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Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors
Touch submodalities, such as flutter and pressure, are mediated by somatosensory afferents whose terminal specializations extract tactile features and encode them as action potential trains with unique activity patterns(1). Whether non-neuronal cells tune touch receptors through active or passive me...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4097312/ https://www.ncbi.nlm.nih.gov/pubmed/24717432 http://dx.doi.org/10.1038/nature13250 |
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author | Maksimovic, Srdjan Nakatani, Masashi Baba, Yoshichika Nelson, Aislyn M. Marshall, Kara L. Wellnitz, Scott A. Firozi, Pervez Woo, Seung-Hyun Ranade, Sanjeev Patapoutian, Ardem Lumpkin, Ellen A. |
author_facet | Maksimovic, Srdjan Nakatani, Masashi Baba, Yoshichika Nelson, Aislyn M. Marshall, Kara L. Wellnitz, Scott A. Firozi, Pervez Woo, Seung-Hyun Ranade, Sanjeev Patapoutian, Ardem Lumpkin, Ellen A. |
author_sort | Maksimovic, Srdjan |
collection | PubMed |
description | Touch submodalities, such as flutter and pressure, are mediated by somatosensory afferents whose terminal specializations extract tactile features and encode them as action potential trains with unique activity patterns(1). Whether non-neuronal cells tune touch receptors through active or passive mechanisms is debated. Terminal specializations are thought to function as passive mechanical filters analogous to the cochlea’s basilar membrane, which deconstructs complex sounds into tones that are transduced by mechanosensory hair cells. The model that cutaneous specializations are merely passive has been recently challenged because epidermal cells express sensory ion channels and neurotransmitters(2,3); however, direct evidence that epidermal cells excite tactile afferents is lacking. Epidermal Merkel cells display features of sensory receptor cells(4,5) and make “synapse-like” contacts(5,6) with slowly adapting type I (SAI) afferents(7–9). These complexes, which encode spatial features such as edges and texture(1), localize to skin regions with high tactile acuity, including whisker follicles, fingertips and touch domes. Here, we show that Merkel cells actively participate in touch reception in mice. First, Merkel cells display fast, touch-evoked mechanotransduction currents. Second, optogenetic approaches in intact skin show that Merkel cells are both necessary and sufficient for sustained action-potential firing in tactile afferents. Third, recordings from touch-dome afferents lacking Merkel cells demonstrate that Merkel cells confer high-frequency responses to dynamic stimuli and enable sustained firing. These data are the first to directly demonstrate a functional, excitatory connection between epidermal cells and sensory neurons. Together, these findings indicate that Merkel cells actively tune mechanosensory responses to facilitate high spatio-temporal acuity. Moreover, our results suggest a division of labour in the Merkel cell-neurite complex: Merkel cells signal static stimuli, such as pressure, whereas sensory afferents transduce dynamic stimuli, such as moving gratings. Thus, the Merkel-cell neurite complex is unique sensory structure with two receptor cell types specialized for distinct elements of discriminative touch. |
format | Online Article Text |
id | pubmed-4097312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-40973122014-11-29 Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors Maksimovic, Srdjan Nakatani, Masashi Baba, Yoshichika Nelson, Aislyn M. Marshall, Kara L. Wellnitz, Scott A. Firozi, Pervez Woo, Seung-Hyun Ranade, Sanjeev Patapoutian, Ardem Lumpkin, Ellen A. Nature Article Touch submodalities, such as flutter and pressure, are mediated by somatosensory afferents whose terminal specializations extract tactile features and encode them as action potential trains with unique activity patterns(1). Whether non-neuronal cells tune touch receptors through active or passive mechanisms is debated. Terminal specializations are thought to function as passive mechanical filters analogous to the cochlea’s basilar membrane, which deconstructs complex sounds into tones that are transduced by mechanosensory hair cells. The model that cutaneous specializations are merely passive has been recently challenged because epidermal cells express sensory ion channels and neurotransmitters(2,3); however, direct evidence that epidermal cells excite tactile afferents is lacking. Epidermal Merkel cells display features of sensory receptor cells(4,5) and make “synapse-like” contacts(5,6) with slowly adapting type I (SAI) afferents(7–9). These complexes, which encode spatial features such as edges and texture(1), localize to skin regions with high tactile acuity, including whisker follicles, fingertips and touch domes. Here, we show that Merkel cells actively participate in touch reception in mice. First, Merkel cells display fast, touch-evoked mechanotransduction currents. Second, optogenetic approaches in intact skin show that Merkel cells are both necessary and sufficient for sustained action-potential firing in tactile afferents. Third, recordings from touch-dome afferents lacking Merkel cells demonstrate that Merkel cells confer high-frequency responses to dynamic stimuli and enable sustained firing. These data are the first to directly demonstrate a functional, excitatory connection between epidermal cells and sensory neurons. Together, these findings indicate that Merkel cells actively tune mechanosensory responses to facilitate high spatio-temporal acuity. Moreover, our results suggest a division of labour in the Merkel cell-neurite complex: Merkel cells signal static stimuli, such as pressure, whereas sensory afferents transduce dynamic stimuli, such as moving gratings. Thus, the Merkel-cell neurite complex is unique sensory structure with two receptor cell types specialized for distinct elements of discriminative touch. 2014-04-06 2014-05-29 /pmc/articles/PMC4097312/ /pubmed/24717432 http://dx.doi.org/10.1038/nature13250 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Maksimovic, Srdjan Nakatani, Masashi Baba, Yoshichika Nelson, Aislyn M. Marshall, Kara L. Wellnitz, Scott A. Firozi, Pervez Woo, Seung-Hyun Ranade, Sanjeev Patapoutian, Ardem Lumpkin, Ellen A. Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors |
title | Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors |
title_full | Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors |
title_fullStr | Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors |
title_full_unstemmed | Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors |
title_short | Epidermal Merkel Cells are Mechanosensory Cells that Tune Mammalian Touch Receptors |
title_sort | epidermal merkel cells are mechanosensory cells that tune mammalian touch receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4097312/ https://www.ncbi.nlm.nih.gov/pubmed/24717432 http://dx.doi.org/10.1038/nature13250 |
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