻的NMDAR型结构,而较短的细丝则连接NMDA型和AMPAR型结构。PSD核心处细丝的正交、相互连接的支架为理解突触后功能的动态方面提供了结构基础。