Cameron Scott J, Morrell Craig N, Bao Clare, Swaim AnneMarie F, Rodriguez Annabelle, Lowenstein Charles J
Departments of Medicine, Division of Cardiology, University of Rochester School of Medicine, Box 679, 601 Elmwood Avenue, Rochester, NY, 14652, United States of America.
Aab Cardiovascular Research Institute, University of Rochester School of Medicine, Box CVRI, 601 Elmwood Avenue, Rochester, NY, 14652, United States of America.
PLoS One. 2015 Dec 17;10(12):e0144372. doi: 10.1371/journal.pone.0144372. eCollection 2015.
High density lipoprotein has anti-inflammatory effects in addition to mediating reverse cholesterol transport. While many of the chronic anti-inflammatory effects of high density lipoprotein (HDL) are attributed to changes in cell adhesion molecules, little is known about acute signal transduction events elicited by HDL in endothelial cells. We now show that high density lipoprotein decreases endothelial cell exocytosis, the first step in leukocyte trafficking. ApoA-I, a major apolipoprotein of HDL, mediates inhibition of endothelial cell exocytosis by interacting with endothelial scavenger receptor-BI which triggers an intracellular protective signaling cascade involving protein kinase C (PKC). Other apolipoproteins within the HDL particle have only modest effects upon endothelial exocytosis. Using a human primary culture of endothelial cells and murine apo-AI knockout mice, we show that apo-AI prevents endothelial cell exocytosis which limits leukocyte recruitment. These data suggest that high density lipoprotein may inhibit diseases associated with vascular inflammation in part by blocking endothelial exocytosis.
高密度脂蛋白除了介导胆固醇逆向转运外,还具有抗炎作用。虽然高密度脂蛋白(HDL)的许多慢性抗炎作用归因于细胞黏附分子的变化,但对于HDL在内皮细胞中引发的急性信号转导事件却知之甚少。我们现在发现,高密度脂蛋白可减少内皮细胞胞吐作用,这是白细胞迁移的第一步。载脂蛋白A-I(ApoA-I)是HDL的主要载脂蛋白,它通过与内皮清道夫受体BI相互作用来介导对内皮细胞胞吐作用的抑制,后者触发了一个涉及蛋白激酶C(PKC)的细胞内保护信号级联反应。HDL颗粒中的其他载脂蛋白对内皮细胞胞吐作用的影响较小。利用人内皮细胞原代培养物和小鼠载脂蛋白A-I基因敲除小鼠,我们发现载脂蛋白A-I可防止内皮细胞胞吐作用,从而限制白细胞募集。这些数据表明,高密度脂蛋白可能部分通过阻断内皮细胞胞吐作用来抑制与血管炎症相关的疾病。