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Revisiting enigmatic cortical calretinin-expressing interneurons

Cortical calretinin (CR)-expressing interneurons represent a heterogeneous subpopulation of about 10–30% of GABAergic interneurons, which altogether total ca. 12–20% of all cortical neurons. In the rodent neocortex, CR cells display different somatodendritic morphologies ranging from bipolar to mult...

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Autores principales: Cauli, Bruno, Zhou, Xiaojuan, Tricoire, Ludovic, Toussay, Xavier, Staiger, Jochen F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067953/
https://www.ncbi.nlm.nih.gov/pubmed/25009470
http://dx.doi.org/10.3389/fnana.2014.00052
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author Cauli, Bruno
Zhou, Xiaojuan
Tricoire, Ludovic
Toussay, Xavier
Staiger, Jochen F.
author_facet Cauli, Bruno
Zhou, Xiaojuan
Tricoire, Ludovic
Toussay, Xavier
Staiger, Jochen F.
author_sort Cauli, Bruno
collection PubMed
description Cortical calretinin (CR)-expressing interneurons represent a heterogeneous subpopulation of about 10–30% of GABAergic interneurons, which altogether total ca. 12–20% of all cortical neurons. In the rodent neocortex, CR cells display different somatodendritic morphologies ranging from bipolar to multipolar but the bipolar cells and their variations dominate. They are also diverse at the molecular level as they were shown to express numerous neuropeptides in different combinations including vasoactive intestinal polypeptide (VIP), cholecystokinin (CCK), neurokinin B (NKB) corticotrophin releasing factor (CRF), enkephalin (Enk) but also neuropeptide Y (NPY) and somatostatin (SOM) to a lesser extent. CR-expressing interneurons exhibit different firing behaviors such as adapting, bursting or irregular. They mainly originate from the caudal ganglionic eminence (CGE) but a subpopulation also derives from the dorsal part of the medial ganglionic eminence (MGE). Cortical GABAergic CR-expressing interneurons can be divided in two main populations: VIP-bipolar interneurons deriving from the CGE and SOM-Martinotti-like interneurons originating in the dorsal MGE. Although bipolar cells account for the majority of CR-expressing interneurons, the roles they play in cortical neuronal circuits and in the more general metabolic physiology of the brain remained elusive and enigmatic. The aim of this review is, firstly, to provide a comprehensive view of the morphological, molecular and electrophysiological features defining this cell type. We will, secondly, also summarize what is known about their place in the cortical circuit, their modulation by subcortical afferents and the functional roles they might play in neuronal processing and energy metabolism.
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spelling pubmed-40679532014-07-09 Revisiting enigmatic cortical calretinin-expressing interneurons Cauli, Bruno Zhou, Xiaojuan Tricoire, Ludovic Toussay, Xavier Staiger, Jochen F. Front Neuroanat Neuroscience Cortical calretinin (CR)-expressing interneurons represent a heterogeneous subpopulation of about 10–30% of GABAergic interneurons, which altogether total ca. 12–20% of all cortical neurons. In the rodent neocortex, CR cells display different somatodendritic morphologies ranging from bipolar to multipolar but the bipolar cells and their variations dominate. They are also diverse at the molecular level as they were shown to express numerous neuropeptides in different combinations including vasoactive intestinal polypeptide (VIP), cholecystokinin (CCK), neurokinin B (NKB) corticotrophin releasing factor (CRF), enkephalin (Enk) but also neuropeptide Y (NPY) and somatostatin (SOM) to a lesser extent. CR-expressing interneurons exhibit different firing behaviors such as adapting, bursting or irregular. They mainly originate from the caudal ganglionic eminence (CGE) but a subpopulation also derives from the dorsal part of the medial ganglionic eminence (MGE). Cortical GABAergic CR-expressing interneurons can be divided in two main populations: VIP-bipolar interneurons deriving from the CGE and SOM-Martinotti-like interneurons originating in the dorsal MGE. Although bipolar cells account for the majority of CR-expressing interneurons, the roles they play in cortical neuronal circuits and in the more general metabolic physiology of the brain remained elusive and enigmatic. The aim of this review is, firstly, to provide a comprehensive view of the morphological, molecular and electrophysiological features defining this cell type. We will, secondly, also summarize what is known about their place in the cortical circuit, their modulation by subcortical afferents and the functional roles they might play in neuronal processing and energy metabolism. Frontiers Media S.A. 2014-06-24 /pmc/articles/PMC4067953/ /pubmed/25009470 http://dx.doi.org/10.3389/fnana.2014.00052 Text en Copyright © 2014 Cauli, Zhou, Tricoire, Toussay and Staiger. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Cauli, Bruno
Zhou, Xiaojuan
Tricoire, Ludovic
Toussay, Xavier
Staiger, Jochen F.
Revisiting enigmatic cortical calretinin-expressing interneurons
title Revisiting enigmatic cortical calretinin-expressing interneurons
title_full Revisiting enigmatic cortical calretinin-expressing interneurons
title_fullStr Revisiting enigmatic cortical calretinin-expressing interneurons
title_full_unstemmed Revisiting enigmatic cortical calretinin-expressing interneurons
title_short Revisiting enigmatic cortical calretinin-expressing interneurons
title_sort revisiting enigmatic cortical calretinin-expressing interneurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067953/
https://www.ncbi.nlm.nih.gov/pubmed/25009470
http://dx.doi.org/10.3389/fnana.2014.00052
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