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Keratinocytes can modulate and directly initiate nociceptive responses
How thermal, mechanical and chemical stimuli applied to the skin are transduced into signals transmitted by peripheral neurons to the CNS is an area of intense study. Several studies indicate that transduction mechanisms are intrinsic to cutaneous neurons and that epidermal keratinocytes only modula...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576133/ https://www.ncbi.nlm.nih.gov/pubmed/26329459 http://dx.doi.org/10.7554/eLife.09674 |
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author | Baumbauer, Kyle M DeBerry, Jennifer J Adelman, Peter C Miller, Richard H Hachisuka, Junichi Lee, Kuan Hsien Ross, Sarah E Koerber, H Richard Davis, Brian M Albers, Kathryn M |
author_facet | Baumbauer, Kyle M DeBerry, Jennifer J Adelman, Peter C Miller, Richard H Hachisuka, Junichi Lee, Kuan Hsien Ross, Sarah E Koerber, H Richard Davis, Brian M Albers, Kathryn M |
author_sort | Baumbauer, Kyle M |
collection | PubMed |
description | How thermal, mechanical and chemical stimuli applied to the skin are transduced into signals transmitted by peripheral neurons to the CNS is an area of intense study. Several studies indicate that transduction mechanisms are intrinsic to cutaneous neurons and that epidermal keratinocytes only modulate this transduction. Using mice expressing channelrhodopsin (ChR2) in keratinocytes we show that blue light activation of the epidermis alone can produce action potentials (APs) in multiple types of cutaneous sensory neurons including SA1, A-HTMR, CM, CH, CMC, CMH and CMHC fiber types. In loss of function studies, yellow light stimulation of keratinocytes that express halorhodopsin reduced AP generation in response to naturalistic stimuli. These findings support the idea that intrinsic sensory transduction mechanisms in epidermal keratinocytes can directly elicit AP firing in nociceptive as well as tactile sensory afferents and suggest a significantly expanded role for the epidermis in sensory processing. DOI: http://dx.doi.org/10.7554/eLife.09674.001 |
format | Online Article Text |
id | pubmed-4576133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45761332015-09-22 Keratinocytes can modulate and directly initiate nociceptive responses Baumbauer, Kyle M DeBerry, Jennifer J Adelman, Peter C Miller, Richard H Hachisuka, Junichi Lee, Kuan Hsien Ross, Sarah E Koerber, H Richard Davis, Brian M Albers, Kathryn M eLife Neuroscience How thermal, mechanical and chemical stimuli applied to the skin are transduced into signals transmitted by peripheral neurons to the CNS is an area of intense study. Several studies indicate that transduction mechanisms are intrinsic to cutaneous neurons and that epidermal keratinocytes only modulate this transduction. Using mice expressing channelrhodopsin (ChR2) in keratinocytes we show that blue light activation of the epidermis alone can produce action potentials (APs) in multiple types of cutaneous sensory neurons including SA1, A-HTMR, CM, CH, CMC, CMH and CMHC fiber types. In loss of function studies, yellow light stimulation of keratinocytes that express halorhodopsin reduced AP generation in response to naturalistic stimuli. These findings support the idea that intrinsic sensory transduction mechanisms in epidermal keratinocytes can directly elicit AP firing in nociceptive as well as tactile sensory afferents and suggest a significantly expanded role for the epidermis in sensory processing. DOI: http://dx.doi.org/10.7554/eLife.09674.001 eLife Sciences Publications, Ltd 2015-09-02 /pmc/articles/PMC4576133/ /pubmed/26329459 http://dx.doi.org/10.7554/eLife.09674 Text en © 2015, Baumbauer et al 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 Baumbauer, Kyle M DeBerry, Jennifer J Adelman, Peter C Miller, Richard H Hachisuka, Junichi Lee, Kuan Hsien Ross, Sarah E Koerber, H Richard Davis, Brian M Albers, Kathryn M Keratinocytes can modulate and directly initiate nociceptive responses |
title | Keratinocytes can modulate and directly initiate nociceptive responses |
title_full | Keratinocytes can modulate and directly initiate nociceptive responses |
title_fullStr | Keratinocytes can modulate and directly initiate nociceptive responses |
title_full_unstemmed | Keratinocytes can modulate and directly initiate nociceptive responses |
title_short | Keratinocytes can modulate and directly initiate nociceptive responses |
title_sort | keratinocytes can modulate and directly initiate nociceptive responses |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576133/ https://www.ncbi.nlm.nih.gov/pubmed/26329459 http://dx.doi.org/10.7554/eLife.09674 |
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