Tsakiroglou Panagiotis, Weber James, Ashworth Sharon, Del Bo Cristian, Klimis-Zacas Dorothy
School of Food and Agriculture, University of Maine, Orono, Maine.
School of Biology and Ecology, University of Maine, Orono, Maine.
J Cell Biochem. 2019 Jul;120(7):11056-11067. doi: 10.1002/jcb.28383. Epub 2019 Jan 30.
The present study investigates the effect of anthocyanin (ACN), phenolic acid (PA) fractions, and their combination (ACNs:PAs) from wild blueberry powder (Vaccinum angustifolium) on the speed of endothelial cell migration, gene expression, and protein levels of RAC1 and RHOA associated with acute exposure to different concentrations of ACNs and PAs. Time-lapse videos were analyzed and endothelial cell speed was calculated. Treatment with ACNs at 60 μg/mL inhibited endothelial cell migration rate ( P ≤ 0.05) while treatment with PAs at 0.002 μg/mL ( P ≤ 0.0001), 60 μg/mL ( P ≤ 0.0001), and 120 μg/mL ( P ≤ 0.01) significantly increased endothelial cell migration rate compared with control. Moreover, exposure of HUVECs to ACNs:PAs at 8:8 μg/mL ( P ≤ 0.05) and 60:60 μg/mL increased ( P ≤ 0.001) endothelial cell migration. Gene expression of RAC1 and RHOA significantly increased 2 hours after exposure with all treatments. No effect of the above fractions was observed on the protein levels of RAC1 and RHOA. Findings suggest that endothelial cell migration is differentially modulated based on the type of blueberry extract (ACN or PA fraction) and is concentration-dependent. Future studies should determine the mechanism of the differential action of the above fractions on endothelial cell migration.
本研究调查了野生蓝莓粉(狭叶越橘)中的花青素(ACN)、酚酸(PA)组分及其组合(ACNs:PAs)对内皮细胞迁移速度、基因表达以及与急性暴露于不同浓度ACNs和PAs相关的RAC1和RHOA蛋白水平的影响。分析了延时视频并计算了内皮细胞速度。用60μg/mL的ACNs处理可抑制内皮细胞迁移率(P≤0.05),而用0.002μg/mL(P≤0.0001)、60μg/mL(P≤0.0001)和120μg/mL(P≤0.01)的PAs处理与对照组相比显著提高了内皮细胞迁移率。此外,将人脐静脉内皮细胞(HUVECs)暴露于8:8μg/mL(P≤0.05)和60:60μg/mL的ACNs:PAs中可增加(P≤0.001)内皮细胞迁移。所有处理暴露2小时后,RAC1和RHOA的基因表达均显著增加。未观察到上述组分对RAC1和RHOA蛋白水平有影响。研究结果表明,内皮细胞迁移根据蓝莓提取物的类型(ACN或PA组分)受到不同调节,且具有浓度依赖性。未来的研究应确定上述组分对内皮细胞迁移产生差异作用的机制。