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Immunofluorescent visualization of mouse interneuron subtypes
The activity of excitatory neurons is controlled by a highly diverse population of inhibitory interneurons. These cells show a high level of physiological, morphological and neurochemical heterogeneity, and play highly specific roles in neuronal circuits. In the mammalian hippocampus, these are divi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240249/ https://www.ncbi.nlm.nih.gov/pubmed/25469233 http://dx.doi.org/10.12688/f1000research.5349.2 |
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author | Molgaard, Simon Ulrichsen, Maj Boggild, Simon Holm, Marie-Louise Vaegter, Christian Nyengaard, Jens Glerup, Simon |
author_facet | Molgaard, Simon Ulrichsen, Maj Boggild, Simon Holm, Marie-Louise Vaegter, Christian Nyengaard, Jens Glerup, Simon |
author_sort | Molgaard, Simon |
collection | PubMed |
description | The activity of excitatory neurons is controlled by a highly diverse population of inhibitory interneurons. These cells show a high level of physiological, morphological and neurochemical heterogeneity, and play highly specific roles in neuronal circuits. In the mammalian hippocampus, these are divided into 21 different subtypes of GABAergic interneurons based on their expression of different markers, morphology and their electrophysiological properties. Ideally, all can be marked using an antibody directed against the inhibitory neurotransmitter GABA, but parvalbumin, calbindin, somatostatin, and calretinin are also commonly used as markers to narrow down the specific interneuron subtype. Here, we describe a journey to find the necessary immunological reagents for studying GABAergic interneurons of the mouse hippocampus. Based on web searches there are several hundreds of different antibodies on the market directed against these four markers. Searches in the literature databases allowed us to narrow it down to a subset of antibodies most commonly used in publications. However, in our hands the most cited ones did not work for immunofluorescence stainings of formaldehyde fixed tissue sections and cultured hippocampal neurons, and we had to immunostain our way through thirteen different commercial antibodies before finally finding a suitable antibody for each of the four markers. The antibodies were evaluated based on signal-to-noise ratios as well as if positive cells were found in layers of the hippocampus where they have previously been described. Additionally, the antibodies were also tested on sections from mouse spinal cord with similar criteria for specificity of the antibodies. Using the antibodies with a high rating on pAbmAbs, an antibody review database, stainings with high signal-to-noise ratios and location of the immunostained cells in accordance with the literature could be obtained, making these antibodies suitable choices for studying the GABAergic system. |
format | Online Article Text |
id | pubmed-4240249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-42402492014-12-01 Immunofluorescent visualization of mouse interneuron subtypes Molgaard, Simon Ulrichsen, Maj Boggild, Simon Holm, Marie-Louise Vaegter, Christian Nyengaard, Jens Glerup, Simon F1000Res Research Note The activity of excitatory neurons is controlled by a highly diverse population of inhibitory interneurons. These cells show a high level of physiological, morphological and neurochemical heterogeneity, and play highly specific roles in neuronal circuits. In the mammalian hippocampus, these are divided into 21 different subtypes of GABAergic interneurons based on their expression of different markers, morphology and their electrophysiological properties. Ideally, all can be marked using an antibody directed against the inhibitory neurotransmitter GABA, but parvalbumin, calbindin, somatostatin, and calretinin are also commonly used as markers to narrow down the specific interneuron subtype. Here, we describe a journey to find the necessary immunological reagents for studying GABAergic interneurons of the mouse hippocampus. Based on web searches there are several hundreds of different antibodies on the market directed against these four markers. Searches in the literature databases allowed us to narrow it down to a subset of antibodies most commonly used in publications. However, in our hands the most cited ones did not work for immunofluorescence stainings of formaldehyde fixed tissue sections and cultured hippocampal neurons, and we had to immunostain our way through thirteen different commercial antibodies before finally finding a suitable antibody for each of the four markers. The antibodies were evaluated based on signal-to-noise ratios as well as if positive cells were found in layers of the hippocampus where they have previously been described. Additionally, the antibodies were also tested on sections from mouse spinal cord with similar criteria for specificity of the antibodies. Using the antibodies with a high rating on pAbmAbs, an antibody review database, stainings with high signal-to-noise ratios and location of the immunostained cells in accordance with the literature could be obtained, making these antibodies suitable choices for studying the GABAergic system. F1000Research 2014-11-20 /pmc/articles/PMC4240249/ /pubmed/25469233 http://dx.doi.org/10.12688/f1000research.5349.2 Text en Copyright: © 2014 Molgaard S et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Research Note Molgaard, Simon Ulrichsen, Maj Boggild, Simon Holm, Marie-Louise Vaegter, Christian Nyengaard, Jens Glerup, Simon Immunofluorescent visualization of mouse interneuron subtypes |
title | Immunofluorescent visualization of mouse interneuron subtypes |
title_full | Immunofluorescent visualization of mouse interneuron subtypes |
title_fullStr | Immunofluorescent visualization of mouse interneuron subtypes |
title_full_unstemmed | Immunofluorescent visualization of mouse interneuron subtypes |
title_short | Immunofluorescent visualization of mouse interneuron subtypes |
title_sort | immunofluorescent visualization of mouse interneuron subtypes |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240249/ https://www.ncbi.nlm.nih.gov/pubmed/25469233 http://dx.doi.org/10.12688/f1000research.5349.2 |
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