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Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal

The physiological functions of glycine receptors (GlyRs) depend on their subcellular locations. In axonal terminals of the central neurons, GlyRs trigger a slow facilitation of presynaptic transmitter release; however, their spatial relationship to the release sites is not known. In this study, we e...

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Autores principales: Trojanova, Johana, Kulik, Akos, Janacek, Jiri, Kralikova, Michaela, Syka, Josef, Turecek, Rostislav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186306/
https://www.ncbi.nlm.nih.gov/pubmed/25339867
http://dx.doi.org/10.3389/fncir.2014.00120
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author Trojanova, Johana
Kulik, Akos
Janacek, Jiri
Kralikova, Michaela
Syka, Josef
Turecek, Rostislav
author_facet Trojanova, Johana
Kulik, Akos
Janacek, Jiri
Kralikova, Michaela
Syka, Josef
Turecek, Rostislav
author_sort Trojanova, Johana
collection PubMed
description The physiological functions of glycine receptors (GlyRs) depend on their subcellular locations. In axonal terminals of the central neurons, GlyRs trigger a slow facilitation of presynaptic transmitter release; however, their spatial relationship to the release sites is not known. In this study, we examined the distribution of GlyRs in the rat glutamatergic calyx of Held nerve terminal using high-resolution pre-embedding immunoelectron microscopy. We performed a quantitative analysis of GlyR-associated immunogold (IG) labeling in 3D reconstructed calyceal segments. A variable density of IG particles and their putative accumulations, inferred from the frequency distribution of inter-IG distances, indicated a non-uniform distribution of the receptors in the calyx. Subsequently, increased densities of IG particles were found in calyceal swellings, structures characterized by extensive exocytosis of glutamate. In swellings as well as in larger calyceal stalks, IG particles did not tend to accumulate near the glutamate releasing zones. On the other hand, GlyRs in swellings (but not in stalks) preferentially occupied membrane regions, unconnected to postsynaptic cells and presumably accessible by ambient glycine. Furthermore, the sites with increased GlyR concentrations were found in swellings tightly juxtaposed with GABA/glycinergic nerve endings. Thus, the results support the concept of an indirect mechanism underlying the modulatory effects of calyceal GlyRs, activated by glycine spillover. We also suggest the existence of an activity-dependent mechanism regulating the surface distribution of α homomeric GlyRs in axonal terminals of central neurons.
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spelling pubmed-41863062014-10-22 Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal Trojanova, Johana Kulik, Akos Janacek, Jiri Kralikova, Michaela Syka, Josef Turecek, Rostislav Front Neural Circuits Neuroscience The physiological functions of glycine receptors (GlyRs) depend on their subcellular locations. In axonal terminals of the central neurons, GlyRs trigger a slow facilitation of presynaptic transmitter release; however, their spatial relationship to the release sites is not known. In this study, we examined the distribution of GlyRs in the rat glutamatergic calyx of Held nerve terminal using high-resolution pre-embedding immunoelectron microscopy. We performed a quantitative analysis of GlyR-associated immunogold (IG) labeling in 3D reconstructed calyceal segments. A variable density of IG particles and their putative accumulations, inferred from the frequency distribution of inter-IG distances, indicated a non-uniform distribution of the receptors in the calyx. Subsequently, increased densities of IG particles were found in calyceal swellings, structures characterized by extensive exocytosis of glutamate. In swellings as well as in larger calyceal stalks, IG particles did not tend to accumulate near the glutamate releasing zones. On the other hand, GlyRs in swellings (but not in stalks) preferentially occupied membrane regions, unconnected to postsynaptic cells and presumably accessible by ambient glycine. Furthermore, the sites with increased GlyR concentrations were found in swellings tightly juxtaposed with GABA/glycinergic nerve endings. Thus, the results support the concept of an indirect mechanism underlying the modulatory effects of calyceal GlyRs, activated by glycine spillover. We also suggest the existence of an activity-dependent mechanism regulating the surface distribution of α homomeric GlyRs in axonal terminals of central neurons. Frontiers Media S.A. 2014-10-06 /pmc/articles/PMC4186306/ /pubmed/25339867 http://dx.doi.org/10.3389/fncir.2014.00120 Text en Copyright © 2014 Trojanova, Kulik, Janacek, Kralikova, Syka and Turecek. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Trojanova, Johana
Kulik, Akos
Janacek, Jiri
Kralikova, Michaela
Syka, Josef
Turecek, Rostislav
Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal
title Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal
title_full Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal
title_fullStr Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal
title_full_unstemmed Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal
title_short Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal
title_sort distribution of glycine receptors on the surface of the mature calyx of held nerve terminal
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186306/
https://www.ncbi.nlm.nih.gov/pubmed/25339867
http://dx.doi.org/10.3389/fncir.2014.00120
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