Affiliated with Université Laval & CERVO Research Centre

Gephyrin clusters are absent from small diameter primary afferent terminals despite the presence of GABA(A) receptors.

TitleGephyrin clusters are absent from small diameter primary afferent terminals despite the presence of GABA(A) receptors.
Publication TypeJournal Article
Year of Publication2014
AuthorsLorenzo L-E, Godin AG, Wang F, St-Louis M, Carbonetto S, Wiseman PW, Ribeiro-da-Silva A, De Koninck Y
JournalJ Neurosci
Volume34
Issue24
Pagination8300-17
Date Published2014 Jun 11
ISSN1529-2401
KeywordsAnimals, Calcitonin Gene-Related Peptide, Carrier Proteins, Lectins, Male, Membrane Proteins, Neurons, Afferent, Presynaptic Terminals, Rats, Rats, Sprague-Dawley, Receptors, GABA-A, Receptors, Glycine, Spinal Cord
Abstract

Whereas both GABA(A) receptors (GABA(A)Rs) and glycine receptors (GlyRs) play a role in control of dorsal horn neuron excitability, their relative contribution to inhibition of small diameter primary afferent terminals remains controversial. To address this, we designed an approach for quantitative analyses of the distribution of GABA(A)R-subunits, GlyR α1-subunit and their anchoring protein, gephyrin, on terminals of rat spinal sensory afferents identified by Calcitonin-Gene-Related-Peptide (CGRP) for peptidergic terminals, and by Isolectin-B4 (IB4) for nonpeptidergic terminals. The approach was designed for light microscopy, which is compatible with the mild fixation conditions necessary for immunodetection of several of these antigens. An algorithm was designed to recognize structures with dimensions similar to those of the microscope resolution. To avoid detecting false colocalization, the latter was considered significant only if the degree of pixel overlap exceeded that expected from randomly overlapping pixels given a hypergeometric distribution. We found that both CGRP(+) and IB4(+) terminals were devoid of GlyR α1-subunit and gephyrin. The α1 GABA(A)R was also absent from these terminals. In contrast, the GABA(A)R α2/α3/α5 and β3 subunits were significantly expressed in both terminal types, as were other GABA(A)R-associated-proteins (α-Dystroglycan/Neuroligin-2/Collybistin-2). Ultrastructural immunocytochemistry confirmed the presence of GABA(A)R β3 subunits in small afferent terminals. Real-time quantitative PCR (qRT-PCR) confirmed the results of light microscopy immunochemical analysis. These results indicate that dorsal horn inhibitory synapses follow different rules of organization at presynaptic versus postsynaptic sites (nociceptive afferent terminals vs inhibitory synapses on dorsal horn neurons). The absence of gephyrin clusters from primary afferent terminals suggests a more diffuse mode of GABA(A)-mediated transmission at presynaptic than at postsynaptic sites.

DOI10.1523/JNEUROSCI.0159-14.2014
Alternate JournalJ. Neurosci.
PubMed ID24920633
Grant ListMOP-12942 / / Canadian Institutes of Health Research / Canada
MOP-79411 / / Canadian Institutes of Health Research / Canada