Expression of classical components of the renin-angiotensin system in the human eye

Purpose: The purpose of this study was to determine the relative expression of clinically-relevant components of the renin-angiotensin system (RAS) in the adult human eye. Methods: We obtained 14 post-mortem enucleated human eyes from patients whom had no history of inflammatory ocular disease nor p...

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Main Authors: Andrew JR White, Sarat C Cheruvu, Maria Sarris, Surabhi S Liyanage, Eugenie Lumbers, Jeanie Chui, Denis Wakefield, Peter J McCluskey
Format: Article
Language:English
Published: Hindawi - SAGE Publishing 2015-03-01
Series:Journal of the Renin-Angiotensin-Aldosterone System
Online Access:https://doi.org/10.1177/1470320314549791
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spelling doaj-dc602b50ddbe4c738964681f28539e9f2021-05-02T14:43:58ZengHindawi - SAGE PublishingJournal of the Renin-Angiotensin-Aldosterone System1470-32031752-89762015-03-011610.1177/1470320314549791Expression of classical components of the renin-angiotensin system in the human eyeAndrew JR White0Sarat C Cheruvu1Maria Sarris2Surabhi S Liyanage3Eugenie Lumbers4Jeanie Chui5Denis Wakefield6Peter J McCluskey7Westmead Millennium Institute, University of Sydney, Sydney, AustraliaSchool of Medical Sciences, University of New South Wales, Sydney, AustraliaDepartment of Physiology, University of New South Wales, Sydney, AustraliaSchool of Medical Sciences, University of New South Wales, Sydney, AustraliaDepartment of Physiology, University of New South Wales, Sydney, AustraliaSchool of Medical Sciences, University of New South Wales, Sydney, AustraliaSchool of Medical Sciences, University of New South Wales, Sydney, AustraliaSchool of Medical Sciences, University of New South Wales, Sydney, AustraliaPurpose: The purpose of this study was to determine the relative expression of clinically-relevant components of the renin-angiotensin system (RAS) in the adult human eye. Methods: We obtained 14 post-mortem enucleated human eyes from patients whom had no history of inflammatory ocular disease nor pre-mortem ocular infection. We determined the gene expression for prorenin, renin, prorenin receptor, angiotensin-converting enzyme, angiotensinogen and angiotensin II Type 1 receptor, on tissue sections and in cultured human primary retinal pigment epithelial and iris pigment epithelial (RPE/IPE) cell lines, using both qualitative and quantitative reverse transcription polymerase chain reaction (RT-PCR). Protein expression was studied using indirect immunofluorescence (IF). Results: Almost all components of the classical RAS were found at high levels, at both the transcript and protein level, in the eyes’ uvea and retina; and at lower levels in the cornea, conjunctiva and sclera. There was a much lower level of expression in the reference cultured RPE/IPE cells lines. Conclusion: This study describes the distribution of RAS in the normal adult human eye and demonstrates the existence of an independent ocular RAS, with uveal and retinal tissues showing the highest expression of RAS components. These preliminary findings provide scope for examination of additional components of this system in the human eye, as well as possible differential expression under pathological conditions.https://doi.org/10.1177/1470320314549791
collection DOAJ
language English
format Article
sources DOAJ
author Andrew JR White
Sarat C Cheruvu
Maria Sarris
Surabhi S Liyanage
Eugenie Lumbers
Jeanie Chui
Denis Wakefield
Peter J McCluskey
spellingShingle Andrew JR White
Sarat C Cheruvu
Maria Sarris
Surabhi S Liyanage
Eugenie Lumbers
Jeanie Chui
Denis Wakefield
Peter J McCluskey
Expression of classical components of the renin-angiotensin system in the human eye
Journal of the Renin-Angiotensin-Aldosterone System
author_facet Andrew JR White
Sarat C Cheruvu
Maria Sarris
Surabhi S Liyanage
Eugenie Lumbers
Jeanie Chui
Denis Wakefield
Peter J McCluskey
author_sort Andrew JR White
title Expression of classical components of the renin-angiotensin system in the human eye
title_short Expression of classical components of the renin-angiotensin system in the human eye
title_full Expression of classical components of the renin-angiotensin system in the human eye
title_fullStr Expression of classical components of the renin-angiotensin system in the human eye
title_full_unstemmed Expression of classical components of the renin-angiotensin system in the human eye
title_sort expression of classical components of the renin-angiotensin system in the human eye
publisher Hindawi - SAGE Publishing
series Journal of the Renin-Angiotensin-Aldosterone System
issn 1470-3203
1752-8976
publishDate 2015-03-01
description Purpose: The purpose of this study was to determine the relative expression of clinically-relevant components of the renin-angiotensin system (RAS) in the adult human eye. Methods: We obtained 14 post-mortem enucleated human eyes from patients whom had no history of inflammatory ocular disease nor pre-mortem ocular infection. We determined the gene expression for prorenin, renin, prorenin receptor, angiotensin-converting enzyme, angiotensinogen and angiotensin II Type 1 receptor, on tissue sections and in cultured human primary retinal pigment epithelial and iris pigment epithelial (RPE/IPE) cell lines, using both qualitative and quantitative reverse transcription polymerase chain reaction (RT-PCR). Protein expression was studied using indirect immunofluorescence (IF). Results: Almost all components of the classical RAS were found at high levels, at both the transcript and protein level, in the eyes’ uvea and retina; and at lower levels in the cornea, conjunctiva and sclera. There was a much lower level of expression in the reference cultured RPE/IPE cells lines. Conclusion: This study describes the distribution of RAS in the normal adult human eye and demonstrates the existence of an independent ocular RAS, with uveal and retinal tissues showing the highest expression of RAS components. These preliminary findings provide scope for examination of additional components of this system in the human eye, as well as possible differential expression under pathological conditions.
url https://doi.org/10.1177/1470320314549791
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