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Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice
Somatostatin (SST)-positive interneurons in the anterior cingulate cortex (ACC) play important roles in neuronal diseases, memory and cognitive functions. However, their development in the ACC remains unclear. Using postnatal day 3 (P3) to P45 GIN mice, we found that most of the intrinsic membrane p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913317/ https://www.ncbi.nlm.nih.gov/pubmed/27319800 http://dx.doi.org/10.1038/srep28137 |
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author | Pan, Geng Yang, Jian-Ming Hu, Xing-Yue Li, Xiao-Ming |
author_facet | Pan, Geng Yang, Jian-Ming Hu, Xing-Yue Li, Xiao-Ming |
author_sort | Pan, Geng |
collection | PubMed |
description | Somatostatin (SST)-positive interneurons in the anterior cingulate cortex (ACC) play important roles in neuronal diseases, memory and cognitive functions. However, their development in the ACC remains unclear. Using postnatal day 3 (P3) to P45 GIN mice, we found that most of the intrinsic membrane properties of SST interneurons in the ACC were developmentally mature after the second postnatal week and that the development of these neurons differed from that of parvalbumin (PV) interneurons in the prefrontal cortex. In addition, electrical coupling between SST interneurons appeared primarily between P12–14. The coupling probability plateaued at approximately P21–30, with a non-age-dependent development of coupling strength. The development of excitatory chemical afferents to SST interneurons occurred earlier than the development of inhibitory chemical afferents. Furthermore, eye closure attenuated the development of electrical coupling probability at P21–30 but had no effect on coupling strength. Eye closure also delayed the development of inhibitory chemical afferent frequency but had no effect on the excitatory chemical afferent amplitude, frequency or rise time. Our data suggest that SST interneurons in the ACC exhibit inherent developmental characteristics distinct from other interneuron subtypes, such as PV interneurons, and that some of these characteristics are subject to environmental regulation. |
format | Online Article Text |
id | pubmed-4913317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49133172016-06-21 Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice Pan, Geng Yang, Jian-Ming Hu, Xing-Yue Li, Xiao-Ming Sci Rep Article Somatostatin (SST)-positive interneurons in the anterior cingulate cortex (ACC) play important roles in neuronal diseases, memory and cognitive functions. However, their development in the ACC remains unclear. Using postnatal day 3 (P3) to P45 GIN mice, we found that most of the intrinsic membrane properties of SST interneurons in the ACC were developmentally mature after the second postnatal week and that the development of these neurons differed from that of parvalbumin (PV) interneurons in the prefrontal cortex. In addition, electrical coupling between SST interneurons appeared primarily between P12–14. The coupling probability plateaued at approximately P21–30, with a non-age-dependent development of coupling strength. The development of excitatory chemical afferents to SST interneurons occurred earlier than the development of inhibitory chemical afferents. Furthermore, eye closure attenuated the development of electrical coupling probability at P21–30 but had no effect on coupling strength. Eye closure also delayed the development of inhibitory chemical afferent frequency but had no effect on the excitatory chemical afferent amplitude, frequency or rise time. Our data suggest that SST interneurons in the ACC exhibit inherent developmental characteristics distinct from other interneuron subtypes, such as PV interneurons, and that some of these characteristics are subject to environmental regulation. Nature Publishing Group 2016-06-20 /pmc/articles/PMC4913317/ /pubmed/27319800 http://dx.doi.org/10.1038/srep28137 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pan, Geng Yang, Jian-Ming Hu, Xing-Yue Li, Xiao-Ming Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
title | Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
title_full | Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
title_fullStr | Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
title_full_unstemmed | Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
title_short | Postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
title_sort | postnatal development of the electrophysiological properties of somatostatin interneurons in the anterior cingulate cortex of mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913317/ https://www.ncbi.nlm.nih.gov/pubmed/27319800 http://dx.doi.org/10.1038/srep28137 |
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