Literature DB >> 12207960

GABAergic and glutamatergic terminals differentially influence the organization of GABAergic synapses in rat cerebellar granule cells in vitro.

B Studler1, J-M Fritschy, I Brünig.   

Abstract

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. Copyright 2002 IBRO

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Year:  2002        PMID: 12207960     DOI: 10.1016/s0306-4522(02)00206-3

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  7 in total

1.  Transmitter-receptor mismatch in GABAergic synapses in the absence of activity.

Authors:  Roberta Cesa; Laura Morando; Piergiorgio Strata
Journal:  Proc Natl Acad Sci U S A       Date:  2008-11-19       Impact factor: 11.205

Review 2.  Emerging themes in GABAergic synapse development.

Authors:  Marissa S Kuzirian; Suzanne Paradis
Journal:  Prog Neurobiol       Date:  2011-07-20       Impact factor: 11.685

3.  Knockout of the γ-aminobutyric acid receptor subunit α4 reduces functional δ-containing extrasynaptic receptors in hippocampal pyramidal cells at the onset of puberty.

Authors:  Nicole Sabaliauskas; Hui Shen; Gregg E Homanics; Sheryl S Smith; Chiye Aoki
Journal:  Brain Res       Date:  2012-02-22       Impact factor: 3.252

4.  Deletion of the NR2A subunit prevents developmental changes of NMDA-mEPSCs in cultured mouse cerebellar granule neurones.

Authors:  Zhanyan Fu; Stephen M Logan; Stefano Vicini
Journal:  J Physiol       Date:  2005-01-13       Impact factor: 5.182

5.  Gephyrin alterations due to protein accumulation stress are reduced by the lysosomal modulator Z-Phe-Ala-diazomethylketone.

Authors:  Sophia Ryzhikov; Ben A Bahr
Journal:  J Mol Neurosci       Date:  2007-09-18       Impact factor: 3.444

6.  GluRdelta2 expression in the mature cerebellum of hotfoot mice promotes parallel fiber synaptogenesis and axonal competition.

Authors:  Georgia Mandolesi; Eleonora Autuori; Roberta Cesa; Federica Premoselli; Paolo Cesare; Piergiorgio Strata
Journal:  PLoS One       Date:  2009-04-16       Impact factor: 3.240

7.  Presynaptic terminals independently regulate synaptic clustering and autophagy of GABAA receptors in Caenorhabditis elegans.

Authors:  Aaron M Rowland; Janet E Richmond; Jason G Olsen; David H Hall; Bruce A Bamber
Journal:  J Neurosci       Date:  2006-02-08       Impact factor: 6.167

  7 in total

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