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ETX1 is over-expressed in the glaucomatous trabecular meshwork

PURPOSE: To determine whether exon-trapped X chromosome clone 1 (ETX1) is overexpressed in the trabecular meshwork (TM) of glaucomatous human eyes compared to controls. METHODS: Immunohistochemical, western blot, and enzyme-linked immunosorbent assay analysis were used with human tissues and TM prot...

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Autores principales: Iragavarapu, Saradha, Algeciras, Mabel E., Lee, Richard K., Bhattacharya, Sanjoy K.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765241/
https://www.ncbi.nlm.nih.gov/pubmed/19862339
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author Iragavarapu, Saradha
Algeciras, Mabel E.
Lee, Richard K.
Bhattacharya, Sanjoy K.
author_facet Iragavarapu, Saradha
Algeciras, Mabel E.
Lee, Richard K.
Bhattacharya, Sanjoy K.
author_sort Iragavarapu, Saradha
collection PubMed
description PURPOSE: To determine whether exon-trapped X chromosome clone 1 (ETX1) is overexpressed in the trabecular meshwork (TM) of glaucomatous human eyes compared to controls. METHODS: Immunohistochemical, western blot, and enzyme-linked immunosorbent assay analysis were used with human tissues and TM protein extracts. Reverse transcription-PCR was performed on isolated mRNA-derived cDNA preparations. RESULTS: Elevated expression levels of ETX1 were detected in glaucomatous compared to control TM tissue. This corroborates previous detection of ETX1 in glaucomatous TM by proteomic analysis. ETX1 mRNA is present in TM tissue, suggesting ETX1 protein is locally produced within TM cells. CONCLUSIONS: This is the first report demonstrating overexpression of ETX1 in glaucomatous TM. ETX1 expression may regulate TM protein interactions involved in cell adhesion, and its aberrant overexpression may be part of the pathophysiological pathway in the development of glaucoma.
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spelling pubmed-27652412009-10-27 ETX1 is over-expressed in the glaucomatous trabecular meshwork Iragavarapu, Saradha Algeciras, Mabel E. Lee, Richard K. Bhattacharya, Sanjoy K. Mol Vis Research Article PURPOSE: To determine whether exon-trapped X chromosome clone 1 (ETX1) is overexpressed in the trabecular meshwork (TM) of glaucomatous human eyes compared to controls. METHODS: Immunohistochemical, western blot, and enzyme-linked immunosorbent assay analysis were used with human tissues and TM protein extracts. Reverse transcription-PCR was performed on isolated mRNA-derived cDNA preparations. RESULTS: Elevated expression levels of ETX1 were detected in glaucomatous compared to control TM tissue. This corroborates previous detection of ETX1 in glaucomatous TM by proteomic analysis. ETX1 mRNA is present in TM tissue, suggesting ETX1 protein is locally produced within TM cells. CONCLUSIONS: This is the first report demonstrating overexpression of ETX1 in glaucomatous TM. ETX1 expression may regulate TM protein interactions involved in cell adhesion, and its aberrant overexpression may be part of the pathophysiological pathway in the development of glaucoma. Molecular Vision 2009-10-16 /pmc/articles/PMC2765241/ /pubmed/19862339 Text en 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
Iragavarapu, Saradha
Algeciras, Mabel E.
Lee, Richard K.
Bhattacharya, Sanjoy K.
ETX1 is over-expressed in the glaucomatous trabecular meshwork
title ETX1 is over-expressed in the glaucomatous trabecular meshwork
title_full ETX1 is over-expressed in the glaucomatous trabecular meshwork
title_fullStr ETX1 is over-expressed in the glaucomatous trabecular meshwork
title_full_unstemmed ETX1 is over-expressed in the glaucomatous trabecular meshwork
title_short ETX1 is over-expressed in the glaucomatous trabecular meshwork
title_sort etx1 is over-expressed in the glaucomatous trabecular meshwork
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765241/
https://www.ncbi.nlm.nih.gov/pubmed/19862339
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