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Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits

The tachykinin peptide substance P (SP) is expressed by many interneurons and some projection neurons in the superficial dorsal horn of the spinal cord. We have recently shown that SP-expressing excitatory interneurons in lamina II correspond largely to a morphological class known as radial cells. H...

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Autores principales: Polgár, Erika, Bell, Andrew M., Gutierrez-Mecinas, Maria, Dickie, Allen C., Akar, Oğuz, Costreie, Miruna, Watanabe, Masahiko, Todd, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717171/
https://www.ncbi.nlm.nih.gov/pubmed/32634530
http://dx.doi.org/10.1016/j.neuroscience.2020.06.038
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author Polgár, Erika
Bell, Andrew M.
Gutierrez-Mecinas, Maria
Dickie, Allen C.
Akar, Oğuz
Costreie, Miruna
Watanabe, Masahiko
Todd, Andrew J.
author_facet Polgár, Erika
Bell, Andrew M.
Gutierrez-Mecinas, Maria
Dickie, Allen C.
Akar, Oğuz
Costreie, Miruna
Watanabe, Masahiko
Todd, Andrew J.
author_sort Polgár, Erika
collection PubMed
description The tachykinin peptide substance P (SP) is expressed by many interneurons and some projection neurons in the superficial dorsal horn of the spinal cord. We have recently shown that SP-expressing excitatory interneurons in lamina II correspond largely to a morphological class known as radial cells. However, little is known about their function, or their synaptic connectivity. Here we use a modification of the Brainbow technique to define the excitatory synaptic input to SP radial cells. We show that around half of their excitatory synapses (identified by expression of Homer) are from boutons with VGLUT2, which are likely to originate mainly from local interneurons. The remaining synapses presumably include primary afferents, which generally have very low levels of VGLUT2. Our results also suggest that the SP cells are preferentially innervated by a population of excitatory interneurons defined by expression of green fluorescent protein under control of the gene for gastrin-releasing peptide, and that they receive sparser input from other types of excitatory interneuron. We show that around 40% of lamina I projection neurons express Tac1, the gene encoding substance P. Finally, we show that silencing Tac1-expressing cells in the dorsal horn results in a significant reduction in reflex responses to cold and radiant heat, but does not affect withdrawal to von Frey hairs, or chloroquine-evoked itch.
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spelling pubmed-77171712020-12-09 Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits Polgár, Erika Bell, Andrew M. Gutierrez-Mecinas, Maria Dickie, Allen C. Akar, Oğuz Costreie, Miruna Watanabe, Masahiko Todd, Andrew J. Neuroscience Research Article The tachykinin peptide substance P (SP) is expressed by many interneurons and some projection neurons in the superficial dorsal horn of the spinal cord. We have recently shown that SP-expressing excitatory interneurons in lamina II correspond largely to a morphological class known as radial cells. However, little is known about their function, or their synaptic connectivity. Here we use a modification of the Brainbow technique to define the excitatory synaptic input to SP radial cells. We show that around half of their excitatory synapses (identified by expression of Homer) are from boutons with VGLUT2, which are likely to originate mainly from local interneurons. The remaining synapses presumably include primary afferents, which generally have very low levels of VGLUT2. Our results also suggest that the SP cells are preferentially innervated by a population of excitatory interneurons defined by expression of green fluorescent protein under control of the gene for gastrin-releasing peptide, and that they receive sparser input from other types of excitatory interneuron. We show that around 40% of lamina I projection neurons express Tac1, the gene encoding substance P. Finally, we show that silencing Tac1-expressing cells in the dorsal horn results in a significant reduction in reflex responses to cold and radiant heat, but does not affect withdrawal to von Frey hairs, or chloroquine-evoked itch. Elsevier Science 2020-12-01 /pmc/articles/PMC7717171/ /pubmed/32634530 http://dx.doi.org/10.1016/j.neuroscience.2020.06.038 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Polgár, Erika
Bell, Andrew M.
Gutierrez-Mecinas, Maria
Dickie, Allen C.
Akar, Oğuz
Costreie, Miruna
Watanabe, Masahiko
Todd, Andrew J.
Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits
title Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits
title_full Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits
title_fullStr Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits
title_full_unstemmed Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits
title_short Substance P-expressing Neurons in the Superficial Dorsal Horn of the Mouse Spinal Cord: Insights into Their Functions and their Roles in Synaptic Circuits
title_sort substance p-expressing neurons in the superficial dorsal horn of the mouse spinal cord: insights into their functions and their roles in synaptic circuits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717171/
https://www.ncbi.nlm.nih.gov/pubmed/32634530
http://dx.doi.org/10.1016/j.neuroscience.2020.06.038
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