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ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis

BACKGROUND: Vascular endothelial cell (EC) alignment in the direction of flow is an adaptive response that protects against aortic diseases, such as atherosclerosis. The Rho GTPases are known to regulate this alignment. Herein, we analyze the effect of ARHGAP18 on the regulation of EC alignment and...

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Autores principales: Lay, Angelina J., Coleman, Paul R., Formaz‐Preston, Ann, Ting, Ka Ka, Roediger, Ben, Weninger, Wolfgang, Schwartz, Martin A., Vadas, Mathew A., Gamble, Jennifer R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497359/
https://www.ncbi.nlm.nih.gov/pubmed/30630384
http://dx.doi.org/10.1161/JAHA.118.010057
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author Lay, Angelina J.
Coleman, Paul R.
Formaz‐Preston, Ann
Ting, Ka Ka
Roediger, Ben
Weninger, Wolfgang
Schwartz, Martin A.
Vadas, Mathew A.
Gamble, Jennifer R.
author_facet Lay, Angelina J.
Coleman, Paul R.
Formaz‐Preston, Ann
Ting, Ka Ka
Roediger, Ben
Weninger, Wolfgang
Schwartz, Martin A.
Vadas, Mathew A.
Gamble, Jennifer R.
author_sort Lay, Angelina J.
collection PubMed
description BACKGROUND: Vascular endothelial cell (EC) alignment in the direction of flow is an adaptive response that protects against aortic diseases, such as atherosclerosis. The Rho GTPases are known to regulate this alignment. Herein, we analyze the effect of ARHGAP18 on the regulation of EC alignment and examine the effect of ARHGAP18 deficiency on the development of atherosclerosis in mice. METHODS AND RESULTS: We used in vitro analysis of ECs under flow conditions together with apolipoprotein E(−/−) Arhgap18 (−/−) double‐mutant mice to study the function of ARHGAP18 in a high‐fat diet–induced model of atherosclerosis. Depletion of ARHGAP18 inhibited the alignment of ECs in the direction of flow and promoted inflammatory phenotype, as evidenced by disrupted junctions and increased expression of nuclear factor‐κB and intercellular adhesion molecule‐1 and decreased endothelial nitric oxide synthase. Mice with double deletion in ARHGAP18 and apolipoprotein E and fed a high‐fat diet show early onset of atherosclerosis, with lesions developing in atheroprotective regions. CONCLUSIONS: ARHGAP18 is a protective gene that maintains EC alignments in the direction of flow. Deletion of ARHGAP18 led to loss of EC ability to align and promoted atherosclerosis development.
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spelling pubmed-64973592019-05-07 ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis Lay, Angelina J. Coleman, Paul R. Formaz‐Preston, Ann Ting, Ka Ka Roediger, Ben Weninger, Wolfgang Schwartz, Martin A. Vadas, Mathew A. Gamble, Jennifer R. J Am Heart Assoc Original Research BACKGROUND: Vascular endothelial cell (EC) alignment in the direction of flow is an adaptive response that protects against aortic diseases, such as atherosclerosis. The Rho GTPases are known to regulate this alignment. Herein, we analyze the effect of ARHGAP18 on the regulation of EC alignment and examine the effect of ARHGAP18 deficiency on the development of atherosclerosis in mice. METHODS AND RESULTS: We used in vitro analysis of ECs under flow conditions together with apolipoprotein E(−/−) Arhgap18 (−/−) double‐mutant mice to study the function of ARHGAP18 in a high‐fat diet–induced model of atherosclerosis. Depletion of ARHGAP18 inhibited the alignment of ECs in the direction of flow and promoted inflammatory phenotype, as evidenced by disrupted junctions and increased expression of nuclear factor‐κB and intercellular adhesion molecule‐1 and decreased endothelial nitric oxide synthase. Mice with double deletion in ARHGAP18 and apolipoprotein E and fed a high‐fat diet show early onset of atherosclerosis, with lesions developing in atheroprotective regions. CONCLUSIONS: ARHGAP18 is a protective gene that maintains EC alignments in the direction of flow. Deletion of ARHGAP18 led to loss of EC ability to align and promoted atherosclerosis development. John Wiley and Sons Inc. 2019-01-11 /pmc/articles/PMC6497359/ /pubmed/30630384 http://dx.doi.org/10.1161/JAHA.118.010057 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Lay, Angelina J.
Coleman, Paul R.
Formaz‐Preston, Ann
Ting, Ka Ka
Roediger, Ben
Weninger, Wolfgang
Schwartz, Martin A.
Vadas, Mathew A.
Gamble, Jennifer R.
ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis
title ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis
title_full ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis
title_fullStr ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis
title_full_unstemmed ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis
title_short ARHGAP18: A Flow‐Responsive Gene That Regulates Endothelial Cell Alignment and Protects Against Atherosclerosis
title_sort arhgap18: a flow‐responsive gene that regulates endothelial cell alignment and protects against atherosclerosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497359/
https://www.ncbi.nlm.nih.gov/pubmed/30630384
http://dx.doi.org/10.1161/JAHA.118.010057
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