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Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X
Lamina X of the spinal cord is a functionally diverse area with roles in locomotion, autonomic control and processing of mechano and nociceptive information. It is also a neurochemically diverse region. However, the different populations of cells in lamina X remain to be fully characterised. To dete...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier/North-Holland Biomedical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986852/ https://www.ncbi.nlm.nih.gov/pubmed/27378584 http://dx.doi.org/10.1016/j.brainres.2016.07.001 |
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author | Gotts, Jittima Atkinson, Lucy Yanagawa, Yuchio Deuchars, Jim Deuchars, Susan A. |
author_facet | Gotts, Jittima Atkinson, Lucy Yanagawa, Yuchio Deuchars, Jim Deuchars, Susan A. |
author_sort | Gotts, Jittima |
collection | PubMed |
description | Lamina X of the spinal cord is a functionally diverse area with roles in locomotion, autonomic control and processing of mechano and nociceptive information. It is also a neurochemically diverse region. However, the different populations of cells in lamina X remain to be fully characterised. To determine the co-localisation of the enzymes responsible for the production of GABA and acetylcholine (which play major roles in the spinal cord) in lamina X of the adult and juvenile mouse, we used a transgenic mouse expressing green fluorescent protein (GFP) in glutamate decarboxylase 67 (GAD67) neurons, combined with choline acetyltransferase (ChAT) immunohistochemistry. ChAT-immunoreactive (IR) and GAD67-GFP containing neurons were observed in lamina X of both adult and juvenile mice and in both age groups a population of cells containing both ChAT-IR and GAD67-GFP were observed in lumbar, thoracic and cervical spinal cord. Such dual labelled cells were predominantly located ventral to the central canal. Immunohistochemistry for vesicular acetylcholine transporter (VAChT) and GAD67 revealed a small number of double labelled terminals located lateral, dorsolateral and ventrolateral to the central canal. This study therefore describes in detail a population of ChAT-IR/GAD67-GFP neurons predominantly ventral to the central canal of the cervical, thoracic and lumbar spinal cord of adult and juvenile mice. These cells potentially correspond to a sub-population of the cholinergic central canal cluster cells which may play a unique role in controlling spinal cord circuitry. |
format | Online Article Text |
id | pubmed-4986852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier/North-Holland Biomedical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49868522016-09-01 Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X Gotts, Jittima Atkinson, Lucy Yanagawa, Yuchio Deuchars, Jim Deuchars, Susan A. Brain Res Research Report Lamina X of the spinal cord is a functionally diverse area with roles in locomotion, autonomic control and processing of mechano and nociceptive information. It is also a neurochemically diverse region. However, the different populations of cells in lamina X remain to be fully characterised. To determine the co-localisation of the enzymes responsible for the production of GABA and acetylcholine (which play major roles in the spinal cord) in lamina X of the adult and juvenile mouse, we used a transgenic mouse expressing green fluorescent protein (GFP) in glutamate decarboxylase 67 (GAD67) neurons, combined with choline acetyltransferase (ChAT) immunohistochemistry. ChAT-immunoreactive (IR) and GAD67-GFP containing neurons were observed in lamina X of both adult and juvenile mice and in both age groups a population of cells containing both ChAT-IR and GAD67-GFP were observed in lumbar, thoracic and cervical spinal cord. Such dual labelled cells were predominantly located ventral to the central canal. Immunohistochemistry for vesicular acetylcholine transporter (VAChT) and GAD67 revealed a small number of double labelled terminals located lateral, dorsolateral and ventrolateral to the central canal. This study therefore describes in detail a population of ChAT-IR/GAD67-GFP neurons predominantly ventral to the central canal of the cervical, thoracic and lumbar spinal cord of adult and juvenile mice. These cells potentially correspond to a sub-population of the cholinergic central canal cluster cells which may play a unique role in controlling spinal cord circuitry. Elsevier/North-Holland Biomedical Press 2016-09-01 /pmc/articles/PMC4986852/ /pubmed/27378584 http://dx.doi.org/10.1016/j.brainres.2016.07.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Report Gotts, Jittima Atkinson, Lucy Yanagawa, Yuchio Deuchars, Jim Deuchars, Susan A. Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X |
title | Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X |
title_full | Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X |
title_fullStr | Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X |
title_full_unstemmed | Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X |
title_short | Co-expression of GAD67 and choline acetyltransferase in neurons in the mouse spinal cord: A focus on lamina X |
title_sort | co-expression of gad67 and choline acetyltransferase in neurons in the mouse spinal cord: a focus on lamina x |
topic | Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986852/ https://www.ncbi.nlm.nih.gov/pubmed/27378584 http://dx.doi.org/10.1016/j.brainres.2016.07.001 |
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