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Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn

Parvalbumin-expressing interneurons (PVINs) in the spinal dorsal horn are found primarily in laminae II inner and III. Inhibitory PVINs play an important role in segregating innocuous tactile input from pain-processing circuits through presynaptic inhibition of myelinated low-threshold mechanorecept...

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Autores principales: Gradwell, Mark A., Boyle, Kieran A., Browne, Tyler J., Bell, Andrew M., Leonardo, Jacklyn, Peralta Reyes, Fernanda S., Dickie, Allen C., Smith, Kelly M., Callister, Robert J., Dayas, Christopher V., Hughes, David I., Graham, Brett A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832545/
https://www.ncbi.nlm.nih.gov/pubmed/34326298
http://dx.doi.org/10.1097/j.pain.0000000000002422
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author Gradwell, Mark A.
Boyle, Kieran A.
Browne, Tyler J.
Bell, Andrew M.
Leonardo, Jacklyn
Peralta Reyes, Fernanda S.
Dickie, Allen C.
Smith, Kelly M.
Callister, Robert J.
Dayas, Christopher V.
Hughes, David I.
Graham, Brett A.
author_facet Gradwell, Mark A.
Boyle, Kieran A.
Browne, Tyler J.
Bell, Andrew M.
Leonardo, Jacklyn
Peralta Reyes, Fernanda S.
Dickie, Allen C.
Smith, Kelly M.
Callister, Robert J.
Dayas, Christopher V.
Hughes, David I.
Graham, Brett A.
author_sort Gradwell, Mark A.
collection PubMed
description Parvalbumin-expressing interneurons (PVINs) in the spinal dorsal horn are found primarily in laminae II inner and III. Inhibitory PVINs play an important role in segregating innocuous tactile input from pain-processing circuits through presynaptic inhibition of myelinated low-threshold mechanoreceptors and postsynaptic inhibition of distinct spinal circuits. By comparison, relatively little is known of the role of excitatory PVINs (ePVINs) in sensory processing. Here, we use neuroanatomical and optogenetic approaches to show that ePVINs comprise a larger proportion of the PVIN population than previously reported and that both ePVIN and inhibitory PVIN populations form synaptic connections among (and between) themselves. We find that these cells contribute to neuronal networks that influence activity within several functionally distinct circuits and that aberrant activity of ePVINs under pathological conditions is well placed to contribute to the development of mechanical hypersensitivity.
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spelling pubmed-88325452022-02-17 Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn Gradwell, Mark A. Boyle, Kieran A. Browne, Tyler J. Bell, Andrew M. Leonardo, Jacklyn Peralta Reyes, Fernanda S. Dickie, Allen C. Smith, Kelly M. Callister, Robert J. Dayas, Christopher V. Hughes, David I. Graham, Brett A. Pain Research Paper Parvalbumin-expressing interneurons (PVINs) in the spinal dorsal horn are found primarily in laminae II inner and III. Inhibitory PVINs play an important role in segregating innocuous tactile input from pain-processing circuits through presynaptic inhibition of myelinated low-threshold mechanoreceptors and postsynaptic inhibition of distinct spinal circuits. By comparison, relatively little is known of the role of excitatory PVINs (ePVINs) in sensory processing. Here, we use neuroanatomical and optogenetic approaches to show that ePVINs comprise a larger proportion of the PVIN population than previously reported and that both ePVIN and inhibitory PVIN populations form synaptic connections among (and between) themselves. We find that these cells contribute to neuronal networks that influence activity within several functionally distinct circuits and that aberrant activity of ePVINs under pathological conditions is well placed to contribute to the development of mechanical hypersensitivity. Wolters Kluwer 2022-03 2021-07-28 /pmc/articles/PMC8832545/ /pubmed/34326298 http://dx.doi.org/10.1097/j.pain.0000000000002422 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Gradwell, Mark A.
Boyle, Kieran A.
Browne, Tyler J.
Bell, Andrew M.
Leonardo, Jacklyn
Peralta Reyes, Fernanda S.
Dickie, Allen C.
Smith, Kelly M.
Callister, Robert J.
Dayas, Christopher V.
Hughes, David I.
Graham, Brett A.
Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
title Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
title_full Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
title_fullStr Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
title_full_unstemmed Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
title_short Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
title_sort diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832545/
https://www.ncbi.nlm.nih.gov/pubmed/34326298
http://dx.doi.org/10.1097/j.pain.0000000000002422
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