Literature DB >> 7620614

Immunocytochemical localization of the alpha 1 and beta 2/3 subunits of the GABAA receptor in relation to specific GABAergic synapses in the dentate gyrus.

Z Nusser1, J D Roberts, A Baude, J G Richards, W Sieghart, P Somogyi.   

Abstract

Dentate granule cells receive spatially segregated GABAergic innervation from at least five types of local circuit neurons, and express mRNA for at least 11 subunits of the GABAA receptor. At most two to four different subunits are required to make a functional pentamer, raising the possibility that cells have on their surface several types of GABAA receptor channel, which may not be uniformly distributed. In order to establish the subcellular location of GABAA receptors on different parts of dentate neurons, the distribution of immunoreactivity for the alpha 1 and beta 2/3 subunits of the receptor was studied using high-resolution immunocytochemistry. Light microscopic immunoperoxidase reactions revealed strong GABAA receptor immunoreactivity in the molecular layer of the dentate gyrus. Pre-embedding immunogold localization of the alpha 1 and beta 2/3 subunits consistently showed extrasynaptic location of the GABAA receptor on the somatic, dendritic and axon initial segment membrane of granule cells, but failed to show receptors in synaptic junctions. Using a postembedding immunogold technique on freeze-substituted, Lowicryl-embedded tissue, synaptic enrichment of immunoreactivity for these subunits was found on both granule and non-principal cells. Only the postembedding immunogold method is suitable for revealing relative differences in receptor density at the subcellular level, giving approximately 20 nm resolution. The immunolabelling for GABAA receptor occupied the whole width of synaptic junctions, with a sharp decrease in labelling at the edge of the synaptic membrane specialization. Both subunits have been localized in the synaptic junctions between basket cell terminals and somata, and between axo-axonic cell terminals and axon initial segments of granule cells, with no qualitative difference in labelling. Receptor-immunopositive synapses were found at all depths of the molecular layer. Some of the boutons forming these dendritic synapses have been shown to contain GABA, providing evidence that some of the GABAergic cells that terminate only on the dendrites of granule cells also act through GABAA receptors. Double immunolabelling experiments demonstrated that a population of GABA-immunopositive neurons expresses a higher density of immunoreactive GABAA receptor on their surface than principal cells. Interneurons were found to receive GABAA receptor-positive synapses on their dendrites in the hilus, molecular and granule cell layers. Receptor-immunopositive synapses were also present throughout the hilus on presumed mossy cells. The results demonstrate that both granule cells and interneurons exhibit a compartmentalized distribution of the GABAA receptor on their surface, the postjunctional membrane to GABAergic terminals having the highest concentration of receptor.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7620614     DOI: 10.1111/j.1460-9568.1995.tb00667.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  40 in total

1.  Differential regulation of synaptic GABAA receptors by cAMP-dependent protein kinase in mouse cerebellar and olfactory bulb neurones.

Authors:  Z Nusser; W Sieghart; I Mody
Journal:  J Physiol       Date:  1999-12-01       Impact factor: 5.182

2.  Rapid signaling at inhibitory synapses in a dentate gyrus interneuron network.

Authors:  M Bartos; I Vida; M Frotscher; J R Geiger; P Jonas
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

3.  Composition of the GABA(A) receptors of retinal dopaminergic neurons.

Authors:  S Gustincich; A Feigenspan; W Sieghart; E Raviola
Journal:  J Neurosci       Date:  1999-09-15       Impact factor: 6.167

4.  Mismatched appositions of presynaptic and postsynaptic components in isolated hippocampal neurons.

Authors:  A Rao; E M Cha; A M Craig
Journal:  J Neurosci       Date:  2000-11-15       Impact factor: 6.167

5.  Subcellular and subsynaptic localization of presynaptic and postsynaptic kainate receptor subunits in the monkey striatum.

Authors:  J Z Kieval; G W Hubert; A Charara; J F Paré; Y Smith
Journal:  J Neurosci       Date:  2001-11-15       Impact factor: 6.167

Review 6.  Axon initial segment dysfunction in epilepsy.

Authors:  Verena C Wimmer; Christopher A Reid; Eva Y-W So; Samuel F Berkovic; Steven Petrou
Journal:  J Physiol       Date:  2010-04-07       Impact factor: 5.182

7.  Albumin induces excitatory synaptogenesis through astrocytic TGF-β/ALK5 signaling in a model of acquired epilepsy following blood-brain barrier dysfunction.

Authors:  Itai Weissberg; Lydia Wood; Lyn Kamintsky; Oscar Vazquez; Dan Z Milikovsky; Allyson Alexander; Hannah Oppenheim; Carolyn Ardizzone; Albert Becker; Federica Frigerio; Annamaria Vezzani; Marion S Buckwalter; John R Huguenard; Alon Friedman; Daniela Kaufer
Journal:  Neurobiol Dis       Date:  2015-03-30       Impact factor: 5.996

8.  Increased efficiency of the GABAA and GABAB receptor-mediated neurotransmission in the Ts65Dn mouse model of Down syndrome.

Authors:  Alexander M Kleschevnikov; Pavel V Belichenko; Jessica Gall; Lizzy George; Rachel Nosheny; Michael T Maloney; Ahmad Salehi; William C Mobley
Journal:  Neurobiol Dis       Date:  2011-10-17       Impact factor: 5.996

Review 9.  Defined types of cortical interneurone structure space and spike timing in the hippocampus.

Authors:  Peter Somogyi; Thomas Klausberger
Journal:  J Physiol       Date:  2004-11-11       Impact factor: 5.182

10.  Analysis of the excitatory and inhibitory components of postsynaptic currents recorded in pyramidal neurons and interneurons in the rat hippocampus.

Authors:  S L Buldakova; D B Tikhonov; L G Magazanik
Journal:  Neurosci Behav Physiol       Date:  2005-10
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