Cargando…
Functional analysis of human intrafusal fiber innervation by human γ-motoneurons
Investigation of neuromuscular deficits and diseases such as SMA, as well as for next generation prosthetics, utilizing in vitro phenotypic models would benefit from the development of a functional neuromuscular reflex arc. The neuromuscular reflex arc is the system that integrates the proprioceptiv...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722897/ https://www.ncbi.nlm.nih.gov/pubmed/29222416 http://dx.doi.org/10.1038/s41598-017-17382-2 |
_version_ | 1783285099632001024 |
---|---|
author | Colón, A. Guo, X. Akanda, N. Cai, Y. Hickman, J. J. |
author_facet | Colón, A. Guo, X. Akanda, N. Cai, Y. Hickman, J. J. |
author_sort | Colón, A. |
collection | PubMed |
description | Investigation of neuromuscular deficits and diseases such as SMA, as well as for next generation prosthetics, utilizing in vitro phenotypic models would benefit from the development of a functional neuromuscular reflex arc. The neuromuscular reflex arc is the system that integrates the proprioceptive information for muscle length and activity (sensory afferent), to modify motoneuron output to achieve graded muscle contraction (actuation efferent). The sensory portion of the arc is composed of proprioceptive sensory neurons and the muscle spindle, which is embedded in the muscle tissue and composed of intrafusal fibers. The gamma motoneurons (γ-MNs) that innervate these fibers regulate the intrafusal fiber’s stretch so that they retain proper tension and sensitivity during muscle contraction or relaxation. This mechanism is in place to maintain the sensitivity of proprioception during dynamic muscle activity and to prevent muscular damage. In this study, a co-culture system was developed for innervation of intrafusal fibers by human γ-MNs and demonstrated by morphological and immunocytochemical analysis, then validated by functional electrophysiological evaluation. This human-based fusimotor model and its incorporation into the reflex arc allows for a more accurate recapitulation of neuromuscular function for applications in disease investigations, drug discovery, prosthetic design and neuropathic pain investigations. |
format | Online Article Text |
id | pubmed-5722897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57228972017-12-12 Functional analysis of human intrafusal fiber innervation by human γ-motoneurons Colón, A. Guo, X. Akanda, N. Cai, Y. Hickman, J. J. Sci Rep Article Investigation of neuromuscular deficits and diseases such as SMA, as well as for next generation prosthetics, utilizing in vitro phenotypic models would benefit from the development of a functional neuromuscular reflex arc. The neuromuscular reflex arc is the system that integrates the proprioceptive information for muscle length and activity (sensory afferent), to modify motoneuron output to achieve graded muscle contraction (actuation efferent). The sensory portion of the arc is composed of proprioceptive sensory neurons and the muscle spindle, which is embedded in the muscle tissue and composed of intrafusal fibers. The gamma motoneurons (γ-MNs) that innervate these fibers regulate the intrafusal fiber’s stretch so that they retain proper tension and sensitivity during muscle contraction or relaxation. This mechanism is in place to maintain the sensitivity of proprioception during dynamic muscle activity and to prevent muscular damage. In this study, a co-culture system was developed for innervation of intrafusal fibers by human γ-MNs and demonstrated by morphological and immunocytochemical analysis, then validated by functional electrophysiological evaluation. This human-based fusimotor model and its incorporation into the reflex arc allows for a more accurate recapitulation of neuromuscular function for applications in disease investigations, drug discovery, prosthetic design and neuropathic pain investigations. Nature Publishing Group UK 2017-12-08 /pmc/articles/PMC5722897/ /pubmed/29222416 http://dx.doi.org/10.1038/s41598-017-17382-2 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Colón, A. Guo, X. Akanda, N. Cai, Y. Hickman, J. J. Functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
title | Functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
title_full | Functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
title_fullStr | Functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
title_full_unstemmed | Functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
title_short | Functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
title_sort | functional analysis of human intrafusal fiber innervation by human γ-motoneurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722897/ https://www.ncbi.nlm.nih.gov/pubmed/29222416 http://dx.doi.org/10.1038/s41598-017-17382-2 |
work_keys_str_mv | AT colona functionalanalysisofhumanintrafusalfiberinnervationbyhumangmotoneurons AT guox functionalanalysisofhumanintrafusalfiberinnervationbyhumangmotoneurons AT akandan functionalanalysisofhumanintrafusalfiberinnervationbyhumangmotoneurons AT caiy functionalanalysisofhumanintrafusalfiberinnervationbyhumangmotoneurons AT hickmanjj functionalanalysisofhumanintrafusalfiberinnervationbyhumangmotoneurons |