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Characterization of extracellular matrix deposited by segmental trabecular meshwork cells
Biophysical and biochemical attributes of the extracellular matrix are major determinants of cell fate in homeostasis and disease. Ocular hypertension and glaucoma are diseases where the trabecular meshwork tissue responsible for aqueous humor egress becomes stiffer accompanied by changes in its mat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028995/ https://www.ncbi.nlm.nih.gov/pubmed/36945588 http://dx.doi.org/10.1101/2023.03.11.532242 |
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author | Raghunathan, VijayKrishna Nartey, Andrews Dhamodaran, Kamesh Baidouri, Hasna Staverosky, Julia A. Keller, Kate E Zientek, Keith Reddy, Ashok Acott, Ted Vranka, Janice A |
author_facet | Raghunathan, VijayKrishna Nartey, Andrews Dhamodaran, Kamesh Baidouri, Hasna Staverosky, Julia A. Keller, Kate E Zientek, Keith Reddy, Ashok Acott, Ted Vranka, Janice A |
author_sort | Raghunathan, VijayKrishna |
collection | PubMed |
description | Biophysical and biochemical attributes of the extracellular matrix are major determinants of cell fate in homeostasis and disease. Ocular hypertension and glaucoma are diseases where the trabecular meshwork tissue responsible for aqueous humor egress becomes stiffer accompanied by changes in its matrisome in a segmental manner with regions of high or low flow. Prior studies demonstrate these alterations in the matrix are dynamic in response to age and pressure changes. The underlying reason for segmentation or differential response to pressure and stiffening are unknown. This is largely due to a lack of appropriate models (in vitro or ex vivo) to study this phenomena. In this study, we characterize the biomechanical attributes, matrisome, and incidence of crosslinks in the matrix deposited by primary cells isolated from segmental flow regions and when treated with glucocorticosteroid. Data demonstrate that matrix deposited by cells from low flow regions are stiffer and exhibit a greater number of immature and mature crosslinks, and that these are exacerbated in the presence of steroid. We also show a differential response of high or low flow cells to steroid via changes observed in the matrix composition. We conclude that although a mechanistic basis for matrix stiffness was undetermined in this study, it is a viable tool to study cell-matrix interactions and further our understanding of trabecular meshwork pathobiology. |
format | Online Article Text |
id | pubmed-10028995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100289952023-03-22 Characterization of extracellular matrix deposited by segmental trabecular meshwork cells Raghunathan, VijayKrishna Nartey, Andrews Dhamodaran, Kamesh Baidouri, Hasna Staverosky, Julia A. Keller, Kate E Zientek, Keith Reddy, Ashok Acott, Ted Vranka, Janice A bioRxiv Article Biophysical and biochemical attributes of the extracellular matrix are major determinants of cell fate in homeostasis and disease. Ocular hypertension and glaucoma are diseases where the trabecular meshwork tissue responsible for aqueous humor egress becomes stiffer accompanied by changes in its matrisome in a segmental manner with regions of high or low flow. Prior studies demonstrate these alterations in the matrix are dynamic in response to age and pressure changes. The underlying reason for segmentation or differential response to pressure and stiffening are unknown. This is largely due to a lack of appropriate models (in vitro or ex vivo) to study this phenomena. In this study, we characterize the biomechanical attributes, matrisome, and incidence of crosslinks in the matrix deposited by primary cells isolated from segmental flow regions and when treated with glucocorticosteroid. Data demonstrate that matrix deposited by cells from low flow regions are stiffer and exhibit a greater number of immature and mature crosslinks, and that these are exacerbated in the presence of steroid. We also show a differential response of high or low flow cells to steroid via changes observed in the matrix composition. We conclude that although a mechanistic basis for matrix stiffness was undetermined in this study, it is a viable tool to study cell-matrix interactions and further our understanding of trabecular meshwork pathobiology. Cold Spring Harbor Laboratory 2023-03-12 /pmc/articles/PMC10028995/ /pubmed/36945588 http://dx.doi.org/10.1101/2023.03.11.532242 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Raghunathan, VijayKrishna Nartey, Andrews Dhamodaran, Kamesh Baidouri, Hasna Staverosky, Julia A. Keller, Kate E Zientek, Keith Reddy, Ashok Acott, Ted Vranka, Janice A Characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
title | Characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
title_full | Characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
title_fullStr | Characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
title_full_unstemmed | Characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
title_short | Characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
title_sort | characterization of extracellular matrix deposited by segmental trabecular meshwork cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028995/ https://www.ncbi.nlm.nih.gov/pubmed/36945588 http://dx.doi.org/10.1101/2023.03.11.532242 |
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