Studler B, Fritschy J-M, Brünig I
Institute of Pharmacology and Toxicology, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Neuroscience. 2002;114(1):123-33. doi: 10.1016/s0306-4522(02)00206-3.
Synapse formation in CNS neurons requires appropriate sorting and clustering of neurotransmitter receptors and associated proteins at postsynaptic sites. In GABAergic synapses, clustering of GABA(A) receptors requires gephyrin, but it is not known whether presynaptic signals are also involved in this process. To investigate this issue, we analyzed the subcellular distribution of GABA(A) receptors and gephyrin in primary cultures of cerebellar granule cells, by comparing cells receiving GABAergic input with cells devoid of such afferents. Using immunofluorescence staining, we show that the GABA(A) receptor alpha1 and gamma2 subunit, but not alpha6 or delta subunit, form clusters co-localized with gephyrin in granule cell neurites, irrespective of the presence of GABAergic axons. GABAergic terminals typically were surrounded by groups of gephyrin clusters, pointing to the presence of multiple synaptic sites. In contrast, in neurites devoid of GABAergic input, gephyrin clusters were distributed at random and apposed to glutamatergic terminals, suggesting the formation of mismatched synapses. Both populations of gephyrin clusters were co-localized with GABA(A) receptor subunits, indicating that these proteins are associated also in non-GABAergic synapses. To determine whether signaling mediated by GABA(A) receptors is required for the formation of appropriately matched gephyrin clusters, cultures were treated chronically with bicuculline, or with either muscimol or 4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol. All these treatments failed to influence the distribution of gephyrin clusters. We conclude that although GABAergic presynaptic terminals have a preponderant influence on the distribution of gephyrin clusters in dendrites of cerebellar granule cells, GABA transmission is dispensable for postsynaptic clustering of gephyrin and GABA(A) receptors and for the formation of appropriately matched GABAergic synapses.
中枢神经系统(CNS)神经元中的突触形成需要神经递质受体和相关蛋白在突触后位点进行适当的分选和聚集。在GABA能突触中,GABA(A)受体的聚集需要gephyrin,但尚不清楚突触前信号是否也参与这一过程。为了研究这个问题,我们通过比较接受GABA能输入的细胞和没有这种传入神经的细胞,分析了小脑颗粒细胞原代培养物中GABA(A)受体和gephyrin的亚细胞分布。利用免疫荧光染色,我们发现GABA(A)受体α1和γ2亚基,而不是α6或δ亚基,在颗粒细胞神经突中形成与gephyrin共定位的簇,无论是否存在GABA能轴突。GABA能终末通常被gephyrin簇群包围,表明存在多个突触位点。相比之下,在没有GABA能输入的神经突中,gephyrin簇随机分布并与谷氨酸能终末相邻,提示形成了错配突触。这两种gephyrin簇群均与GABA(A)受体亚基共定位,表明这些蛋白在非GABA能突触中也有关联。为了确定GABA(A)受体介导的信号传导是否是形成适当匹配的gephyrin簇所必需的,培养物用荷包牡丹碱、蝇蕈醇或4,5,6,7-四氢异恶唑并[5,4-c]吡啶-3-醇进行长期处理。所有这些处理均未能影响gephyrin簇的分布。我们得出结论,尽管GABA能突触前终末对小脑颗粒细胞树突中gephyrin簇的分布有主要影响,但GABA传递对于gephyrin和GABA(A)受体的突触后聚集以及形成适当匹配的GABA能突触是可有可无的。