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突触前NMDA受体——体外和体内发育轴突中的动力学与分布

Presynaptic NMDA receptors - dynamics and distribution in developing axons in vitro and in vivo.

作者信息

Gill Ishwar, Droubi Sammy, Giovedi Silvia, Fedder Karlie N, Bury Luke A D, Bosco Federica, Sceniak Michael P, Benfenati Fabio, Sabo Shasta L

机构信息

Department of Pharmacology, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.

Department of Experimental Medicine, University of Genoa, 16132 Genoa, Italy.

出版信息

J Cell Sci. 2015 Feb 15;128(4):768-80. doi: 10.1242/jcs.162362. Epub 2014 Dec 19.

Abstract

During cortical development, N-methyl-D-aspartate (NMDA) receptors (NMDARs) facilitate presynaptic terminal formation, enhance neurotransmitter release and are required in presynaptic neurons for spike-timing-dependent long-term depression (tLTD). However, the extent to which NMDARs are found within cortical presynaptic terminals has remained controversial, and the sub-synaptic localization and dynamics of axonal NMDARs are unknown. Here, using live confocal imaging and biochemical purification of presynaptic membranes, we provide strong evidence that NMDARs localize to presynaptic terminals in vitro and in vivo in a developmentally regulated manner. The NR1 and NR2B subunits (also known as GRIN1 and GRIN2B, respectively) were found within the active zone membrane, where they could respond to synaptic glutamate release. Surprisingly, NR1 also appeared in glutamatergic and GABAergic synaptic vesicles. During synaptogenesis, NR1 was mobile throughout axons - including growth cones and filopodia, structures that are involved in synaptogenesis. Upon synaptogenic contact, NMDA receptors were quickly recruited to terminals by neuroligin-1 signaling. Unlike dendrites, the trafficking and distribution of axonal NR1 were insensitive to activity changes, including NMDA exposure, local glutamate uncaging or action potential blockade. These results support the idea that presynaptic NMDARs play an early role in presynaptic development.

摘要

在皮质发育过程中,N-甲基-D-天冬氨酸(NMDA)受体(NMDARs)促进突触前终末形成,增强神经递质释放,并且在突触前神经元中是依赖于峰电位时间的长时程抑制(tLTD)所必需的。然而,在皮质突触前终末中发现NMDARs的程度一直存在争议,并且轴突NMDARs的突触亚定位和动力学尚不清楚。在这里,我们使用实时共聚焦成像和突触前膜的生化纯化,提供了强有力的证据表明,NMDARs在体外和体内以发育调控的方式定位于突触前终末。在活性区膜内发现了NR1和NR2B亚基(分别也称为GRIN1和GRIN2B),它们能够对突触谷氨酸释放作出反应。令人惊讶的是,NR1也出现在谷氨酸能和γ-氨基丁酸能突触小泡中。在突触发生过程中,NR1在整个轴突中是可移动的——包括生长锥和丝状伪足,这些结构参与突触发生。在突触发生接触时,NMDA受体通过neuroligin-1信号迅速被招募到终末。与树突不同,轴突NR1的运输和分布对活性变化不敏感,包括NMDA暴露、局部谷氨酸解笼或动作电位阻断。这些结果支持了突触前NMDARs在突触前发育中起早期作用的观点。

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