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Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex

Inhibitory interneurons make up around 10–20% of the total neuron population in the cerebral cortex. A hallmark of inhibitory interneurons is their remarkable diversity in terms of morphology, synaptic connectivity, electrophysiological and neurochemical properties. It is generally understood that t...

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Detalles Bibliográficos
Autor principal: Riedemann, Therese
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627222/
https://www.ncbi.nlm.nih.gov/pubmed/31212931
http://dx.doi.org/10.3390/ijms20122952
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author Riedemann, Therese
author_facet Riedemann, Therese
author_sort Riedemann, Therese
collection PubMed
description Inhibitory interneurons make up around 10–20% of the total neuron population in the cerebral cortex. A hallmark of inhibitory interneurons is their remarkable diversity in terms of morphology, synaptic connectivity, electrophysiological and neurochemical properties. It is generally understood that there are three distinct and non-overlapping interneuron classes in the mouse neocortex, namely, parvalbumin-expressing, 5-HT(3A) receptor-expressing and somatostatin-expressing interneuron classes. Each class is, in turn, composed of a multitude of subclasses, resulting in a growing number of interneuron classes and subclasses. In this review, I will focus on the diversity of somatostatin-expressing interneurons (SOM(+) INs) in the cerebral cortex and elucidate their function in cortical circuits. I will then discuss pathological consequences of a malfunctioning of SOM(+) INs in neurological disorders such as major depressive disorder, and present future avenues in SOM research and brain pathologies.
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spelling pubmed-66272222019-07-23 Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex Riedemann, Therese Int J Mol Sci Review Inhibitory interneurons make up around 10–20% of the total neuron population in the cerebral cortex. A hallmark of inhibitory interneurons is their remarkable diversity in terms of morphology, synaptic connectivity, electrophysiological and neurochemical properties. It is generally understood that there are three distinct and non-overlapping interneuron classes in the mouse neocortex, namely, parvalbumin-expressing, 5-HT(3A) receptor-expressing and somatostatin-expressing interneuron classes. Each class is, in turn, composed of a multitude of subclasses, resulting in a growing number of interneuron classes and subclasses. In this review, I will focus on the diversity of somatostatin-expressing interneurons (SOM(+) INs) in the cerebral cortex and elucidate their function in cortical circuits. I will then discuss pathological consequences of a malfunctioning of SOM(+) INs in neurological disorders such as major depressive disorder, and present future avenues in SOM research and brain pathologies. MDPI 2019-06-17 /pmc/articles/PMC6627222/ /pubmed/31212931 http://dx.doi.org/10.3390/ijms20122952 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Riedemann, Therese
Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex
title Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex
title_full Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex
title_fullStr Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex
title_full_unstemmed Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex
title_short Diversity and Function of Somatostatin-Expressing Interneurons in the Cerebral Cortex
title_sort diversity and function of somatostatin-expressing interneurons in the cerebral cortex
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627222/
https://www.ncbi.nlm.nih.gov/pubmed/31212931
http://dx.doi.org/10.3390/ijms20122952
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