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Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition

The mammalian somatosensory system is comprised of multiple neuronal populations that form specialized, highly organized sensory endings in the skin. The organization of somatosensory endings is essential to their functions, yet the mechanisms which regulate this organization remain unclear. Using a...

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Autores principales: Pomaville, Matthew B., Wright, Kevin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134579/
https://www.ncbi.nlm.nih.gov/pubmed/37106422
http://dx.doi.org/10.1186/s13064-023-00170-2
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author Pomaville, Matthew B.
Wright, Kevin M.
author_facet Pomaville, Matthew B.
Wright, Kevin M.
author_sort Pomaville, Matthew B.
collection PubMed
description The mammalian somatosensory system is comprised of multiple neuronal populations that form specialized, highly organized sensory endings in the skin. The organization of somatosensory endings is essential to their functions, yet the mechanisms which regulate this organization remain unclear. Using a combination of genetic and molecular labeling approaches, we examined the development of mouse hair follicle-innervating low-threshold mechanoreceptors (LTMRs) and explored competition for innervation targets as a mechanism involved in the patterning of their receptive fields. We show that follicle innervating neurons are present in the skin at birth and that LTMR receptive fields gradually add follicle-innervating endings during the first two postnatal weeks. Using a constitutive Bax knockout to increase the number of neurons in adult animals, we show that two LTMR subtypes have differential responses to an increase in neuronal population size: Aδ-LTMR neurons shrink their receptive fields to accommodate the increased number of neurons innervating the skin, while C-LTMR neurons do not. Our findings suggest that competition for hair follicles to innervate plays a role in the patterning and organization of follicle-innervating LTMR neurons. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13064-023-00170-2.
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spelling pubmed-101345792023-04-28 Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition Pomaville, Matthew B. Wright, Kevin M. Neural Dev Research The mammalian somatosensory system is comprised of multiple neuronal populations that form specialized, highly organized sensory endings in the skin. The organization of somatosensory endings is essential to their functions, yet the mechanisms which regulate this organization remain unclear. Using a combination of genetic and molecular labeling approaches, we examined the development of mouse hair follicle-innervating low-threshold mechanoreceptors (LTMRs) and explored competition for innervation targets as a mechanism involved in the patterning of their receptive fields. We show that follicle innervating neurons are present in the skin at birth and that LTMR receptive fields gradually add follicle-innervating endings during the first two postnatal weeks. Using a constitutive Bax knockout to increase the number of neurons in adult animals, we show that two LTMR subtypes have differential responses to an increase in neuronal population size: Aδ-LTMR neurons shrink their receptive fields to accommodate the increased number of neurons innervating the skin, while C-LTMR neurons do not. Our findings suggest that competition for hair follicles to innervate plays a role in the patterning and organization of follicle-innervating LTMR neurons. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13064-023-00170-2. BioMed Central 2023-04-27 /pmc/articles/PMC10134579/ /pubmed/37106422 http://dx.doi.org/10.1186/s13064-023-00170-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Pomaville, Matthew B.
Wright, Kevin M.
Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
title Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
title_full Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
title_fullStr Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
title_full_unstemmed Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
title_short Follicle-innervating Aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
title_sort follicle-innervating aδ-low threshold mechanoreceptive neurons form receptive fields through homotypic competition
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134579/
https://www.ncbi.nlm.nih.gov/pubmed/37106422
http://dx.doi.org/10.1186/s13064-023-00170-2
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