Endothelial Foxp1 Suppresses Atherosclerosis via Modulation of Nlrp3 Inflammasome Activation

Endothelial Foxp1 Suppresses Atherosclerosis via Modulation of Nlrp3 Inflammasome Activation.

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Item Type: Article
Status: Published
Official URL: https://doi.org/10.1161/CIRCRESAHA.118.314402
Journal or Publication Title: Circulation Research
Volume: 125
Number: 6
Page Range: pp. 590-605
Date: 2019
Divisions: Cell Signalling
Depositing User: General Admin
Identification Number: 10.1161/CIRCRESAHA.118.314402
ISSN: 0009-7330
Date Deposited: 21 Dec 2020 23:13
Abstract:

Rationale: Endothelial dysfunction results in sustained and chronic vascular inflammation, which is central to atherosclerotic diseases. However, transcriptional regulation of vascular endothelial inflammation has not been well clarified.

Objective: This study aims to explore Foxp (forkhead box P) transcription factor 1 in regulation of endothelial homeostasis, atherogenesis, and its mechanisms.

Methods and results: To assess the importance of Foxp1 in atherosclerosis, Foxp1 expression was analyzed in human coronary artery and mouse artery, and we observed significant downregulation of Foxp1 in atherosclerotic and atherosusceptible endothelium. Endothelial-specific Foxp1 knockout mice (Foxp1ECKO) were bred onto ApoeKO mice to generate endothelial Foxp1-deletion hyperlipidemic model Foxp1ECKO;ApoeKO, which displayed significant increases in atherosclerotic lesion formation in aortas and aortic roots with enhanced monocyte adhesion, migration, and infiltration into the vascular wall and formation of inflammatory lipid-laden macrophages. In contrast, endothelial-specific Foxp1 overexpression mice Foxp1ECTg;ApoeKO exhibited reduced atherosclerotic lesion formation with less monocyte infiltration. Foxp1 was further identified as a gatekeeper of vessel inflammation by direct regulation of endothelial inflammasome components, including Nlrp3 (NLR [nucleotide-binding and leucine-rich repeat immune receptors] family pyrin domain containing 3), caspase-1, and IL (interleukin)-1β. Moreover, endothelial Foxp1 was found to be regulated by Klf2 (Kruppel-like factor 2). Oscillatory shear stress downregulated Foxp1 expression via repressing Klf2 expression in endothelium, and, therefore, promoted endothelial inflammasome activation, leading to atherosclerotic lesion formation. Simvastatin upregulated the reduced expression of Klf2 and Foxp1 in atherosusceptible vascular endothelium and alleviated vascular inflammation contributing to its inhibitory effect in atherosclerosis.

Conclusions: These data are the first in vivo experimental validation of an atheroprotective role of endothelial Klf2 and Foxp1, which reveals a Klf2-Foxp1 transcriptional network in endothelial cells as a novel regulator of endothelial inflammasome activation for atherogenesis, therefore, provides opportunities for therapeutic intervention of atherosclerotic diseases and uncovers a novel atheroprotective mechanism for simvastatin.

Keywords: atherosclerosis; endothelium; inflammasome; mice; simvastatin.

Creators:
Creators
Email
Zhuang, Tao
UNSPECIFIED
Liu, Jie
UNSPECIFIED
Chen, Xiaoli
UNSPECIFIED
Zhang, Lin
UNSPECIFIED
Pi, Jingjiang
UNSPECIFIED
Sun, Huimin
UNSPECIFIED
Li, Li
UNSPECIFIED
Bauer, Robert
UNSPECIFIED
Wang, Haikun
UNSPECIFIED
Yu, Zuoren
UNSPECIFIED
Zhang, Qi
UNSPECIFIED
Tomlinson, Brian
UNSPECIFIED
Chan, Paul
UNSPECIFIED
Zheng, Xiangjian
UNSPECIFIED
Morrisey, Edward
UNSPECIFIED
Liu, Zhongmin
UNSPECIFIED
Reilly, Muredach
UNSPECIFIED
Zhang, Yuzhen
UNSPECIFIED
Last Modified: 21 Dec 2020 23:13
URI: https://eprints.centenary.org.au/id/eprint/151

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