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Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb
The major inhibitory interneurons in olfactory bulb (OB) glomeruli are periglomerular cells (PGCs) and short axon cells (SACs). PGCs and SACs provide feedforward inhibition to all classes of projection neurons, but inhibition between PGCs and SACs is not well understood. We crossed Cre and GFP trans...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565375/ https://www.ncbi.nlm.nih.gov/pubmed/31147391 http://dx.doi.org/10.1523/ENEURO.0048-19.2019 |
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author | Shao, Zuoyi Liu, Shaolin Zhou, Fuwen Puche, Adam C. Shipley, Michael T. |
author_facet | Shao, Zuoyi Liu, Shaolin Zhou, Fuwen Puche, Adam C. Shipley, Michael T. |
author_sort | Shao, Zuoyi |
collection | PubMed |
description | The major inhibitory interneurons in olfactory bulb (OB) glomeruli are periglomerular cells (PGCs) and short axon cells (SACs). PGCs and SACs provide feedforward inhibition to all classes of projection neurons, but inhibition between PGCs and SACs is not well understood. We crossed Cre and GFP transgenic mice and used virally-delivered optogenetic constructs to selectively activate either SACs or GAD65cre-ChR2-positive PGCs while recording from identified GAD65cre-ChR2-positive PGCs or SACs, respectively, to investigate inhibitory interactions between these two interneuron types. We show that GAD65cre-ChR2-positive PGCs robustly inhibit SACs and SACs strongly inhibit PGCs. SACs form the interglomerular circuit, which inhibits PGCs in distant glomeruli. Activation of GAD65cre-ChR2-positive PGCs monosynaptically inhibit mitral cells (MCs), which complements recent findings that SACs directly inhibit MCs. Thus, both classes of glomerular inhibitory neurons inhibit each other, as well as OB output neurons. We further show that olfactory nerve input to one glomerulus engages the interglomerular circuit and inhibits PGCs in distant glomeruli. Sensory activation of the interglomerular circuit directly inhibits output neurons in other glomeruli and by inhibiting intraglomerular PGCs, may potentially disinhibit output neurons in other glomeruli. The nature and context of odorant stimuli may determine whether inhibition or excitation prevails so that odors are represented in part by patterns of active and inactive glomeruli. |
format | Online Article Text |
id | pubmed-6565375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-65653752019-06-18 Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb Shao, Zuoyi Liu, Shaolin Zhou, Fuwen Puche, Adam C. Shipley, Michael T. eNeuro New Research The major inhibitory interneurons in olfactory bulb (OB) glomeruli are periglomerular cells (PGCs) and short axon cells (SACs). PGCs and SACs provide feedforward inhibition to all classes of projection neurons, but inhibition between PGCs and SACs is not well understood. We crossed Cre and GFP transgenic mice and used virally-delivered optogenetic constructs to selectively activate either SACs or GAD65cre-ChR2-positive PGCs while recording from identified GAD65cre-ChR2-positive PGCs or SACs, respectively, to investigate inhibitory interactions between these two interneuron types. We show that GAD65cre-ChR2-positive PGCs robustly inhibit SACs and SACs strongly inhibit PGCs. SACs form the interglomerular circuit, which inhibits PGCs in distant glomeruli. Activation of GAD65cre-ChR2-positive PGCs monosynaptically inhibit mitral cells (MCs), which complements recent findings that SACs directly inhibit MCs. Thus, both classes of glomerular inhibitory neurons inhibit each other, as well as OB output neurons. We further show that olfactory nerve input to one glomerulus engages the interglomerular circuit and inhibits PGCs in distant glomeruli. Sensory activation of the interglomerular circuit directly inhibits output neurons in other glomeruli and by inhibiting intraglomerular PGCs, may potentially disinhibit output neurons in other glomeruli. The nature and context of odorant stimuli may determine whether inhibition or excitation prevails so that odors are represented in part by patterns of active and inactive glomeruli. Society for Neuroscience 2019-06-11 /pmc/articles/PMC6565375/ /pubmed/31147391 http://dx.doi.org/10.1523/ENEURO.0048-19.2019 Text en Copyright © 2019 Shao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Shao, Zuoyi Liu, Shaolin Zhou, Fuwen Puche, Adam C. Shipley, Michael T. Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb |
title | Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb
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title_full | Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb
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title_fullStr | Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb
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title_full_unstemmed | Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb
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title_short | Reciprocal Inhibitory Glomerular Circuits Contribute to Excitation–Inhibition Balance in the Mouse Olfactory Bulb
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title_sort | reciprocal inhibitory glomerular circuits contribute to excitation–inhibition balance in the mouse olfactory bulb |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565375/ https://www.ncbi.nlm.nih.gov/pubmed/31147391 http://dx.doi.org/10.1523/ENEURO.0048-19.2019 |
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