Journal
ATHEROSCLEROSIS
Volume 328, Issue -, Pages 83-91Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2021.05.019
Keywords
Atherosclerosis; Apolipoprotein A-I mimetic peptide; Tetrahydrobiopterin; GTP-Cyclohydrolase 1; Endothelial nitric oxide synthase; Heat shock protein 90
Funding
- National Natural Science Foundation of China [81830013, 81970363, 81370370, 81670392, 81600382, 81770241, 82000362]
- Guangzhou Major Research Program [202103000016]
- Guangdong Natural Science Fund Committee [2015A030312009]
- Guangdong Basic and Applied Basic Research Foundation [2019B1515120092]
- Sun Yatsen University Clinical Research 5010 Program [2014002]
- Program of National Key Clinical Specialties
- Changjiang Scholars Program from the Ministry of Education of China
- Fundamental Research Funds for the Central Universities Sun Yatsen University Young Teacher Training Program [19ykpy79]
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The study revealed that hypercholesterolemia increases uncoupled eNOS activity by reducing GCH-1 concentration, leading to lower BH4 levels. D-4F reduces uncoupled eNOS activity by increasing BH4 levels through GCH-1 expression and by decreasing eNOS phosphorylation and eNOS-HSP90 association.
Background and aims: The apolipoprotein A-I mimetic peptide D-4F, among its anti-atherosclerotic effects, improves vasodilation through mechanisms not fully elucidated yet. Methods: Low-density lipoprotein (LDL) receptor null (LDLr-/-) mice were fed Western diet with or without D-4F. We then measured atherosclerotic lesion formation, endothelial nitric oxide synthase (eNOS) phosphorylation and its association with heat shock protein 90 (HSP90), nitric oxide (NO) and superoxide anion (O-2(center dot-)) production, and tetrahydrobiopterin (BH4) and GTP-cyclohydrolase 1 (GCH-1) concentration in the aorta. Human umbilical vein endothelial cells (HUVECs) and aortas were treated with oxidized LDL (oxLDL) with or without D-4F; subsequently, BH4 and GCH-1 concentration, NO and O-2(center dot-) production, eNOS association with HSP90, and endothelium-dependent vasodilation were measured. Results: Unexpectedly, eNOS phosphorylation, eNOS-HSP90 association, and O-2(center dot-) production were increased, whereas BH4 and GCH-1 concentration and NO production were reduced in atherosclerosis. D-4F significantly inhibited atherosclerosis, eNOS phosphorylation, eNOS-HSP90 association, and O-2(center dot-) generation but increased NO production and BH4 and GCH-1 concentration. OxLDL reduced NO production and BH4 and GCH-1 concentration but enhanced O-2(center dot-) generation and eNOS association with HSP90, and impaired endothelium-dependent vasodilation. D-4F inhibited the overall effects of oxLDL. Conclusions: Hypercholesterolemia enhanced uncoupled eNOS activity by decreasing GCH-1 concentration, thereby reducing BH4 levels. D-4F reduced uncoupled eNOS activity by increasing BH4 levels through GCH-1 expression and decreasing eNOS phosphorylation and eNOS-HSP90 association. Our findings elucidate a novel mechanism by which hypercholesterolemia induces atherosclerosis and D-4F inhibits it, providing a potential therapeutic approach.
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