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Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences

In the human neocortex coherent interlaminar theta oscillations are driven by deep cortical layers, suggesting neurons in these layers exhibit distinct electrophysiological properties. To characterize this potential distinctiveness, we use in vitro whole-cell recordings from cortical layers 2 and 3...

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Autores principales: Moradi Chameh, Homeira, Rich, Scott, Wang, Lihua, Chen, Fu-Der, Zhang, Liang, Carlen, Peter L., Tripathy, Shreejoy J., Valiante, Taufik A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093195/
https://www.ncbi.nlm.nih.gov/pubmed/33941783
http://dx.doi.org/10.1038/s41467-021-22741-9
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author Moradi Chameh, Homeira
Rich, Scott
Wang, Lihua
Chen, Fu-Der
Zhang, Liang
Carlen, Peter L.
Tripathy, Shreejoy J.
Valiante, Taufik A.
author_facet Moradi Chameh, Homeira
Rich, Scott
Wang, Lihua
Chen, Fu-Der
Zhang, Liang
Carlen, Peter L.
Tripathy, Shreejoy J.
Valiante, Taufik A.
author_sort Moradi Chameh, Homeira
collection PubMed
description In the human neocortex coherent interlaminar theta oscillations are driven by deep cortical layers, suggesting neurons in these layers exhibit distinct electrophysiological properties. To characterize this potential distinctiveness, we use in vitro whole-cell recordings from cortical layers 2 and 3 (L2&3), layer 3c (L3c) and layer 5 (L5) of the human cortex. Across all layers we observe notable heterogeneity, indicating human cortical pyramidal neurons are an electrophysiologically diverse population. L5 pyramidal cells are the most excitable of these neurons and exhibit the most prominent sag current (abolished by blockade of the hyperpolarization activated cation current, I(h)). While subthreshold resonance is more common in L3c and L5, we rarely observe this resonance at frequencies greater than 2 Hz. However, the frequency dependent gain of L5 neurons reveals they are most adept at tracking both delta and theta frequency inputs, a unique feature that may indirectly be important for the generation of cortical theta oscillations.
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spelling pubmed-80931952021-05-11 Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences Moradi Chameh, Homeira Rich, Scott Wang, Lihua Chen, Fu-Der Zhang, Liang Carlen, Peter L. Tripathy, Shreejoy J. Valiante, Taufik A. Nat Commun Article In the human neocortex coherent interlaminar theta oscillations are driven by deep cortical layers, suggesting neurons in these layers exhibit distinct electrophysiological properties. To characterize this potential distinctiveness, we use in vitro whole-cell recordings from cortical layers 2 and 3 (L2&3), layer 3c (L3c) and layer 5 (L5) of the human cortex. Across all layers we observe notable heterogeneity, indicating human cortical pyramidal neurons are an electrophysiologically diverse population. L5 pyramidal cells are the most excitable of these neurons and exhibit the most prominent sag current (abolished by blockade of the hyperpolarization activated cation current, I(h)). While subthreshold resonance is more common in L3c and L5, we rarely observe this resonance at frequencies greater than 2 Hz. However, the frequency dependent gain of L5 neurons reveals they are most adept at tracking both delta and theta frequency inputs, a unique feature that may indirectly be important for the generation of cortical theta oscillations. Nature Publishing Group UK 2021-05-03 /pmc/articles/PMC8093195/ /pubmed/33941783 http://dx.doi.org/10.1038/s41467-021-22741-9 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Moradi Chameh, Homeira
Rich, Scott
Wang, Lihua
Chen, Fu-Der
Zhang, Liang
Carlen, Peter L.
Tripathy, Shreejoy J.
Valiante, Taufik A.
Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
title Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
title_full Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
title_fullStr Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
title_full_unstemmed Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
title_short Diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
title_sort diversity amongst human cortical pyramidal neurons revealed via their sag currents and frequency preferences
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093195/
https://www.ncbi.nlm.nih.gov/pubmed/33941783
http://dx.doi.org/10.1038/s41467-021-22741-9
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