Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation

Abstract Cyr61 is a member of the CCN family of proteins that is expressed in atherosclerotic lesions and regulated by angiotensin II. It is unknown whether renal artery stenosis (RAS) increases Cyr61 expression. Male ApoE−/− mice were randomized to surgically induced RAS, RAS + treatment with eithe...

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Main Authors: Alokkumar S. Pathak, Mauricio Rojas, George A. Stouffer
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-81646-1
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spelling doaj-3821fd40f44746c6aecf9ba0bd0c07042021-02-14T12:32:59ZengNature Publishing GroupScientific Reports2045-23222021-02-0111111010.1038/s41598-021-81646-1Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligationAlokkumar S. Pathak0Mauricio Rojas1George A. Stouffer2McAllister Heart Institute, University of North CarolinaMcAllister Heart Institute, University of North CarolinaMcAllister Heart Institute, University of North CarolinaAbstract Cyr61 is a member of the CCN family of proteins that is expressed in atherosclerotic lesions and regulated by angiotensin II. It is unknown whether renal artery stenosis (RAS) increases Cyr61 expression. Male ApoE−/− mice were randomized to surgically induced RAS, RAS + treatment with either irbesartan, aliskiren or amlodipine or sham-surgery. RAS resulted in increased plasma angiotensin II levels, a mild, sustained increase in systolic blood pressure and increased aortic lipid deposition compared to sham-surgery. Surgically induced RAS led to the formation of atheroma in the infrarenal aorta and there was consistent and intense staining for Cyr61 within the atheroma. Treatment with irbesartan, aliskiren and amlodipine were associated with decreased aortic lipid deposition and decreased staining for Cyr61 in aortic atheroma. Serum levels of Cyr61 were not increased in mice or humans with RAS. In summary, Cyr61 expression in aortic atheroma but not serum is increased by RAS in ApoE−/− mice and is reduced by agents that lower blood pressure.https://doi.org/10.1038/s41598-021-81646-1
collection DOAJ
language English
format Article
sources DOAJ
author Alokkumar S. Pathak
Mauricio Rojas
George A. Stouffer
spellingShingle Alokkumar S. Pathak
Mauricio Rojas
George A. Stouffer
Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation
Scientific Reports
author_facet Alokkumar S. Pathak
Mauricio Rojas
George A. Stouffer
author_sort Alokkumar S. Pathak
title Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation
title_short Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation
title_full Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation
title_fullStr Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation
title_full_unstemmed Expression of Cyr61 in ApoE−/− mice with chronic unilateral renal artery ligation
title_sort expression of cyr61 in apoe−/− mice with chronic unilateral renal artery ligation
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-02-01
description Abstract Cyr61 is a member of the CCN family of proteins that is expressed in atherosclerotic lesions and regulated by angiotensin II. It is unknown whether renal artery stenosis (RAS) increases Cyr61 expression. Male ApoE−/− mice were randomized to surgically induced RAS, RAS + treatment with either irbesartan, aliskiren or amlodipine or sham-surgery. RAS resulted in increased plasma angiotensin II levels, a mild, sustained increase in systolic blood pressure and increased aortic lipid deposition compared to sham-surgery. Surgically induced RAS led to the formation of atheroma in the infrarenal aorta and there was consistent and intense staining for Cyr61 within the atheroma. Treatment with irbesartan, aliskiren and amlodipine were associated with decreased aortic lipid deposition and decreased staining for Cyr61 in aortic atheroma. Serum levels of Cyr61 were not increased in mice or humans with RAS. In summary, Cyr61 expression in aortic atheroma but not serum is increased by RAS in ApoE−/− mice and is reduced by agents that lower blood pressure.
url https://doi.org/10.1038/s41598-021-81646-1
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