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Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb
Proper brain function relies on exquisite balance between excitation and inhibition, where inhibitory circuits play fundamental roles toward sculpting principle neuron output and information processing. In prominent models of olfactory bulb circuitry, inhibition of mitral cells by local interneurons...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584718/ https://www.ncbi.nlm.nih.gov/pubmed/23459611 http://dx.doi.org/10.3389/fncir.2013.00032 |
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author | Huang, Longwen Garcia, Isabella Jen, Hsin-I Arenkiel, Benjamin R. |
author_facet | Huang, Longwen Garcia, Isabella Jen, Hsin-I Arenkiel, Benjamin R. |
author_sort | Huang, Longwen |
collection | PubMed |
description | Proper brain function relies on exquisite balance between excitation and inhibition, where inhibitory circuits play fundamental roles toward sculpting principle neuron output and information processing. In prominent models of olfactory bulb circuitry, inhibition of mitral cells by local interneurons sharpens odor tuning and provides contrast enhancement. Mitral cell inhibition occurs at both mitral cell apical dendrites and deep-layer dendrodendritic synapses between granule cells, the most abundant population of inhibitory interneurons in the olfactory bulb. However, it remains unclear whether other local interneurons make inhibitory connections onto mitral cells. Here, we report a novel circuitry with strong and reciprocal connectivity between a subpopulation of previously uncharacterized Corticotropin-Releasing Hormone (CRH)-expressing interneurons located in the external plexiform layer (EPL), and mitral cells. Using cell type-specific genetic manipulations, imaging, optogenetic stimulation, and electrophysiological recordings, we reveal that CRH-expressing EPL interneurons strongly inhibit mitral cell firing, and that they are reciprocally excited by fast glutamatergic mitral cell input. These findings functionally identify a novel subpopulation of olfactory bulb interneurons that show reciprocal connectivity with mitral cells, uncovering a previously unknown, and potentially critical player in olfactory bulb circuitry that may influence lateral interactions and/or facilitate odor processing. |
format | Online Article Text |
id | pubmed-3584718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35847182013-03-01 Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb Huang, Longwen Garcia, Isabella Jen, Hsin-I Arenkiel, Benjamin R. Front Neural Circuits Neuroscience Proper brain function relies on exquisite balance between excitation and inhibition, where inhibitory circuits play fundamental roles toward sculpting principle neuron output and information processing. In prominent models of olfactory bulb circuitry, inhibition of mitral cells by local interneurons sharpens odor tuning and provides contrast enhancement. Mitral cell inhibition occurs at both mitral cell apical dendrites and deep-layer dendrodendritic synapses between granule cells, the most abundant population of inhibitory interneurons in the olfactory bulb. However, it remains unclear whether other local interneurons make inhibitory connections onto mitral cells. Here, we report a novel circuitry with strong and reciprocal connectivity between a subpopulation of previously uncharacterized Corticotropin-Releasing Hormone (CRH)-expressing interneurons located in the external plexiform layer (EPL), and mitral cells. Using cell type-specific genetic manipulations, imaging, optogenetic stimulation, and electrophysiological recordings, we reveal that CRH-expressing EPL interneurons strongly inhibit mitral cell firing, and that they are reciprocally excited by fast glutamatergic mitral cell input. These findings functionally identify a novel subpopulation of olfactory bulb interneurons that show reciprocal connectivity with mitral cells, uncovering a previously unknown, and potentially critical player in olfactory bulb circuitry that may influence lateral interactions and/or facilitate odor processing. Frontiers Media S.A. 2013-03-01 /pmc/articles/PMC3584718/ /pubmed/23459611 http://dx.doi.org/10.3389/fncir.2013.00032 Text en Copyright © 2013 Huang, Garcia, Jen and Arenkiel. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Neuroscience Huang, Longwen Garcia, Isabella Jen, Hsin-I Arenkiel, Benjamin R. Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
title | Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
title_full | Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
title_fullStr | Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
title_full_unstemmed | Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
title_short | Reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
title_sort | reciprocal connectivity between mitral cells and external plexiform layer interneurons in the mouse olfactory bulb |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584718/ https://www.ncbi.nlm.nih.gov/pubmed/23459611 http://dx.doi.org/10.3389/fncir.2013.00032 |
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