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Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement

Before the onset of hearing, cochlea-generated patterns of spontaneous spike activity drive the maturation of central auditory circuits. In the glycinergic sound localization pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO) this spontaneous activity gu...

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Autores principales: Bach, Eva C., Kandler, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547119/
https://www.ncbi.nlm.nih.gov/pubmed/33037263
http://dx.doi.org/10.1038/s41598-020-73050-y
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author Bach, Eva C.
Kandler, Karl
author_facet Bach, Eva C.
Kandler, Karl
author_sort Bach, Eva C.
collection PubMed
description Before the onset of hearing, cochlea-generated patterns of spontaneous spike activity drive the maturation of central auditory circuits. In the glycinergic sound localization pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO) this spontaneous activity guides the strengthening and silencing of synapses which underlies tonotopic map refinement. However, the mechanisms by which patterned activity regulates synaptic refinement in the MNTB-LSO pathway are still poorly understood. To address this question, we recorded from LSO neurons in slices from prehearing mice while stimulating MNTB afferents with stimulation patterns that mimicked those present in vivo. We found that these semi-natural stimulation patterns reliably elicited a novel form of long-term potentiation (LTP) of MNTB-LSO synapses. Stimulation patterns that lacked the characteristic high-frequency (200 Hz) component of prehearing spike activity failed to elicit potentiation. LTP was calcium dependent, required the activation of both g-protein coupled GABA(B) and metabotropic glutamate receptors and involved an increase in postsynaptic glycine receptor-mediated currents. Our results provide a possible mechanism linking spontaneous spike bursts to tonotopic map refinement and further highlight the importance of the co-release of GABA and glutamate from immature glycinergic MNTB terminals.
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spelling pubmed-75471192020-10-14 Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement Bach, Eva C. Kandler, Karl Sci Rep Article Before the onset of hearing, cochlea-generated patterns of spontaneous spike activity drive the maturation of central auditory circuits. In the glycinergic sound localization pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO) this spontaneous activity guides the strengthening and silencing of synapses which underlies tonotopic map refinement. However, the mechanisms by which patterned activity regulates synaptic refinement in the MNTB-LSO pathway are still poorly understood. To address this question, we recorded from LSO neurons in slices from prehearing mice while stimulating MNTB afferents with stimulation patterns that mimicked those present in vivo. We found that these semi-natural stimulation patterns reliably elicited a novel form of long-term potentiation (LTP) of MNTB-LSO synapses. Stimulation patterns that lacked the characteristic high-frequency (200 Hz) component of prehearing spike activity failed to elicit potentiation. LTP was calcium dependent, required the activation of both g-protein coupled GABA(B) and metabotropic glutamate receptors and involved an increase in postsynaptic glycine receptor-mediated currents. Our results provide a possible mechanism linking spontaneous spike bursts to tonotopic map refinement and further highlight the importance of the co-release of GABA and glutamate from immature glycinergic MNTB terminals. Nature Publishing Group UK 2020-10-09 /pmc/articles/PMC7547119/ /pubmed/33037263 http://dx.doi.org/10.1038/s41598-020-73050-y Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bach, Eva C.
Kandler, Karl
Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
title Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
title_full Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
title_fullStr Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
title_full_unstemmed Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
title_short Long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
title_sort long-term potentiation of glycinergic synapses by semi-natural stimulation patterns during tonotopic map refinement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547119/
https://www.ncbi.nlm.nih.gov/pubmed/33037263
http://dx.doi.org/10.1038/s41598-020-73050-y
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