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...

Descripción completa

Detalles Bibliográficos
Autores principales: Theisen, Ulrike, Hey, Sven, Hennig, Christian D., Schnabel, Ralf, Köster, Reinhard W.
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