期刊
JOURNAL OF THE AMERICAN HEART ASSOCIATION
卷 7, 期 4, 页码 -出版社
WILEY
DOI: 10.1161/JAHA.117.008187
关键词
atherosclerosis; ATP-binding cassette transporter ABCA1; bone marrow transplant; foam cells; GW311616A; inflammation; macrophage; neutrophil elastase; neutrophil elastase inhibitor; protease
资金
- British Heart Foundation [FS/09/044/28007, PG/11/40/28891, PG/13/45/30326, PG/15/11/31279, PG/15/86/31723, PG/16/1/31892]
- National Funds for Developing Local College and Universities [B16056001]
- Wellcome Trust [098291/Z/12/Z]
- British Heart Foundation [PG/15/11/31279, FS/09/044/28007, PG/11/40/28891, PG/13/45/30326, PG/15/86/31723, PG/16/1/31892] Funding Source: researchfish
- Medical Research Council [1650315] Funding Source: researchfish
BackgroundTo investigate whether neutrophil elastase (NE) plays a causal role in atherosclerosis, and the molecular mechanisms involved. Methods and ResultsNE genetic-deficient mice (Apolipoprotein E-/-/NE-/- mice), bone marrow transplantation, and a specific NE inhibitor (GW311616A) were employed in this study to establish the causal role of NE in atherosclerosis. Aortic expression of NE mRNA and plasma NE activity was significantly increased in high-fat diet (HFD)-fed wild-type (WT) (Apolipoprotein E-/-) mice but, as expected, not in NE-deficient mice. Selective NE knockout markedly reduced HFD-induced atherosclerosis and significantly increased indicators of atherosclerotic plaque stability. While plasma lipid profiles were not affected by NE deficiency, decreased levels of circulating proinflammatory cytokines and inflammatory monocytes (Ly6C(hi)/CD11b(+)) were observed in NE-deficient mice fed with an HFD for 12weeks as compared with WT. Bone marrow reconstitution of WT mice with NE-/- bone marrow cells significantly reduced HFD-induced atherosclerosis, while bone marrow reconstitution of NE-/- mice with WT bone marrow cells restored the pathological features of atherosclerotic plaques induced by HFD in NE-deficient mice. In line with these findings, pharmacological inhibition of NE in WT mice through oral administration of NE inhibitor GW311616A also significantly reduced atherosclerosis. Mechanistically, we demonstrated that NE promotes foam cell formation by increasing ATP-binding cassette transporter ABCA1 protein degradation and inhibiting macrophage cholesterol efflux. ConclusionsWe outlined a pathogenic role for NE in foam cell formation and atherosclerosis development. Consequently, inhibition of NE may represent a potential therapeutic approach to treating cardiovascular disease.
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