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Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans

Touch deforms, or strains, the skin beyond the immediate point of contact. The spatiotemporal nature of the touch-induced strain fields depend on the mechanical properties of the skin and the tissues below. Somatosensory neurons that sense touch branch out within the skin and rely on a set of mechan...

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Autores principales: Katta, Samata, Sanzeni, Alessandro, Das, Alakananda, Vergassola, Massimo, Goodman, Miriam B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785734/
https://www.ncbi.nlm.nih.gov/pubmed/31533952
http://dx.doi.org/10.1085/jgp.201912374
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author Katta, Samata
Sanzeni, Alessandro
Das, Alakananda
Vergassola, Massimo
Goodman, Miriam B.
author_facet Katta, Samata
Sanzeni, Alessandro
Das, Alakananda
Vergassola, Massimo
Goodman, Miriam B.
author_sort Katta, Samata
collection PubMed
description Touch deforms, or strains, the skin beyond the immediate point of contact. The spatiotemporal nature of the touch-induced strain fields depend on the mechanical properties of the skin and the tissues below. Somatosensory neurons that sense touch branch out within the skin and rely on a set of mechano-electrical transduction channels distributed within their dendrites to detect mechanical stimuli. Here, we sought to understand how tissue mechanics shape touch-induced mechanical strain across the skin over time and how individual channels located in different regions of the strain field contribute to the overall touch response. We leveraged Caenorhabditis elegans’ touch receptor neurons as a simple model amenable to in vivo whole-cell patch-clamp recording and an integrated experimental-computational approach to dissect the mechanisms underlying the spatial and temporal dynamics we observed. Consistent with the idea that strain is produced at a distance, we show that delivering strong stimuli outside the anatomical extent of the neuron is sufficient to evoke MRCs. The amplitude and kinetics of the MRCs depended on both stimulus displacement and speed. Finally, we found that the main factor responsible for touch sensitivity is the recruitment of progressively more distant channels by stronger stimuli, rather than modulation of channel open probability. This principle may generalize to somatosensory neurons with more complex morphologies.
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spelling pubmed-67857342020-04-07 Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans Katta, Samata Sanzeni, Alessandro Das, Alakananda Vergassola, Massimo Goodman, Miriam B. J Gen Physiol Research Articles Touch deforms, or strains, the skin beyond the immediate point of contact. The spatiotemporal nature of the touch-induced strain fields depend on the mechanical properties of the skin and the tissues below. Somatosensory neurons that sense touch branch out within the skin and rely on a set of mechano-electrical transduction channels distributed within their dendrites to detect mechanical stimuli. Here, we sought to understand how tissue mechanics shape touch-induced mechanical strain across the skin over time and how individual channels located in different regions of the strain field contribute to the overall touch response. We leveraged Caenorhabditis elegans’ touch receptor neurons as a simple model amenable to in vivo whole-cell patch-clamp recording and an integrated experimental-computational approach to dissect the mechanisms underlying the spatial and temporal dynamics we observed. Consistent with the idea that strain is produced at a distance, we show that delivering strong stimuli outside the anatomical extent of the neuron is sufficient to evoke MRCs. The amplitude and kinetics of the MRCs depended on both stimulus displacement and speed. Finally, we found that the main factor responsible for touch sensitivity is the recruitment of progressively more distant channels by stronger stimuli, rather than modulation of channel open probability. This principle may generalize to somatosensory neurons with more complex morphologies. Rockefeller University Press 2019-10-07 2019-09-18 /pmc/articles/PMC6785734/ /pubmed/31533952 http://dx.doi.org/10.1085/jgp.201912374 Text en © 2019 Katta et al http://www.rupress.org/termshttps://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms (http://www.rupress.org/terms/) ). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Katta, Samata
Sanzeni, Alessandro
Das, Alakananda
Vergassola, Massimo
Goodman, Miriam B.
Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans
title Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans
title_full Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans
title_fullStr Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans
title_full_unstemmed Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans
title_short Progressive recruitment of distal MEC-4 channels determines touch response strength in C. elegans
title_sort progressive recruitment of distal mec-4 channels determines touch response strength in c. elegans
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785734/
https://www.ncbi.nlm.nih.gov/pubmed/31533952
http://dx.doi.org/10.1085/jgp.201912374
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