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Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea

PURPOSE: We sought to identify the anti-angiogenic molecule expressed in corneal keratocytes that is responsible for maintaining the avascularity of the cornea. METHODS: Human umbilical vein endothelial cells (HUVECs) were cultured with either human dermal fibroblasts or with human corneal keratocyt...

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Autores principales: Toyono, Tetsuya, Usui, Tomohiko, Yokoo, Seiichi, Taketani, Yukako, Nakagawa, Suguru, Kuroda, Masahiko, Yamagami, Satoru, Amano, Shiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306551/
https://www.ncbi.nlm.nih.gov/pubmed/25622036
http://dx.doi.org/10.1371/journal.pone.0116838
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author Toyono, Tetsuya
Usui, Tomohiko
Yokoo, Seiichi
Taketani, Yukako
Nakagawa, Suguru
Kuroda, Masahiko
Yamagami, Satoru
Amano, Shiro
author_facet Toyono, Tetsuya
Usui, Tomohiko
Yokoo, Seiichi
Taketani, Yukako
Nakagawa, Suguru
Kuroda, Masahiko
Yamagami, Satoru
Amano, Shiro
author_sort Toyono, Tetsuya
collection PubMed
description PURPOSE: We sought to identify the anti-angiogenic molecule expressed in corneal keratocytes that is responsible for maintaining the avascularity of the cornea. METHODS: Human umbilical vein endothelial cells (HUVECs) were cultured with either human dermal fibroblasts or with human corneal keratocytes under serum-free conditions. The areas that exhibited blood vessel formation were estimated by immunostaining the cultures with an antitibody against CD31, a blood vessel marker. We also performed microarray gene-expression analysis and selected one molecule, angiopoietin-like 7 (ANGPTL7) for further functional studies conducted with the keratocytes and in vivo in mice. RESULTS: Areas showing blood vessel formation in normal serum-free medium were conditions were markedly smaller when HUVECs were co-cultured with corneal keratocytes than when they were co-cultured with the dermal fibroblasts under the same conditions. Microarray analysis revealed that ANGPTL7 expression was higher in keratocytes than in dermal fibroblasts. In vitro, inhibiting ANGPTL7 expression by using a specific siRNA led to greater tube formation than did the transfection of cells with a control siRNA, and this increase in tube formation was abolished when recombinant ANGPTL7 protein was added to the cultures. In vivo, intrastromal injections of an ANGPTL7 PshRNA into the avascular corneal stroma of mice resulted in the growth of blood vessels. CONCLUSIONS: ANGPTL7, which is abundantly expressed in keratocytes, plays a major role in maintaining corneal avascularity and transparency.
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spelling pubmed-43065512015-01-30 Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea Toyono, Tetsuya Usui, Tomohiko Yokoo, Seiichi Taketani, Yukako Nakagawa, Suguru Kuroda, Masahiko Yamagami, Satoru Amano, Shiro PLoS One Research Article PURPOSE: We sought to identify the anti-angiogenic molecule expressed in corneal keratocytes that is responsible for maintaining the avascularity of the cornea. METHODS: Human umbilical vein endothelial cells (HUVECs) were cultured with either human dermal fibroblasts or with human corneal keratocytes under serum-free conditions. The areas that exhibited blood vessel formation were estimated by immunostaining the cultures with an antitibody against CD31, a blood vessel marker. We also performed microarray gene-expression analysis and selected one molecule, angiopoietin-like 7 (ANGPTL7) for further functional studies conducted with the keratocytes and in vivo in mice. RESULTS: Areas showing blood vessel formation in normal serum-free medium were conditions were markedly smaller when HUVECs were co-cultured with corneal keratocytes than when they were co-cultured with the dermal fibroblasts under the same conditions. Microarray analysis revealed that ANGPTL7 expression was higher in keratocytes than in dermal fibroblasts. In vitro, inhibiting ANGPTL7 expression by using a specific siRNA led to greater tube formation than did the transfection of cells with a control siRNA, and this increase in tube formation was abolished when recombinant ANGPTL7 protein was added to the cultures. In vivo, intrastromal injections of an ANGPTL7 PshRNA into the avascular corneal stroma of mice resulted in the growth of blood vessels. CONCLUSIONS: ANGPTL7, which is abundantly expressed in keratocytes, plays a major role in maintaining corneal avascularity and transparency. Public Library of Science 2015-01-26 /pmc/articles/PMC4306551/ /pubmed/25622036 http://dx.doi.org/10.1371/journal.pone.0116838 Text en © 2015 Toyono et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Toyono, Tetsuya
Usui, Tomohiko
Yokoo, Seiichi
Taketani, Yukako
Nakagawa, Suguru
Kuroda, Masahiko
Yamagami, Satoru
Amano, Shiro
Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea
title Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea
title_full Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea
title_fullStr Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea
title_full_unstemmed Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea
title_short Angiopoietin-Like 7 Is an Anti-Angiogenic Protein Required to Prevent Vascularization of the Cornea
title_sort angiopoietin-like 7 is an anti-angiogenic protein required to prevent vascularization of the cornea
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306551/
https://www.ncbi.nlm.nih.gov/pubmed/25622036
http://dx.doi.org/10.1371/journal.pone.0116838
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