Omega-3 Fatty Acids Modulate Weibel-Palade Body Degranulation and Actin Cytoskeleton Rearrangement in PMA-Stimulated Human Umbilical Vein Endothelial Cells

被引:12
|
作者
Buergin-Maunder, Corinna S. [1 ]
Brooks, Peter R. [1 ]
Russell, Fraser D. [1 ]
机构
[1] Univ Sunshine Coast, Inflammat & Healing Res Cluster, Sch Hlth & Sport Sci, Maroochydore, Qld 4556, Australia
来源
MARINE DRUGS | 2013年 / 11卷 / 11期
关键词
omega-3 fatty acids; von willebrand factor; weibel-palade bodies; endothelial function; actin cytoskeleton; VON-WILLEBRAND-FACTOR; POLYUNSATURATED FATTY-ACIDS; EICOSAPENTAENOIC ACID; BLOOD-PRESSURE; DOCOSAHEXAENOIC ACID; LIPID-COMPOSITION; P-SELECTIN; EXOCYTOSIS; BODIES; N-3;
D O I
10.3390/md11114435
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Long chain omega-3 polyunsaturated fatty acids (LC n-3 PUFAs) produce cardiovascular benefits by improving endothelial function. Endothelial cells store von Willebrand factor (vWF) in cytoplasmic Weibel-Palade bodies (WPBs). We examined whether LC n-3 PUFAs regulate WPB degranulation using cultured human umbilical vein endothelial cells (HUVECs). HUVECs were incubated with or without 75 or 120 mu M docosahexaenoic acid or eicosapentaenoic acid for 5 days at 37 degrees C. WPB degranulation was stimulated using phorbol 12-myristate 13-acetate (PMA), and this was assessed by immunocytochemical staining for vWF. Actin reorganization was determined using phalloidin-TRITC staining. We found that PMA stimulated WPB degranulation, and that this was significantly reduced by prior incubation of cells with LC n-3 PUFAs. In these cells, WPBs had rounded rather than rod-shaped morphology and localized to the perinuclear region, suggesting interference with cytoskeletal remodeling that is necessary for complete WPB degranulation. In line with this, actin rearrangement was altered in cells containing perinuclear WPBs, where cells exhibited a thickened actin rim in the absence of prominent cytoplasmic stress fibers. These findings indicate that LC n-3 PUFAs provide some protection against WBP degranulation, and may contribute to an improved understanding of the anti-thrombotic effects previously attributed to LC n-3 PUFAs.
引用
收藏
页码:4435 / 4450
页数:16
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