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The relationship between outflow resistance and trabecular meshwork stiffness in mice

It has been suggested that common mechanisms may underlie the pathogenesis of primary open-angle glaucoma (POAG) and steroid-induced glaucoma (SIG). The biomechanical properties (stiffness) of the trabecular meshwork (TM) have been shown to differ between POAG patients and unaffected individuals. Wh...

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Autores principales: Wang, Ke, Li, Guorong, Read, A. Thomas, Navarro, Iris, Mitra, Ashim K., Stamer, W. Daniel, Sulchek, Todd, Ethier, C. Ross
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895808/
https://www.ncbi.nlm.nih.gov/pubmed/29643342
http://dx.doi.org/10.1038/s41598-018-24165-w
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author Wang, Ke
Li, Guorong
Read, A. Thomas
Navarro, Iris
Mitra, Ashim K.
Stamer, W. Daniel
Sulchek, Todd
Ethier, C. Ross
author_facet Wang, Ke
Li, Guorong
Read, A. Thomas
Navarro, Iris
Mitra, Ashim K.
Stamer, W. Daniel
Sulchek, Todd
Ethier, C. Ross
author_sort Wang, Ke
collection PubMed
description It has been suggested that common mechanisms may underlie the pathogenesis of primary open-angle glaucoma (POAG) and steroid-induced glaucoma (SIG). The biomechanical properties (stiffness) of the trabecular meshwork (TM) have been shown to differ between POAG patients and unaffected individuals. While features such as ocular hypertension and increased outflow resistance in POAG and SIG have been replicated in mouse models, whether changes of TM stiffness contributes to altered IOP homeostasis remains unknown. We found that outer TM was stiffer than the inner TM and, there was a significant positive correlation between outflow resistance and TM stiffness in mice where conditions are well controlled. This suggests that TM stiffness is intimately involved in establishing outflow resistance, motivating further studies to investigate factors underlying TM biomechanical property regulation. Such factors may play a role in the pathophysiology of ocular hypertension. Additionally, this finding may imply that manipulating TM may be a promising approach to restore normal outflow dynamics in glaucoma. Further, novel technologies are being developed to measure ocular tissue stiffness in situ. Thus, the changes of TM stiffness might be a surrogate marker to help in diagnosing altered conventional outflow pathway function if those technologies could be adapted to TM.
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spelling pubmed-58958082018-04-20 The relationship between outflow resistance and trabecular meshwork stiffness in mice Wang, Ke Li, Guorong Read, A. Thomas Navarro, Iris Mitra, Ashim K. Stamer, W. Daniel Sulchek, Todd Ethier, C. Ross Sci Rep Article It has been suggested that common mechanisms may underlie the pathogenesis of primary open-angle glaucoma (POAG) and steroid-induced glaucoma (SIG). The biomechanical properties (stiffness) of the trabecular meshwork (TM) have been shown to differ between POAG patients and unaffected individuals. While features such as ocular hypertension and increased outflow resistance in POAG and SIG have been replicated in mouse models, whether changes of TM stiffness contributes to altered IOP homeostasis remains unknown. We found that outer TM was stiffer than the inner TM and, there was a significant positive correlation between outflow resistance and TM stiffness in mice where conditions are well controlled. This suggests that TM stiffness is intimately involved in establishing outflow resistance, motivating further studies to investigate factors underlying TM biomechanical property regulation. Such factors may play a role in the pathophysiology of ocular hypertension. Additionally, this finding may imply that manipulating TM may be a promising approach to restore normal outflow dynamics in glaucoma. Further, novel technologies are being developed to measure ocular tissue stiffness in situ. Thus, the changes of TM stiffness might be a surrogate marker to help in diagnosing altered conventional outflow pathway function if those technologies could be adapted to TM. Nature Publishing Group UK 2018-04-11 /pmc/articles/PMC5895808/ /pubmed/29643342 http://dx.doi.org/10.1038/s41598-018-24165-w Text en © The Author(s) 2018 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
Wang, Ke
Li, Guorong
Read, A. Thomas
Navarro, Iris
Mitra, Ashim K.
Stamer, W. Daniel
Sulchek, Todd
Ethier, C. Ross
The relationship between outflow resistance and trabecular meshwork stiffness in mice
title The relationship between outflow resistance and trabecular meshwork stiffness in mice
title_full The relationship between outflow resistance and trabecular meshwork stiffness in mice
title_fullStr The relationship between outflow resistance and trabecular meshwork stiffness in mice
title_full_unstemmed The relationship between outflow resistance and trabecular meshwork stiffness in mice
title_short The relationship between outflow resistance and trabecular meshwork stiffness in mice
title_sort relationship between outflow resistance and trabecular meshwork stiffness in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895808/
https://www.ncbi.nlm.nih.gov/pubmed/29643342
http://dx.doi.org/10.1038/s41598-018-24165-w
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