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Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation
PURPOSE: For an aqueous shunt draining from the anterior chamber into the choroidal space, fibroblasts from the choroidea and/or the sclera are most likely responsible for a fibrotic response around the outflow region of such a shunt. The prevention of fibrosis should extend the operating life of th...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692408/ https://www.ncbi.nlm.nih.gov/pubmed/23805039 |
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author | Löbler, Marian Buß, Diana Kastner, Christian Mostertz, Jörg Homuth, Georg Ernst, Mathias Guthoff, Rudolf Wree, Andreas Stahnke, Thomas Fuellen, Georg Voelker, Uwe Schmitz, Klaus-Peter |
author_facet | Löbler, Marian Buß, Diana Kastner, Christian Mostertz, Jörg Homuth, Georg Ernst, Mathias Guthoff, Rudolf Wree, Andreas Stahnke, Thomas Fuellen, Georg Voelker, Uwe Schmitz, Klaus-Peter |
author_sort | Löbler, Marian |
collection | PubMed |
description | PURPOSE: For an aqueous shunt draining from the anterior chamber into the choroidal space, fibroblasts from the choroidea and/or the sclera are most likely responsible for a fibrotic response around the outflow region of such a shunt. The prevention of fibrosis should extend the operating life of the shunt. A detailed characterization of fibroblasts derived from choroidea and sclera should provide information about whether a fibrosis reaction can be inhibited by cell type-specific agents. METHODS: We generated mRNA profiles of fibroblasts from the choroidea, sclera, and Tenon’s space by gene array hybridization to provide a basis on which to search for potential pharmacological targets for fibrosis prevention. Hybridization data were analyzed by the Rosetta Resolver system and Limma to obtain mRNA profiles of the three fibroblast types. RESULTS: The three fibroblast types investigated shared fibroblast-specific gene expression patterns concerning extracellular matrix proteins as collagens and fibronectin, but also showed distinct mRNA patterns. CONCLUSIONS: Individual mRNA species overexpressed in one of the fibroblast types might serve as markers for the identification of the fibroblast type in histological analyses. Future in-depth analyses of the gene expression patterns might help identify pharmacological targets for fibrosis prevention. |
format | Online Article Text |
id | pubmed-3692408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-36924082013-06-26 Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation Löbler, Marian Buß, Diana Kastner, Christian Mostertz, Jörg Homuth, Georg Ernst, Mathias Guthoff, Rudolf Wree, Andreas Stahnke, Thomas Fuellen, Georg Voelker, Uwe Schmitz, Klaus-Peter Mol Vis Research Article PURPOSE: For an aqueous shunt draining from the anterior chamber into the choroidal space, fibroblasts from the choroidea and/or the sclera are most likely responsible for a fibrotic response around the outflow region of such a shunt. The prevention of fibrosis should extend the operating life of the shunt. A detailed characterization of fibroblasts derived from choroidea and sclera should provide information about whether a fibrosis reaction can be inhibited by cell type-specific agents. METHODS: We generated mRNA profiles of fibroblasts from the choroidea, sclera, and Tenon’s space by gene array hybridization to provide a basis on which to search for potential pharmacological targets for fibrosis prevention. Hybridization data were analyzed by the Rosetta Resolver system and Limma to obtain mRNA profiles of the three fibroblast types. RESULTS: The three fibroblast types investigated shared fibroblast-specific gene expression patterns concerning extracellular matrix proteins as collagens and fibronectin, but also showed distinct mRNA patterns. CONCLUSIONS: Individual mRNA species overexpressed in one of the fibroblast types might serve as markers for the identification of the fibroblast type in histological analyses. Future in-depth analyses of the gene expression patterns might help identify pharmacological targets for fibrosis prevention. Molecular Vision 2013-06-12 /pmc/articles/PMC3692408/ /pubmed/23805039 Text en Copyright © 2013 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Löbler, Marian Buß, Diana Kastner, Christian Mostertz, Jörg Homuth, Georg Ernst, Mathias Guthoff, Rudolf Wree, Andreas Stahnke, Thomas Fuellen, Georg Voelker, Uwe Schmitz, Klaus-Peter Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation |
title | Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation |
title_full | Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation |
title_fullStr | Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation |
title_full_unstemmed | Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation |
title_short | Ocular fibroblast types differ in their mRNA profiles—implications for fibrosis prevention after aqueous shunt implantation |
title_sort | ocular fibroblast types differ in their mrna profiles—implications for fibrosis prevention after aqueous shunt implantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3692408/ https://www.ncbi.nlm.nih.gov/pubmed/23805039 |
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