Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes

The metabolic activity of articular chondrocytes is influenced by osmotic alterations that occur in articular cartilage secondary to mechanical load. The mechanisms that sense and transduce mechanical signals from cell swelling and initiate volume regulation are poorly understood. The purpose of thi...

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Main Authors: Hdud, Ismail M., Mobasheri, Ali, Loughna, Paul
Format: Article
Language:English
Published: American Physiological Society 2014
Subjects:
Online Access:https://eprints.nottingham.ac.uk/46619/
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author Hdud, Ismail M.
Mobasheri, Ali
Loughna, Paul
author_facet Hdud, Ismail M.
Mobasheri, Ali
Loughna, Paul
author_sort Hdud, Ismail M.
building Nottingham Research Data Repository
collection Online Access
description The metabolic activity of articular chondrocytes is influenced by osmotic alterations that occur in articular cartilage secondary to mechanical load. The mechanisms that sense and transduce mechanical signals from cell swelling and initiate volume regulation are poorly understood. The purpose of this study was to investigate how the expression of two putative osmolyte channels [transient receptor potential vanilloid 4 (TRPV4) and large-conductance Ca2+-activated K+ (BKCa)] in chondrocytes is modulated in different osmotic conditions and to examine a potential role for MAPKs in this process. Isolated equine articular chondrocytes were subjected to anisosmotic conditions, and TRPV4 and BKCa channel expression and ERK1/2 and p38 MAPK protein phosphorylation were investigated using Western blotting. Results indicate that the TRPV4 channel contributes to the early stages of hypo-osmotic stress, while the BKCa channel is involved in responding to elevated intracellular Ca2+ and mediating regulatory volume decrease. ERK1/2 is phosphorylated by hypo-osmotic stress (P < 0.001), and p38 MAPK is phosphorylated by hyperosmotic stress (P < 0.001). In addition, this study demonstrates the importance of endogenous ERK1/2 phosphorylation in TRPV4 channel expression, where blocking ERK1/2 by a specific inhibitor (PD98059) prevented increased levels of the TRPV4 channel in cells exposed to hypo-osmotic stress and decreased TRPV4 channel expression to below control levels in iso-osmotic conditions (P < 0.001).
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spelling nottingham-466192020-05-08T12:00:40Z https://eprints.nottingham.ac.uk/46619/ Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes Hdud, Ismail M. Mobasheri, Ali Loughna, Paul The metabolic activity of articular chondrocytes is influenced by osmotic alterations that occur in articular cartilage secondary to mechanical load. The mechanisms that sense and transduce mechanical signals from cell swelling and initiate volume regulation are poorly understood. The purpose of this study was to investigate how the expression of two putative osmolyte channels [transient receptor potential vanilloid 4 (TRPV4) and large-conductance Ca2+-activated K+ (BKCa)] in chondrocytes is modulated in different osmotic conditions and to examine a potential role for MAPKs in this process. Isolated equine articular chondrocytes were subjected to anisosmotic conditions, and TRPV4 and BKCa channel expression and ERK1/2 and p38 MAPK protein phosphorylation were investigated using Western blotting. Results indicate that the TRPV4 channel contributes to the early stages of hypo-osmotic stress, while the BKCa channel is involved in responding to elevated intracellular Ca2+ and mediating regulatory volume decrease. ERK1/2 is phosphorylated by hypo-osmotic stress (P < 0.001), and p38 MAPK is phosphorylated by hyperosmotic stress (P < 0.001). In addition, this study demonstrates the importance of endogenous ERK1/2 phosphorylation in TRPV4 channel expression, where blocking ERK1/2 by a specific inhibitor (PD98059) prevented increased levels of the TRPV4 channel in cells exposed to hypo-osmotic stress and decreased TRPV4 channel expression to below control levels in iso-osmotic conditions (P < 0.001). American Physiological Society 2014-03-26 Article PeerReviewed application/pdf en https://eprints.nottingham.ac.uk/46619/1/C1050.full.pdf Hdud, Ismail M., Mobasheri, Ali and Loughna, Paul (2014) Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes. American Journal of Physiology - Cell Physiology, 306 (11). pp. 1050-1057. ISSN 1522-1563 cartilage; chondrocyte; mitogen-activated protein kinase; osmotic; transient receptor potential vanilloid 4 http://ajpcell.physiology.org/content/306/11/C1050 doi:10.1152/ajpcell.00287.2013 doi:10.1152/ajpcell.00287.2013
spellingShingle cartilage; chondrocyte; mitogen-activated protein kinase; osmotic; transient receptor potential vanilloid 4
Hdud, Ismail M.
Mobasheri, Ali
Loughna, Paul
Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes
title Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes
title_full Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes
title_fullStr Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes
title_full_unstemmed Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes
title_short Effect of osmotic stress on the expression of TRPV4 and BKCa channels and possible interaction with ERK1/2 and p38 in cultured equine chondrocytes
title_sort effect of osmotic stress on the expression of trpv4 and bkca channels and possible interaction with erk1/2 and p38 in cultured equine chondrocytes
topic cartilage; chondrocyte; mitogen-activated protein kinase; osmotic; transient receptor potential vanilloid 4
url https://eprints.nottingham.ac.uk/46619/
https://eprints.nottingham.ac.uk/46619/
https://eprints.nottingham.ac.uk/46619/