Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.

Back pain and intervertebral disc degeneration are prevalent, costly, and widely treated by manual therapies, yet the underlying causes of these diseases are indeterminate as are the scientific bases for such treatments. The present studies characterize the effects of repetitive in vivo manual loads...

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Main Authors: John Robert Matyas, Claudia Klein, Dragana Ponjevic, Neil A Duncan, Gregory N Kawchuk
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0248104
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spelling doaj-8cb0e6c8707d489687dd64799509fc262021-04-07T04:32:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01163e024810410.1371/journal.pone.0248104Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.John Robert MatyasClaudia KleinDragana PonjevicNeil A DuncanGregory N KawchukBack pain and intervertebral disc degeneration are prevalent, costly, and widely treated by manual therapies, yet the underlying causes of these diseases are indeterminate as are the scientific bases for such treatments. The present studies characterize the effects of repetitive in vivo manual loads on porcine intervertebral disc cell metabolism using RNA deep sequencing. A single session of repetitive manual loading applied to the lumbar spine induced both up- and down-regulation of a variety of genes transcribed by cells in the ventral annuli fibrosi. The effect of manual therapy at the level of loading was greater than at a level distant to the applied load. Gene ontology and molecular pathway analyses categorized biological, molecular, and cellular functions influenced by repetitive manual loading, with over-representation of membrane, transmembrane, and pericellular activities. Weighted Gene Co-expression Network Analysis discerned enrichment in genes in pathways of inflammation and skeletogenesis. The present studies support previous findings of intervertebral disc cell mechanotransduction, and are the first to report comprehensively on the repertoire of gene targets influenced by mechanical loads associated with manual therapy interventions. The present study defines the cellular response of repeated, low-amplitude loads on normal healthy annuli fibrosi and lays the foundation for future work defining how healthy and diseased intervertebral discs respond to single or low-frequency manual loads typical of those applied clinically.https://doi.org/10.1371/journal.pone.0248104
collection DOAJ
language English
format Article
sources DOAJ
author John Robert Matyas
Claudia Klein
Dragana Ponjevic
Neil A Duncan
Gregory N Kawchuk
spellingShingle John Robert Matyas
Claudia Klein
Dragana Ponjevic
Neil A Duncan
Gregory N Kawchuk
Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
PLoS ONE
author_facet John Robert Matyas
Claudia Klein
Dragana Ponjevic
Neil A Duncan
Gregory N Kawchuk
author_sort John Robert Matyas
title Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
title_short Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
title_full Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
title_fullStr Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
title_full_unstemmed Repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
title_sort repetitive in vivo manual loading of the spine elicits cellular responses in porcine annuli fibrosi.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Back pain and intervertebral disc degeneration are prevalent, costly, and widely treated by manual therapies, yet the underlying causes of these diseases are indeterminate as are the scientific bases for such treatments. The present studies characterize the effects of repetitive in vivo manual loads on porcine intervertebral disc cell metabolism using RNA deep sequencing. A single session of repetitive manual loading applied to the lumbar spine induced both up- and down-regulation of a variety of genes transcribed by cells in the ventral annuli fibrosi. The effect of manual therapy at the level of loading was greater than at a level distant to the applied load. Gene ontology and molecular pathway analyses categorized biological, molecular, and cellular functions influenced by repetitive manual loading, with over-representation of membrane, transmembrane, and pericellular activities. Weighted Gene Co-expression Network Analysis discerned enrichment in genes in pathways of inflammation and skeletogenesis. The present studies support previous findings of intervertebral disc cell mechanotransduction, and are the first to report comprehensively on the repertoire of gene targets influenced by mechanical loads associated with manual therapy interventions. The present study defines the cellular response of repeated, low-amplitude loads on normal healthy annuli fibrosi and lays the foundation for future work defining how healthy and diseased intervertebral discs respond to single or low-frequency manual loads typical of those applied clinically.
url https://doi.org/10.1371/journal.pone.0248104
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