Cargando…
Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration
Various neurotransmitters influence neuronal migration in the developing zebrafish hindbrain. Migrating tegmental hindbrain nuclei neurons (THNs) are governed by depolarizing neurotransmitters (acetylcholine and glutamate), and glycine. In mature neurons, glycine binds to its receptor to hyperpolari...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132429/ https://www.ncbi.nlm.nih.gov/pubmed/30214676 http://dx.doi.org/10.1080/19420889.2018.1493324 |
_version_ | 1783354320025026560 |
---|---|
author | Theisen, Ulrike Hey, Sven Hennig, Christian D. Schnabel, Ralf Köster, Reinhard W. |
author_facet | Theisen, Ulrike Hey, Sven Hennig, Christian D. Schnabel, Ralf Köster, Reinhard W. |
author_sort | Theisen, Ulrike |
collection | PubMed |
description | Various neurotransmitters influence neuronal migration in the developing zebrafish hindbrain. Migrating tegmental hindbrain nuclei neurons (THNs) are governed by depolarizing neurotransmitters (acetylcholine and glutamate), and glycine. In mature neurons, glycine binds to its receptor to hyperpolarize cells. This effect depends on the co-expression of the solute carrier KCC2. Immature precursors, however, typically express NKCC1 instead of KCC2, leading to membrane depolarization upon glycine receptor activation. As neuronal migration occurs in neurons after leaving the cell cycle and before terminal differentiation, we hypothesized that the switch from NKCC1 to KCC2 expression could alter the effect of glycine on THN migration. We tested this notion using in vivo cell tracking, overexpression of glycine receptor mutations and whole mount in situ hybridization. We summarize our findings in a speculative model, combining developmental age, glycine receptor strength and solute carrier expression to describe the effect of glycine on the migration of THNs. |
format | Online Article Text |
id | pubmed-6132429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-61324292018-09-13 Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration Theisen, Ulrike Hey, Sven Hennig, Christian D. Schnabel, Ralf Köster, Reinhard W. Commun Integr Biol Short Communication Various neurotransmitters influence neuronal migration in the developing zebrafish hindbrain. Migrating tegmental hindbrain nuclei neurons (THNs) are governed by depolarizing neurotransmitters (acetylcholine and glutamate), and glycine. In mature neurons, glycine binds to its receptor to hyperpolarize cells. This effect depends on the co-expression of the solute carrier KCC2. Immature precursors, however, typically express NKCC1 instead of KCC2, leading to membrane depolarization upon glycine receptor activation. As neuronal migration occurs in neurons after leaving the cell cycle and before terminal differentiation, we hypothesized that the switch from NKCC1 to KCC2 expression could alter the effect of glycine on THN migration. We tested this notion using in vivo cell tracking, overexpression of glycine receptor mutations and whole mount in situ hybridization. We summarize our findings in a speculative model, combining developmental age, glycine receptor strength and solute carrier expression to describe the effect of glycine on the migration of THNs. Taylor & Francis 2018-08-13 /pmc/articles/PMC6132429/ /pubmed/30214676 http://dx.doi.org/10.1080/19420889.2018.1493324 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Theisen, Ulrike Hey, Sven Hennig, Christian D. Schnabel, Ralf Köster, Reinhard W. Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
title | Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
title_full | Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
title_fullStr | Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
title_full_unstemmed | Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
title_short | Glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
title_sort | glycine is able to induce both a motility speed in- and decrease during zebrafish neuronal migration |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132429/ https://www.ncbi.nlm.nih.gov/pubmed/30214676 http://dx.doi.org/10.1080/19420889.2018.1493324 |
work_keys_str_mv | AT theisenulrike glycineisabletoinducebothamotilityspeedinanddecreaseduringzebrafishneuronalmigration AT heysven glycineisabletoinducebothamotilityspeedinanddecreaseduringzebrafishneuronalmigration AT hennigchristiand glycineisabletoinducebothamotilityspeedinanddecreaseduringzebrafishneuronalmigration AT schnabelralf glycineisabletoinducebothamotilityspeedinanddecreaseduringzebrafishneuronalmigration AT kosterreinhardw glycineisabletoinducebothamotilityspeedinanddecreaseduringzebrafishneuronalmigration |