Christie Sean B, Miralles Celia P, De Blas Angel L
Department of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut 06269, USA.
J Neurosci. 2002 Feb 1;22(3):684-97. doi: 10.1523/JNEUROSCI.22-03-00684.2002.
We have studied the effects of GABAergic innervation on the clustering of GABA(A) receptors (GABA(A)Rs) in cultured hippocampal neurons. In the absence of GABAergic innervation, pyramidal cells form small (0.36 +/- 0.01 micrometer diameter) GABA(A)R clusters at their surface in the dendrites and soma. When receiving GABAergic innervation from glutamic acid decarboxylase-containing interneurons, pyramidal cells form large (1.62 +/- 0.08 micrometer breadth) GABA(A)R clusters at GABAergic synapses. This is accompanied by a disappearance of the small GABA(A)R clusters in the local area surrounding each GABAergic synapse. Although the large synaptic GABA(A)R clusters of any neuron contained all GABA(A)R subunits and isoforms expressed by that neuron, the small clusters not localized at GABAergic synapses showed significant heterogeneity in subunit and isoform composition. Another difference between large GABAergic and small non-GABAergic GABA(A)R clusters was that a significant proportion of the latter was juxtaposed to postsynaptic markers of glutamatergic synapses such as PSD-95 and AMPA receptor GluR1 subunit. The densities of both the glutamate receptor-associated and non-associated small GABA(A)R clusters were decreased in areas surrounding GABAergic synapses. However, no effect on the density or distribution of glutamate receptor clusters was observed. The results suggest that there are local signals generated at GABAergic synapses that induce both assembly of large synaptic GABA(A)R clusters at the synapse and disappearance of the small GABA(A)R clusters in the surrounding area. In the absence of GABAergic innervation, weaker GABA(A)R-clustering signals, generated at glutamatergic synapses, induce the formation of small postsynaptic GABA(A)R clusters that remain juxtaposed to glutamate receptors at glutamatergic synapses.
我们研究了GABA能神经支配对培养的海马神经元中GABA(A)受体(GABA(A)Rs)聚集的影响。在没有GABA能神经支配的情况下,锥体细胞在其树突和胞体表面形成小的(直径0.36±0.01微米)GABA(A)R簇。当从含谷氨酸脱羧酶的中间神经元接受GABA能神经支配时,锥体细胞在GABA能突触处形成大的(宽度1.62±0.08微米)GABA(A)R簇。这伴随着每个GABA能突触周围局部区域中小GABA(A)R簇的消失。尽管任何神经元的大的突触GABA(A)R簇包含该神经元表达的所有GABA(A)R亚基和亚型,但未定位在GABA能突触处的小簇在亚基和亚型组成上表现出显著的异质性。大的GABA能和小的非GABA能GABA(A)R簇之间的另一个差异是,后者的很大一部分与谷氨酸能突触的突触后标记物如PSD - 95和AMPA受体GluR1亚基并列。谷氨酸受体相关和不相关的小GABA(A)R簇的密度在GABA能突触周围区域均降低。然而,未观察到对谷氨酸受体簇的密度或分布有影响。结果表明,在GABA能突触处产生局部信号,这些信号既诱导突触处大的突触GABA(A)R簇的组装,又诱导周围区域中小GABA(A)R簇的消失。在没有GABA能神经支配的情况下,在谷氨酸能突触处产生的较弱的GABA(A)R聚集信号诱导形成小的突触后GABA(A)R簇,这些小簇在谷氨酸能突触处与谷氨酸受体并列。