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Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse

In the neocortex, neuronal nitric oxide (NO) synthase (nNOS) is essentially expressed in two classes of GABAergic neurons: type I neurons displaying high levels of expression and type II neurons displaying weaker expression. Using immunocytochemistry in mice expressing GFP under the control of the g...

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Autores principales: Perrenoud, Quentin, Geoffroy, Hélène, Gauthier, Benjamin, Rancillac, Armelle, Alfonsi, Fabienne, Kessaris, Nicoletta, Rossier, Jean, Vitalis, Tania, Gallopin, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386492/
https://www.ncbi.nlm.nih.gov/pubmed/22754499
http://dx.doi.org/10.3389/fncir.2012.00036
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author Perrenoud, Quentin
Geoffroy, Hélène
Gauthier, Benjamin
Rancillac, Armelle
Alfonsi, Fabienne
Kessaris, Nicoletta
Rossier, Jean
Vitalis, Tania
Gallopin, Thierry
author_facet Perrenoud, Quentin
Geoffroy, Hélène
Gauthier, Benjamin
Rancillac, Armelle
Alfonsi, Fabienne
Kessaris, Nicoletta
Rossier, Jean
Vitalis, Tania
Gallopin, Thierry
author_sort Perrenoud, Quentin
collection PubMed
description In the neocortex, neuronal nitric oxide (NO) synthase (nNOS) is essentially expressed in two classes of GABAergic neurons: type I neurons displaying high levels of expression and type II neurons displaying weaker expression. Using immunocytochemistry in mice expressing GFP under the control of the glutamic acid decarboxylase 67k (GAD67) promoter, we studied the distribution of type I and type II neurons in the barrel cortex and their expression of parvalbumin (PV), somatostatin (SOM), and vasoactive intestinal peptide (VIP). We found that type I neurons were predominantly located in deeper layers and expressed SOM (91.5%) while type II neurons were concentrated in layer II/III and VI and expressed PV (17.7%), SOM (18.7%), and VIP (10.2%). We then characterized neurons expressing nNOS mRNA (n = 42 cells) ex vivo, using whole-cell recordings coupled to single-cell reverse transcription-PCR and biocytin labeling. Unsupervised cluster analysis of this sample disclosed four classes. One cluster (n = 7) corresponded to large, deep layer neurons, displaying a high expression of SOM (85.7%) and was thus very likely to correspond to type I neurons. The three other clusters were identified as putative type II cells and corresponded to neurogliaform-like interneurons (n = 19), deep layer neurons expressing PV or SOM (n = 9), and neurons expressing VIP (n = 7). Finally, we performed nNOS immunohistochemistry on mouse lines in which GFP labeling revealed the expression of two specific developmental genes (Lhx6 and 5-HT(3A)). We found that type I neurons expressed Lhx6 but never 5-HT(3A), indicating that they originate in the medial ganglionic eminence (MGE). Type II neurons expressed Lhx6 (63%) and 5-HT(3A) (34.4%) supporting their derivation either from the MGE or from the caudal ganglionic eminence (CGE) and the entopeduncular and dorsal preoptic areas. Together, our results in the barrel cortex of mouse support the view that type I neurons form a specific class of SOM-expressing neurons while type II neurons comprise at least three classes.
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spelling pubmed-33864922012-07-02 Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse Perrenoud, Quentin Geoffroy, Hélène Gauthier, Benjamin Rancillac, Armelle Alfonsi, Fabienne Kessaris, Nicoletta Rossier, Jean Vitalis, Tania Gallopin, Thierry Front Neural Circuits Neuroscience In the neocortex, neuronal nitric oxide (NO) synthase (nNOS) is essentially expressed in two classes of GABAergic neurons: type I neurons displaying high levels of expression and type II neurons displaying weaker expression. Using immunocytochemistry in mice expressing GFP under the control of the glutamic acid decarboxylase 67k (GAD67) promoter, we studied the distribution of type I and type II neurons in the barrel cortex and their expression of parvalbumin (PV), somatostatin (SOM), and vasoactive intestinal peptide (VIP). We found that type I neurons were predominantly located in deeper layers and expressed SOM (91.5%) while type II neurons were concentrated in layer II/III and VI and expressed PV (17.7%), SOM (18.7%), and VIP (10.2%). We then characterized neurons expressing nNOS mRNA (n = 42 cells) ex vivo, using whole-cell recordings coupled to single-cell reverse transcription-PCR and biocytin labeling. Unsupervised cluster analysis of this sample disclosed four classes. One cluster (n = 7) corresponded to large, deep layer neurons, displaying a high expression of SOM (85.7%) and was thus very likely to correspond to type I neurons. The three other clusters were identified as putative type II cells and corresponded to neurogliaform-like interneurons (n = 19), deep layer neurons expressing PV or SOM (n = 9), and neurons expressing VIP (n = 7). Finally, we performed nNOS immunohistochemistry on mouse lines in which GFP labeling revealed the expression of two specific developmental genes (Lhx6 and 5-HT(3A)). We found that type I neurons expressed Lhx6 but never 5-HT(3A), indicating that they originate in the medial ganglionic eminence (MGE). Type II neurons expressed Lhx6 (63%) and 5-HT(3A) (34.4%) supporting their derivation either from the MGE or from the caudal ganglionic eminence (CGE) and the entopeduncular and dorsal preoptic areas. Together, our results in the barrel cortex of mouse support the view that type I neurons form a specific class of SOM-expressing neurons while type II neurons comprise at least three classes. Frontiers Research Foundation 2012-06-29 /pmc/articles/PMC3386492/ /pubmed/22754499 http://dx.doi.org/10.3389/fncir.2012.00036 Text en Copyright © 2012 Perrenoud, Geoffroy, Gauthier, Rancillac, Alfonsi, Kessaris, Rossier, Vitalis and Gallopin. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
Perrenoud, Quentin
Geoffroy, Hélène
Gauthier, Benjamin
Rancillac, Armelle
Alfonsi, Fabienne
Kessaris, Nicoletta
Rossier, Jean
Vitalis, Tania
Gallopin, Thierry
Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
title Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
title_full Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
title_fullStr Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
title_full_unstemmed Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
title_short Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse
title_sort characterization of type i and type ii nnos-expressing interneurons in the barrel cortex of mouse
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386492/
https://www.ncbi.nlm.nih.gov/pubmed/22754499
http://dx.doi.org/10.3389/fncir.2012.00036
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