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The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice
BACKGROUND: The vesicular GABA transporter (VGAT) loads GABA and glycine from the neuronal cytoplasm into synaptic vesicles. To address functional importance of VGAT during embryonic development, we generated global VGAT knockout mice and analyzed them. RESULTS: VGAT knockouts at embryonic day (E) 1...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023674/ https://www.ncbi.nlm.nih.gov/pubmed/21190592 http://dx.doi.org/10.1186/1756-6606-3-40 |
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author | Saito, Kenzi Kakizaki, Toshikazu Hayashi, Ryotaro Nishimaru, Hiroshi Furukawa, Tomonori Nakazato, Yoichi Takamori, Shigeo Ebihara, Satoe Uematsu, Masakazu Mishina, Masayoshi Miyazaki, Jun-ichi Yokoyama, Minesuke Konishi, Shiro Inoue, Koichi Fukuda, Atsuo Fukumoto, Manabu Nakamura, Kenji Obata, Kunihiko Yanagawa, Yuchio |
author_facet | Saito, Kenzi Kakizaki, Toshikazu Hayashi, Ryotaro Nishimaru, Hiroshi Furukawa, Tomonori Nakazato, Yoichi Takamori, Shigeo Ebihara, Satoe Uematsu, Masakazu Mishina, Masayoshi Miyazaki, Jun-ichi Yokoyama, Minesuke Konishi, Shiro Inoue, Koichi Fukuda, Atsuo Fukumoto, Manabu Nakamura, Kenji Obata, Kunihiko Yanagawa, Yuchio |
author_sort | Saito, Kenzi |
collection | PubMed |
description | BACKGROUND: The vesicular GABA transporter (VGAT) loads GABA and glycine from the neuronal cytoplasm into synaptic vesicles. To address functional importance of VGAT during embryonic development, we generated global VGAT knockout mice and analyzed them. RESULTS: VGAT knockouts at embryonic day (E) 18.5 exhibited substantial increases in overall GABA and glycine, but not glutamate, contents in the forebrain. Electrophysiological recordings from E17.5-18.5 spinal cord motoneurons demonstrated that VGAT knockouts presented no spontaneous inhibitory postsynaptic currents mediated by GABA and glycine. Histological examination of E18.5 knockout fetuses revealed reductions in the trapezius muscle, hepatic congestion and little alveolar spaces in the lung, indicating that the development of skeletal muscle, liver and lung in these mice was severely affected. CONCLUSION: VGAT is fundamental for the GABA- and/or glycine-mediated transmission that supports embryonic development. VGAT knockout mice will be useful for further investigating the roles of VGAT in normal physiology and pathophysiologic processes. |
format | Text |
id | pubmed-3023674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30236742011-01-20 The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice Saito, Kenzi Kakizaki, Toshikazu Hayashi, Ryotaro Nishimaru, Hiroshi Furukawa, Tomonori Nakazato, Yoichi Takamori, Shigeo Ebihara, Satoe Uematsu, Masakazu Mishina, Masayoshi Miyazaki, Jun-ichi Yokoyama, Minesuke Konishi, Shiro Inoue, Koichi Fukuda, Atsuo Fukumoto, Manabu Nakamura, Kenji Obata, Kunihiko Yanagawa, Yuchio Mol Brain Research BACKGROUND: The vesicular GABA transporter (VGAT) loads GABA and glycine from the neuronal cytoplasm into synaptic vesicles. To address functional importance of VGAT during embryonic development, we generated global VGAT knockout mice and analyzed them. RESULTS: VGAT knockouts at embryonic day (E) 18.5 exhibited substantial increases in overall GABA and glycine, but not glutamate, contents in the forebrain. Electrophysiological recordings from E17.5-18.5 spinal cord motoneurons demonstrated that VGAT knockouts presented no spontaneous inhibitory postsynaptic currents mediated by GABA and glycine. Histological examination of E18.5 knockout fetuses revealed reductions in the trapezius muscle, hepatic congestion and little alveolar spaces in the lung, indicating that the development of skeletal muscle, liver and lung in these mice was severely affected. CONCLUSION: VGAT is fundamental for the GABA- and/or glycine-mediated transmission that supports embryonic development. VGAT knockout mice will be useful for further investigating the roles of VGAT in normal physiology and pathophysiologic processes. BioMed Central 2010-12-30 /pmc/articles/PMC3023674/ /pubmed/21190592 http://dx.doi.org/10.1186/1756-6606-3-40 Text en Copyright ©2010 Saito et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Saito, Kenzi Kakizaki, Toshikazu Hayashi, Ryotaro Nishimaru, Hiroshi Furukawa, Tomonori Nakazato, Yoichi Takamori, Shigeo Ebihara, Satoe Uematsu, Masakazu Mishina, Masayoshi Miyazaki, Jun-ichi Yokoyama, Minesuke Konishi, Shiro Inoue, Koichi Fukuda, Atsuo Fukumoto, Manabu Nakamura, Kenji Obata, Kunihiko Yanagawa, Yuchio The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice |
title | The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice |
title_full | The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice |
title_fullStr | The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice |
title_full_unstemmed | The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice |
title_short | The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout mice |
title_sort | physiological roles of vesicular gaba transporter during embryonic development: a study using knockout mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023674/ https://www.ncbi.nlm.nih.gov/pubmed/21190592 http://dx.doi.org/10.1186/1756-6606-3-40 |
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