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Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium
The retinal pigment epithelium located between the neurosensory retina and the choroidal vasculature is critical for the function and maintenance of both the photoreceptors and underlying capillary endothelium. While the trophic role of retinal pigment epithelium on choroidal endothelial cells is we...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618686/ https://www.ncbi.nlm.nih.gov/pubmed/28402065 http://dx.doi.org/10.1111/jcmm.13175 |
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author | Spencer, Carrie Abend, Stephanie McHugh, Kevin J. Saint‐Geniez, Magali |
author_facet | Spencer, Carrie Abend, Stephanie McHugh, Kevin J. Saint‐Geniez, Magali |
author_sort | Spencer, Carrie |
collection | PubMed |
description | The retinal pigment epithelium located between the neurosensory retina and the choroidal vasculature is critical for the function and maintenance of both the photoreceptors and underlying capillary endothelium. While the trophic role of retinal pigment epithelium on choroidal endothelial cells is well recognized, the existence of a reciprocal regulatory function of endothelial cells on retinal pigment epithelium cells remained to be fully characterized. Using a physiological long‐term co‐culture system, we determined the effect of retinal pigment epithelium‐endothelial cell heterotypic interactions on cell survival, behaviour and matrix deposition. Human retinal pigment epithelium and endothelial cells were cultured on opposite sides of polyester transwells for up to 4 weeks in low serum conditions. Cell viability was quantified using a trypan blue assay. Cellular morphology was evaluated by H&E staining, S.E.M. and immunohistochemistry. Retinal pigment epithelium phagocytic function was examined using a fluorescent bead assay. Gene expression analysis was performed on both retinal pigment epithelium and endothelial cells by quantitative PCR. Quantification of extracellular matrix deposition was performed on decellularized transwells stained for collagen IV, fibronectin and fibrillin. Our results showed that presence of endothelial cells significantly improves retinal pigment epithelium maturation and function as indicated by the induction of visual cycle‐associated genes, accumulation of a Bruch's membrane‐like matrix and increase in retinal pigment epithelium phagocytic activity. Co‐culture conditions led to increased expression of anti‐angiogenic growth factors and receptors in both retinal pigment epithelium and endothelial cells compared to monoculture. Tube‐formation assays confirmed that co‐culture with retinal pigment epithelium significantly decreased the angiogenic phenotype of endothelial cells. These findings provide evidence of critical interdependent interactions between retinal pigment epithelium and endothelial cell involved in the maintenance of retinal homeostasis. |
format | Online Article Text |
id | pubmed-5618686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56186862017-10-04 Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium Spencer, Carrie Abend, Stephanie McHugh, Kevin J. Saint‐Geniez, Magali J Cell Mol Med Original Articles The retinal pigment epithelium located between the neurosensory retina and the choroidal vasculature is critical for the function and maintenance of both the photoreceptors and underlying capillary endothelium. While the trophic role of retinal pigment epithelium on choroidal endothelial cells is well recognized, the existence of a reciprocal regulatory function of endothelial cells on retinal pigment epithelium cells remained to be fully characterized. Using a physiological long‐term co‐culture system, we determined the effect of retinal pigment epithelium‐endothelial cell heterotypic interactions on cell survival, behaviour and matrix deposition. Human retinal pigment epithelium and endothelial cells were cultured on opposite sides of polyester transwells for up to 4 weeks in low serum conditions. Cell viability was quantified using a trypan blue assay. Cellular morphology was evaluated by H&E staining, S.E.M. and immunohistochemistry. Retinal pigment epithelium phagocytic function was examined using a fluorescent bead assay. Gene expression analysis was performed on both retinal pigment epithelium and endothelial cells by quantitative PCR. Quantification of extracellular matrix deposition was performed on decellularized transwells stained for collagen IV, fibronectin and fibrillin. Our results showed that presence of endothelial cells significantly improves retinal pigment epithelium maturation and function as indicated by the induction of visual cycle‐associated genes, accumulation of a Bruch's membrane‐like matrix and increase in retinal pigment epithelium phagocytic activity. Co‐culture conditions led to increased expression of anti‐angiogenic growth factors and receptors in both retinal pigment epithelium and endothelial cells compared to monoculture. Tube‐formation assays confirmed that co‐culture with retinal pigment epithelium significantly decreased the angiogenic phenotype of endothelial cells. These findings provide evidence of critical interdependent interactions between retinal pigment epithelium and endothelial cell involved in the maintenance of retinal homeostasis. John Wiley and Sons Inc. 2017-04-12 2017-10 /pmc/articles/PMC5618686/ /pubmed/28402065 http://dx.doi.org/10.1111/jcmm.13175 Text en © 2017 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Spencer, Carrie Abend, Stephanie McHugh, Kevin J. Saint‐Geniez, Magali Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
title | Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
title_full | Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
title_fullStr | Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
title_full_unstemmed | Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
title_short | Identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
title_sort | identification of a synergistic interaction between endothelial cells and retinal pigment epithelium |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618686/ https://www.ncbi.nlm.nih.gov/pubmed/28402065 http://dx.doi.org/10.1111/jcmm.13175 |
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