Yu Wendou, De Blas Angel L
Department of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut 06269, USA.
J Neurochem. 2008 Feb;104(3):830-45. doi: 10.1111/j.1471-4159.2007.05014.x.
We have recently shown that disrupting the expression and post-synaptic clustering of gephyrin in cultured hippocampal pyramidal cells, by either gephyrin RNAi (RNA interference) or over-expression of a dominant negative gephyrin-enhanced green fluorescent protein (EGFP) fusion protein, leads to decreased number of post-synaptic gephyrin and GABA(A) receptor clusters and to reduced GABAergic innervation of these cells. On the other hand, increasing gephyrin expression led to a small increase in the number of gephyrin and GABA(A) receptor clusters and to little or no effect on GABAergic innervation. We are now reporting that altering gephyrin expression and clustering affects the size but not the density of glutamatergic synaptic contacts. Knocking down gephyrin with gephyrin RNAi, or preventing gephyrin clustering by over-expression of the dominant negative gephyrin-enhanced green fluorescent protein fusion protein, leads to larger post-synaptic PSD-95 clusters and larger pre-synaptic glutamatergic terminals. On the other hand, over-expression of gephyrin leads to slightly smaller PSD-95 clusters and pre-synaptic glutamatergic terminals. The change in size of PSD-95 clusters were accompanied by a parallel change in the size of NR2-NMDA receptor clusters. It is concluded that the levels of expression and clustering of gephyrin, a protein that concentrates at the post-synaptic complex of the inhibitory synapses, not only has homotypic effects on GABAergic synaptic contacts, but also has heterotypic effects on glutamatergic synaptic contacts. We are proposing that gephyrin is a counterpart of the post-synaptic glutamatergic scaffold protein PSD-95 in regulating the number and/or size of the excitatory and inhibitory synaptic contacts.
我们最近发现,通过gephyrin RNA干扰(RNAi)或显性负性gephyrin增强型绿色荧光蛋白(EGFP)融合蛋白的过表达,破坏培养的海马锥体神经元中gephyrin的表达和突触后聚集,会导致突触后gephyrin和GABA(A)受体簇数量减少,并减少这些细胞的GABA能神经支配。另一方面,增加gephyrin表达会导致gephyrin和GABA(A)受体簇数量略有增加,对GABA能神经支配几乎没有影响或没有影响。我们现在报告,改变gephyrin的表达和聚集会影响谷氨酸能突触接触的大小,但不影响其密度。用gephyrin RNAi敲低gephyrin,或通过显性负性gephyrin增强型绿色荧光蛋白融合蛋白的过表达来阻止gephyrin聚集,会导致突触后PSD-95簇和突触前谷氨酸能终末变大。另一方面,gephyrin的过表达会导致PSD-95簇和突触前谷氨酸能终末略小。PSD-95簇大小的变化伴随着NR2-NMDA受体簇大小的平行变化。得出的结论是,gephyrin是一种集中在抑制性突触突触后复合体的蛋白质,其表达和聚集水平不仅对GABA能突触接触有同型作用,而且对谷氨酸能突触接触有异型作用。我们提出,gephyrin在调节兴奋性和抑制性突触接触的数量和/或大小时,是突触后谷氨酸能支架蛋白PSD-95的对应物。