The role of transient receptor potential channels in joint diseases

ransient receptor potential channels (TRP channels) are cation selective transmembrane receptors with diverse structures, activation mechanisms and physiological functions. TRP channels act as cellular sensors for a plethora of stimuli, including temperature, membrane voltage, oxidative stress, mech...

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Main Authors: O Krupkova, J Zvick, K Wuertz-Kozak
Format: Article
Language:English
Published: AO Research Institute Davos 2017-10-01
Series:European Cells & Materials
Subjects:
Online Access:http://www.ecmjournal.org/papers/vol034/pdf/v034a12.pdf
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spelling doaj-2ec0fe34527543ff81ab669878469b2c2020-11-25T00:55:12Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622017-10-013418020110.22203/eCM.v034a12The role of transient receptor potential channels in joint diseasesO Krupkova0J Zvick K Wuertz-KozakETH Zurich, Hoenggerbergring 64, 8093 Zurich, Switzerlandransient receptor potential channels (TRP channels) are cation selective transmembrane receptors with diverse structures, activation mechanisms and physiological functions. TRP channels act as cellular sensors for a plethora of stimuli, including temperature, membrane voltage, oxidative stress, mechanical stimuli, pH and endogenous, as well as, exogenous ligands, thereby illustrating their versatility. As such, TRP channels regulate various functions in both excitable and non-excitable cells, mainly by mediating Ca2+ homeostasis. Dysregulation of TRP channels is implicated in many pathologies, including cardiovascular diseases, muscular dystrophies and hyperalgesia. However, the importance of TRP channel expression, physiological function and regulation in chondrocytes and intervertebral disc (IVD) cells is largely unexplored. Osteoarthritis (OA) and degenerative disc disease (DDD) are chronic age-related disorders that significantly affect the quality of life by causing pain, activity limitation and disability. Furthermore, currently available therapies cannot effectively slow-down or stop progression of these diseases. Both OA and DDD are characterised by reduced tissue cellularity, enhanced inflammatory responses and molecular, structural and mechanical alterations of the extracellular matrix, hence affecting load distribution and reducing joint flexibility. However, knowledge on how chondrocytes and IVD cells sense their microenvironment and respond to its changes is still limited. In this review, we introduced six families of mammalian TRP channels, their mechanisms of activation, as well as, activation-driven cellular consequences. We summarised the current knowledge on TRP channel expression and activity in chondrocytes and IVD cells, as well as, the significance of TRP channels as therapeutic targets for the treatment of OA and DDD.http://www.ecmjournal.org/papers/vol034/pdf/v034a12.pdfTransient receptor potential channelsdegenerative disc diseaseosteoarthritisnociceptionmechanosensingosmosensinginflammationcalcium
collection DOAJ
language English
format Article
sources DOAJ
author O Krupkova
J Zvick
K Wuertz-Kozak
spellingShingle O Krupkova
J Zvick
K Wuertz-Kozak
The role of transient receptor potential channels in joint diseases
European Cells & Materials
Transient receptor potential channels
degenerative disc disease
osteoarthritis
nociception
mechanosensing
osmosensing
inflammation
calcium
author_facet O Krupkova
J Zvick
K Wuertz-Kozak
author_sort O Krupkova
title The role of transient receptor potential channels in joint diseases
title_short The role of transient receptor potential channels in joint diseases
title_full The role of transient receptor potential channels in joint diseases
title_fullStr The role of transient receptor potential channels in joint diseases
title_full_unstemmed The role of transient receptor potential channels in joint diseases
title_sort role of transient receptor potential channels in joint diseases
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2017-10-01
description ransient receptor potential channels (TRP channels) are cation selective transmembrane receptors with diverse structures, activation mechanisms and physiological functions. TRP channels act as cellular sensors for a plethora of stimuli, including temperature, membrane voltage, oxidative stress, mechanical stimuli, pH and endogenous, as well as, exogenous ligands, thereby illustrating their versatility. As such, TRP channels regulate various functions in both excitable and non-excitable cells, mainly by mediating Ca2+ homeostasis. Dysregulation of TRP channels is implicated in many pathologies, including cardiovascular diseases, muscular dystrophies and hyperalgesia. However, the importance of TRP channel expression, physiological function and regulation in chondrocytes and intervertebral disc (IVD) cells is largely unexplored. Osteoarthritis (OA) and degenerative disc disease (DDD) are chronic age-related disorders that significantly affect the quality of life by causing pain, activity limitation and disability. Furthermore, currently available therapies cannot effectively slow-down or stop progression of these diseases. Both OA and DDD are characterised by reduced tissue cellularity, enhanced inflammatory responses and molecular, structural and mechanical alterations of the extracellular matrix, hence affecting load distribution and reducing joint flexibility. However, knowledge on how chondrocytes and IVD cells sense their microenvironment and respond to its changes is still limited. In this review, we introduced six families of mammalian TRP channels, their mechanisms of activation, as well as, activation-driven cellular consequences. We summarised the current knowledge on TRP channel expression and activity in chondrocytes and IVD cells, as well as, the significance of TRP channels as therapeutic targets for the treatment of OA and DDD.
topic Transient receptor potential channels
degenerative disc disease
osteoarthritis
nociception
mechanosensing
osmosensing
inflammation
calcium
url http://www.ecmjournal.org/papers/vol034/pdf/v034a12.pdf
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