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The outer limiting membrane (OLM) revisited: clinical implications
PURPOSE: The outer limiting membrane (OLM) is considered to play a role in maintaining the structure of the retina through mechanical strength. However, the observation of junction proteins located at the OLM and its barrier permeability properties may suggest that the OLM may be part of the retinal...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861922/ https://www.ncbi.nlm.nih.gov/pubmed/20463783 |
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author | Omri, S Omri, B Savoldelli, M Jonet, L Thillaye-Goldenberg, B Thuret, G Gain, P Jeanny, J C Crisanti, P Behar-Cohen, Francine |
author_facet | Omri, S Omri, B Savoldelli, M Jonet, L Thillaye-Goldenberg, B Thuret, G Gain, P Jeanny, J C Crisanti, P Behar-Cohen, Francine |
author_sort | Omri, S |
collection | PubMed |
description | PURPOSE: The outer limiting membrane (OLM) is considered to play a role in maintaining the structure of the retina through mechanical strength. However, the observation of junction proteins located at the OLM and its barrier permeability properties may suggest that the OLM may be part of the retinal barrier. MATERIAL AND METHODS: Normal and diabetic rat, monkey, and human retinas were used to analyze junction proteins at the OLM. Proteome analyses were performed using immunohistochemistry on sections and flat-mounted retinas and western blotting on protein extracts obtained from laser microdissection of the photoreceptor layers. Semi-thin and ultrastructure analyses were also reported. RESULTS: In the rat retina, in the subapical region zonula occludens-1 (ZO-1), junction adhesion molecule (JAM), an atypical protein kinase C, is present and the OLM shows dense labeling of occludin, JAM, and ZO-1. The presence of occludin has been confirmed using western blot analysis of the microdissected OLM region. In diabetic rats, occludin expression is decreased and glial cells junctions are dissociated. In the monkey retina, occludin, JAM, and ZO-1 are also found in the OLM. Junction proteins have a specific distribution around cone photoreceptors and Müller glia. Ultrastructural analyses suggest that structures like tight junctions may exist between retinal glial Müller cells and photoreceptors. CONCLUSIONS: In the OLM, heterotypic junctions contain proteins from both adherent and tight junctions. Their structure suggests that tight junctions may exist in the OLM. Occludin is present in the OLM of the rat and monkey retina and it is decreased in diabetes. The OLM should be considered as part of the retinal barrier that can be disrupted in pathological conditions contributing to fluid accumulation in the macula. |
format | Text |
id | pubmed-2861922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28619222010-05-12 The outer limiting membrane (OLM) revisited: clinical implications Omri, S Omri, B Savoldelli, M Jonet, L Thillaye-Goldenberg, B Thuret, G Gain, P Jeanny, J C Crisanti, P Behar-Cohen, Francine Clin Ophthalmol Original Research PURPOSE: The outer limiting membrane (OLM) is considered to play a role in maintaining the structure of the retina through mechanical strength. However, the observation of junction proteins located at the OLM and its barrier permeability properties may suggest that the OLM may be part of the retinal barrier. MATERIAL AND METHODS: Normal and diabetic rat, monkey, and human retinas were used to analyze junction proteins at the OLM. Proteome analyses were performed using immunohistochemistry on sections and flat-mounted retinas and western blotting on protein extracts obtained from laser microdissection of the photoreceptor layers. Semi-thin and ultrastructure analyses were also reported. RESULTS: In the rat retina, in the subapical region zonula occludens-1 (ZO-1), junction adhesion molecule (JAM), an atypical protein kinase C, is present and the OLM shows dense labeling of occludin, JAM, and ZO-1. The presence of occludin has been confirmed using western blot analysis of the microdissected OLM region. In diabetic rats, occludin expression is decreased and glial cells junctions are dissociated. In the monkey retina, occludin, JAM, and ZO-1 are also found in the OLM. Junction proteins have a specific distribution around cone photoreceptors and Müller glia. Ultrastructural analyses suggest that structures like tight junctions may exist between retinal glial Müller cells and photoreceptors. CONCLUSIONS: In the OLM, heterotypic junctions contain proteins from both adherent and tight junctions. Their structure suggests that tight junctions may exist in the OLM. Occludin is present in the OLM of the rat and monkey retina and it is decreased in diabetes. The OLM should be considered as part of the retinal barrier that can be disrupted in pathological conditions contributing to fluid accumulation in the macula. Dove Medical Press 2010 2010-04-26 /pmc/articles/PMC2861922/ /pubmed/20463783 Text en © 2010 Omri et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Omri, S Omri, B Savoldelli, M Jonet, L Thillaye-Goldenberg, B Thuret, G Gain, P Jeanny, J C Crisanti, P Behar-Cohen, Francine The outer limiting membrane (OLM) revisited: clinical implications |
title | The outer limiting membrane (OLM) revisited: clinical implications |
title_full | The outer limiting membrane (OLM) revisited: clinical implications |
title_fullStr | The outer limiting membrane (OLM) revisited: clinical implications |
title_full_unstemmed | The outer limiting membrane (OLM) revisited: clinical implications |
title_short | The outer limiting membrane (OLM) revisited: clinical implications |
title_sort | outer limiting membrane (olm) revisited: clinical implications |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861922/ https://www.ncbi.nlm.nih.gov/pubmed/20463783 |
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