4.5 Article

Selective localization of collybistin at a subset of inhibitory synapses in brain circuits

期刊

JOURNAL OF COMPARATIVE NEUROLOGY
卷 520, 期 1, 页码 130-141

出版社

WILEY
DOI: 10.1002/cne.22702

关键词

gephyrin; GABAA receptor; receptor clustering; GABAergic synapses

资金

  1. Compagnia di San Paolo, Regione Piemonte [Ricerca Sanitaria Finalizzata 2008, 2008/bis]
  2. Medical Research Council [G0501258]
  3. MRC [G0800498, G0501258] Funding Source: UKRI
  4. Medical Research Council [G0501258, G0800498] Funding Source: researchfish

向作者/读者索取更多资源

Collybistin is a brain-specific guanine nucleotide exchange factor (GEF) that is crucial for the postsynaptic accumulation of gephyrin and ?-aminobutyric acid A receptors (GABAARs) at a specific subset of inhibitory synapses. Our understanding of the in vivo function of collybistin has been hampered by lack of information about the synaptic localization of this protein in brain circuits. Here we describe the subcellular localization of endogenous collybistin by using antibodies raised against distinct molecular domains that should recognize the majority of endogenous collybistin isoforms. We show that collybistin co-clusters with gephyrin and GABAARs in synaptic puncta and is recruited to postsynaptic specializations early during synapse development. Notably, collybistin is present in only a subset of gephyrin-positive synapses, with variable co-localization values in different brain regions. Moreover, collybistin co-localizes with GABAARs containing the a1, a2, or a3 subunits, arguing against a selective association with specific GABAAR subtypes. Surprisingly, we found that collybistin is expressed only transiently in Purkinje cells, suggesting that in these cerebellar neurons collybistin plays a selective role during the initial assembly of postsynaptic specializations. These data reveal a remarkable heterogeneity in the organization of GABAergic synapses and provide an anatomical basis for interpreting the variable effects caused by disruption of the collybistin gene in human X-linked intellectual disability and mouse knockout models. J. Comp. Neurol., 2012. (c) 2011 Wiley Periodicals, Inc.

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