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Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors
The outer blood-retina barrier is established through the coordinated terminal maturation of the retinal pigment epithelium (RPE), fenestrated choroid endothelial cells (ECs) and Bruch's membrane, a highly organized basement membrane that lies between both cell types. Here we study the contribu...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454459/ https://www.ncbi.nlm.nih.gov/pubmed/28524846 http://dx.doi.org/10.1038/ncomms15374 |
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author | Benedicto, Ignacio Lehmann, Guillermo L. Ginsberg, Michael Nolan, Daniel J. Bareja, Rohan Elemento, Olivier Salfati, Zelda Alam, Nazia M. Prusky, Glen T. Llanos, Pierre Rabbany, Sina Y. Maminishkis, Arvydas Miller, Sheldon S. Rafii, Shahin Rodriguez-Boulan, Enrique |
author_facet | Benedicto, Ignacio Lehmann, Guillermo L. Ginsberg, Michael Nolan, Daniel J. Bareja, Rohan Elemento, Olivier Salfati, Zelda Alam, Nazia M. Prusky, Glen T. Llanos, Pierre Rabbany, Sina Y. Maminishkis, Arvydas Miller, Sheldon S. Rafii, Shahin Rodriguez-Boulan, Enrique |
author_sort | Benedicto, Ignacio |
collection | PubMed |
description | The outer blood-retina barrier is established through the coordinated terminal maturation of the retinal pigment epithelium (RPE), fenestrated choroid endothelial cells (ECs) and Bruch's membrane, a highly organized basement membrane that lies between both cell types. Here we study the contribution of choroid ECs to this process by comparing their gene expression profile before (P5) and after (P30) the critical postnatal period when mice acquire mature visual function. Transcriptome analyses show that expression of extracellular matrix-related genes changes dramatically over this period. Co-culture experiments support the existence of a novel regulatory pathway: ECs secrete factors that remodel RPE basement membrane, and integrin receptors sense these changes triggering Rho GTPase signals that modulate RPE tight junctions and enhance RPE barrier function. We anticipate our results will spawn a search for additional roles of choroid ECs in RPE physiology and disease. |
format | Online Article Text |
id | pubmed-5454459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54544592017-06-07 Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors Benedicto, Ignacio Lehmann, Guillermo L. Ginsberg, Michael Nolan, Daniel J. Bareja, Rohan Elemento, Olivier Salfati, Zelda Alam, Nazia M. Prusky, Glen T. Llanos, Pierre Rabbany, Sina Y. Maminishkis, Arvydas Miller, Sheldon S. Rafii, Shahin Rodriguez-Boulan, Enrique Nat Commun Article The outer blood-retina barrier is established through the coordinated terminal maturation of the retinal pigment epithelium (RPE), fenestrated choroid endothelial cells (ECs) and Bruch's membrane, a highly organized basement membrane that lies between both cell types. Here we study the contribution of choroid ECs to this process by comparing their gene expression profile before (P5) and after (P30) the critical postnatal period when mice acquire mature visual function. Transcriptome analyses show that expression of extracellular matrix-related genes changes dramatically over this period. Co-culture experiments support the existence of a novel regulatory pathway: ECs secrete factors that remodel RPE basement membrane, and integrin receptors sense these changes triggering Rho GTPase signals that modulate RPE tight junctions and enhance RPE barrier function. We anticipate our results will spawn a search for additional roles of choroid ECs in RPE physiology and disease. Nature Publishing Group 2017-05-19 /pmc/articles/PMC5454459/ /pubmed/28524846 http://dx.doi.org/10.1038/ncomms15374 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Benedicto, Ignacio Lehmann, Guillermo L. Ginsberg, Michael Nolan, Daniel J. Bareja, Rohan Elemento, Olivier Salfati, Zelda Alam, Nazia M. Prusky, Glen T. Llanos, Pierre Rabbany, Sina Y. Maminishkis, Arvydas Miller, Sheldon S. Rafii, Shahin Rodriguez-Boulan, Enrique Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
title | Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
title_full | Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
title_fullStr | Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
title_full_unstemmed | Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
title_short | Concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
title_sort | concerted regulation of retinal pigment epithelium basement membrane and barrier function by angiocrine factors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454459/ https://www.ncbi.nlm.nih.gov/pubmed/28524846 http://dx.doi.org/10.1038/ncomms15374 |
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