Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure

Abstract In the eye, intraocular pressure (IOP) is tightly regulated and its persistent increase leads to ocular hypertension and glaucoma. We have previously shown that trabecular meshwork (TM) cells might detect aqueous humor fluid shear stress via interaction of the extracellular matrix (ECM) pro...

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Main Authors: Teresia A. Carreon, Aida Castellanos, Xavier Gasull, Sanjoy K. Bhattacharya
Format: Article
Language:English
Published: Nature Publishing Group 2017-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-00430-2
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spelling doaj-0f9f8ab4fd0649ebb60fa5214f2cdc002020-12-08T00:08:22ZengNature Publishing GroupScientific Reports2045-23222017-03-017111110.1038/s41598-017-00430-2Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressureTeresia A. Carreon0Aida Castellanos1Xavier Gasull2Sanjoy K. Bhattacharya3Bascom Palmer Eye Institute, University of MiamiDepartment of Biomedicine, University of BarcelonaDepartment of Biomedicine, University of BarcelonaBascom Palmer Eye Institute, University of MiamiAbstract In the eye, intraocular pressure (IOP) is tightly regulated and its persistent increase leads to ocular hypertension and glaucoma. We have previously shown that trabecular meshwork (TM) cells might detect aqueous humor fluid shear stress via interaction of the extracellular matrix (ECM) protein cochlin with the cell surface bound and stretch-activated channel TREK-1. We provide evidence here that interaction between both proteins are involved in IOP regulation. Silencing of TREK-1 in mice prevents the previously demonstrated cochlin-overexpression mediated increase in IOP. Biochemical and electrophysiological experiments demonstrate that high shear stress-induced multimeric cochlin produces a qualitatively different interaction with TREK-1 compared to monomeric cochlin. Physiological concentrations of multimeric but not monomeric cochlin reduce TREK-1 current. Results presented here indicate that the interaction of TREK-1 and cochlin play an important role for maintaining IOP homeostasis.https://doi.org/10.1038/s41598-017-00430-2
collection DOAJ
language English
format Article
sources DOAJ
author Teresia A. Carreon
Aida Castellanos
Xavier Gasull
Sanjoy K. Bhattacharya
spellingShingle Teresia A. Carreon
Aida Castellanos
Xavier Gasull
Sanjoy K. Bhattacharya
Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure
Scientific Reports
author_facet Teresia A. Carreon
Aida Castellanos
Xavier Gasull
Sanjoy K. Bhattacharya
author_sort Teresia A. Carreon
title Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure
title_short Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure
title_full Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure
title_fullStr Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure
title_full_unstemmed Interaction of cochlin and mechanosensitive channel TREK-1 in trabecular meshwork cells influences the regulation of intraocular pressure
title_sort interaction of cochlin and mechanosensitive channel trek-1 in trabecular meshwork cells influences the regulation of intraocular pressure
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-03-01
description Abstract In the eye, intraocular pressure (IOP) is tightly regulated and its persistent increase leads to ocular hypertension and glaucoma. We have previously shown that trabecular meshwork (TM) cells might detect aqueous humor fluid shear stress via interaction of the extracellular matrix (ECM) protein cochlin with the cell surface bound and stretch-activated channel TREK-1. We provide evidence here that interaction between both proteins are involved in IOP regulation. Silencing of TREK-1 in mice prevents the previously demonstrated cochlin-overexpression mediated increase in IOP. Biochemical and electrophysiological experiments demonstrate that high shear stress-induced multimeric cochlin produces a qualitatively different interaction with TREK-1 compared to monomeric cochlin. Physiological concentrations of multimeric but not monomeric cochlin reduce TREK-1 current. Results presented here indicate that the interaction of TREK-1 and cochlin play an important role for maintaining IOP homeostasis.
url https://doi.org/10.1038/s41598-017-00430-2
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