Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Molgaard, Simon, Ulrichsen, Maj, Boggild, Simon, Holm, Marie-Louise, Vaegter, Christian, Nyengaard, Jens, Glerup, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2014
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
_version_ 1782345702990413824
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
work_keys_str_mv AT molgaardsimon immunofluorescentvisualizationofmouseinterneuronsubtypes
AT ulrichsenmaj immunofluorescentvisualizationofmouseinterneuronsubtypes
AT boggildsimon immunofluorescentvisualizationofmouseinterneuronsubtypes
AT holmmarielouise immunofluorescentvisualizationofmouseinterneuronsubtypes
AT vaegterchristian immunofluorescentvisualizationofmouseinterneuronsubtypes
AT nyengaardjens immunofluorescentvisualizationofmouseinterneuronsubtypes
AT glerupsimon immunofluorescentvisualizationofmouseinterneuronsubtypes