Cargando…

Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors

The human distal limbs have a high spatial acuity for noxious stimuli but a low density of pain-sensing neurites. To elucidate mechanisms underlying regional differences in processing nociception, we sparsely traced non-peptidergic nociceptors across the body using a newly generated Mrgprd(CreERT2)...

Descripción completa

Detalles Bibliográficos
Autores principales: Olson, William, Abdus-Saboor, Ishmail, Cui, Lian, Burdge, Justin, Raabe, Tobias, Ma, Minghong, Luo, Wenqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648527/
https://www.ncbi.nlm.nih.gov/pubmed/29022879
http://dx.doi.org/10.7554/eLife.29507
_version_ 1783272414470209536
author Olson, William
Abdus-Saboor, Ishmail
Cui, Lian
Burdge, Justin
Raabe, Tobias
Ma, Minghong
Luo, Wenqin
author_facet Olson, William
Abdus-Saboor, Ishmail
Cui, Lian
Burdge, Justin
Raabe, Tobias
Ma, Minghong
Luo, Wenqin
author_sort Olson, William
collection PubMed
description The human distal limbs have a high spatial acuity for noxious stimuli but a low density of pain-sensing neurites. To elucidate mechanisms underlying regional differences in processing nociception, we sparsely traced non-peptidergic nociceptors across the body using a newly generated Mrgprd(CreERT2) mouse line. We found that mouse plantar paw skin is also innervated by a low density of Mrgprd(+) nociceptors, while individual arbors in different locations are comparable in size. Surprisingly, the central arbors of plantar paw and trunk innervating nociceptors have distinct morphologies in the spinal cord. This regional difference is well correlated with a heightened signal transmission for plantar paw circuits, as revealed by both spinal cord slice recordings and behavior assays. Taken together, our results elucidate a novel somatotopic functional organization of the mammalian pain system and suggest that regional central arbor structure could facilitate the “enlarged representation” of plantar paw regions in the CNS.
format Online
Article
Text
id pubmed-5648527
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-56485272017-10-23 Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors Olson, William Abdus-Saboor, Ishmail Cui, Lian Burdge, Justin Raabe, Tobias Ma, Minghong Luo, Wenqin eLife Neuroscience The human distal limbs have a high spatial acuity for noxious stimuli but a low density of pain-sensing neurites. To elucidate mechanisms underlying regional differences in processing nociception, we sparsely traced non-peptidergic nociceptors across the body using a newly generated Mrgprd(CreERT2) mouse line. We found that mouse plantar paw skin is also innervated by a low density of Mrgprd(+) nociceptors, while individual arbors in different locations are comparable in size. Surprisingly, the central arbors of plantar paw and trunk innervating nociceptors have distinct morphologies in the spinal cord. This regional difference is well correlated with a heightened signal transmission for plantar paw circuits, as revealed by both spinal cord slice recordings and behavior assays. Taken together, our results elucidate a novel somatotopic functional organization of the mammalian pain system and suggest that regional central arbor structure could facilitate the “enlarged representation” of plantar paw regions in the CNS. eLife Sciences Publications, Ltd 2017-10-12 /pmc/articles/PMC5648527/ /pubmed/29022879 http://dx.doi.org/10.7554/eLife.29507 Text en © 2017, Olson et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Olson, William
Abdus-Saboor, Ishmail
Cui, Lian
Burdge, Justin
Raabe, Tobias
Ma, Minghong
Luo, Wenqin
Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
title Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
title_full Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
title_fullStr Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
title_full_unstemmed Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
title_short Sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
title_sort sparse genetic tracing reveals regionally specific functional organization of mammalian nociceptors
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648527/
https://www.ncbi.nlm.nih.gov/pubmed/29022879
http://dx.doi.org/10.7554/eLife.29507
work_keys_str_mv AT olsonwilliam sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors
AT abdussaboorishmail sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors
AT cuilian sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors
AT burdgejustin sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors
AT raabetobias sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors
AT maminghong sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors
AT luowenqin sparsegenetictracingrevealsregionallyspecificfunctionalorganizationofmammaliannociceptors