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Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs

Extensive hierarchical yet highly reciprocal interactions among cortical areas are fundamental for information processing. However, connectivity rules governing the specificity of such corticocortical connections, and top-down feedback projections in particular, are poorly understood. We analyze syn...

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Detalles Bibliográficos
Autores principales: Naskar, Shovan, Qi, Jia, Pereira, Francisco, Gerfen, Charles R., Lee, Soohyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995594/
https://www.ncbi.nlm.nih.gov/pubmed/33626343
http://dx.doi.org/10.1016/j.celrep.2021.108774
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author Naskar, Shovan
Qi, Jia
Pereira, Francisco
Gerfen, Charles R.
Lee, Soohyun
author_facet Naskar, Shovan
Qi, Jia
Pereira, Francisco
Gerfen, Charles R.
Lee, Soohyun
author_sort Naskar, Shovan
collection PubMed
description Extensive hierarchical yet highly reciprocal interactions among cortical areas are fundamental for information processing. However, connectivity rules governing the specificity of such corticocortical connections, and top-down feedback projections in particular, are poorly understood. We analyze synaptic strength from functionally relevant brain areas to diverse neuronal types in the primary somatosensory cortex (S1). Long-range projections from different areas preferentially engage specific sets of GABAergic neurons in S1. Projections from other somatosensory cortices strongly recruit parvalbumin (PV)-positive GABAergic neurons and lead to PV neuron-mediated feedforward inhibition of pyramidal neurons in S1. In contrast, inputs from whisker-related primary motor cortex are biased to vasoactive intestinal peptide (VIP)-positive GABAergic neurons and potentially result in VIP neuron-mediated disinhibition. Regardless of the input areas, somatostatin-positive neurons receive relatively weak long-range inputs. Computational analyses suggest that a characteristic combination of synaptic inputs to different GABAergic IN types in S1 represents a specific long-range input area.
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spelling pubmed-79955942021-03-26 Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs Naskar, Shovan Qi, Jia Pereira, Francisco Gerfen, Charles R. Lee, Soohyun Cell Rep Article Extensive hierarchical yet highly reciprocal interactions among cortical areas are fundamental for information processing. However, connectivity rules governing the specificity of such corticocortical connections, and top-down feedback projections in particular, are poorly understood. We analyze synaptic strength from functionally relevant brain areas to diverse neuronal types in the primary somatosensory cortex (S1). Long-range projections from different areas preferentially engage specific sets of GABAergic neurons in S1. Projections from other somatosensory cortices strongly recruit parvalbumin (PV)-positive GABAergic neurons and lead to PV neuron-mediated feedforward inhibition of pyramidal neurons in S1. In contrast, inputs from whisker-related primary motor cortex are biased to vasoactive intestinal peptide (VIP)-positive GABAergic neurons and potentially result in VIP neuron-mediated disinhibition. Regardless of the input areas, somatostatin-positive neurons receive relatively weak long-range inputs. Computational analyses suggest that a characteristic combination of synaptic inputs to different GABAergic IN types in S1 represents a specific long-range input area. 2021-02-23 /pmc/articles/PMC7995594/ /pubmed/33626343 http://dx.doi.org/10.1016/j.celrep.2021.108774 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0).
spellingShingle Article
Naskar, Shovan
Qi, Jia
Pereira, Francisco
Gerfen, Charles R.
Lee, Soohyun
Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs
title Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs
title_full Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs
title_fullStr Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs
title_full_unstemmed Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs
title_short Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs
title_sort cell-type-specific recruitment of gabaergic interneurons in the primary somatosensory cortex by long-range inputs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995594/
https://www.ncbi.nlm.nih.gov/pubmed/33626343
http://dx.doi.org/10.1016/j.celrep.2021.108774
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