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The FASEB Journal
Article
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DIGITAL.CSIC
Article . 2019 . Peer-reviewed
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The FASEB Journal
Article . 2019 . Peer-reviewed
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Regulation and role of endoglin in cholesterol‐induced endothelial and vascular dysfunction in vivo and in vitro

Authors: Vicen, Matej; Vitverova, Barbora; Havelek, Radim; Blazickova, Katerina; Machacek, Miloslav; Rathouska, Jana; Najmanová, Iveta; +5 Authors

Regulation and role of endoglin in cholesterol‐induced endothelial and vascular dysfunction in vivo and in vitro

Abstract

ABSTRACT Our objective was to investigate the effect of cholesterol [hypercholesterolemia and 7‐ketocholesterol (7K)] on endoglin (Eng) expression and regulation with respect to endothelial or vascular dysfunction in vivo and in vitro. In vivo experiments were performed in 2‐mo‐old atherosclerosis‐prone apolipoprotein E–deficient/LDL receptor–deficient (ApoE −/− /LDLR −/− ) female mice and their wild‐type C57BL/6J littermates. In in vitro experiments, human aortic endothelial cells (HAECs) were treated with 7K. ApoE −/− /LDLR −/− mice developed hypercholesterolemia accompanied by increased circulating levels of P‐selectin and Eng and a disruption of NO metabolism. Functional analysis of the aorta demonstrated impaired vascular reactivity, and Western blot analysis revealed down‐regulation of membrane Eng/Smad2/3/eNOS signaling in ApoE −/− /LDLR −/− mice. 7K increased Eng expression via Krüppel‐like factor 6 (KLF6), liver X nuclear receptor, and NF‐&x03BA;B in HAECs. 7K‐induced Eng expression was prevented by the treatment with 2‐hydroxypropyl‐β‐cyclodextrin; 8‐{[5‐chloro‐2‐(4‐methylpiperazin‐1‐ yl ) pyridine‐4‐carbonyl] amino}‐1‐(4‐fluorophenyl)‐4, 5‐dihydrobenzo[g]indazole‐3‐carboxamide; or by KLF6 silencing. 7K induced increased adhesion and transmigration of monocytic human leukemia promonocytic cell line cells and was prevented by Eng silencing. We concluded that hypercholesterolemia altered Eng expression and signaling, followed by endothelial or vascular dysfunction before formation of atherosclerotic lesions in ApoE −/− /LDLR −/− mice. By contrast, 7K increased Eng expression and induced inflammation in HAECs, which was followed by an increased adhesion and transmigration of monocytes via endothelium, which was prevented by Eng inhibition. Thus, we propose a relevant role for Eng in endothelial or vascular dysfunction or inflammation when exposed to cholesterol.—Vicen, M., Vitverova, B., Havelek, R., Blazickova, K., Machacek, M., Rathouska, J., Najmanová, I., Dolezelova, E., Prasnicka, A., Sternak, M., Bernabeu, C, Nachtigal, P. Regulation and role of endoglin in cholesterol‐induced endothelial and vascular dysfunction in vivo and in vitro . FASEB J. 33, 6099–6114 (2019). www.fasebj.org

Countries
Poland, Spain
Keywords

Indazoles, Nitric Oxide Synthase Type III, Hypercholesterolemia, Nitric Oxide, Mice, Apolipoproteins E, Kruppel-Like Factor 6, Animals, Humans, Endothelial dysfunction, Aorta, Cells, Cultured, Endoglin, NF-kappa B, Oxysterols, Plaque, Atherosclerotic, Mice, Inbred C57BL, P-Selectin, Cholesterol, Female, Endothelium, Vascular, Isonicotinic Acids

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
views
OpenAIRE UsageCountsViews provided by UsageCounts
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22
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60
106
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