Abstract

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 µM docosahexaenoic acid or eicosapentaenoic acid for 5 days at 37 °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.

Highlights

  • Endothelial dysfunction, a corollary of hypertension, contributes to the development of inflammation and atherosclerosis [1]

  • Immunoreactive staining for von Willebrand factor (vWF) was observed in human umbilical vein endothelial cells (HUVECs), and this was localized to rod-shaped Weibel-Palade bodies (WPBs) within the cytoplasm (Figure 1b)

  • We investigated whether eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) could affect actin cytoskeletal reorganization associated with WPB degranulation in human endothelial cells

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Summary

Introduction

Endothelial dysfunction, a corollary of hypertension, contributes to the development of inflammation and atherosclerosis [1]. It has further been shown that stimulation of human umbilical vein endothelial cells (HUVECs) with PMA results in longitudinal stress fiber formation as well as recruitment of actin filaments to WPBs undergoing exocytosis [14]. One possibility is that LC n-3 PUFAs attenuate the release of pre-stored substances from the endothelium to decrease circulating concentrations of pro-inflammatory mediators such as vWF. To test this hypothesis, we treated cultured HUVECs with LC n-3 PUFAs, docosahexaenoic acid (DHA) or eicosapentaenoic acid (EPA), and examined their ability to attenuate PMA-stimulated WPB degranulation as well as their effects on actin rearrangement

PMA-Stimulated Degranulation of Weibel-Palade Bodies
Culture of Human Umbilical Vein Endothelial Cells
Immunocytochemistry Staining for Von Willebrand Factor
Quantitation of Weibel-Palade Body Degranulation
Gas Chromatography—Mass Spectrometry Analysis of Cellular LC n-3 PUFA
Oil Red O Staining for Lipids
Cellular Actin Remodeling
Conclusions
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