The Protective Effects of Tripeptides VPP and IPP against Small Extracellular Vesicles from Angiotensin II-Induced Vascular Smooth Muscle Cells Mediating Endothelial Dysfunction in Human Umbilical Vein Endothelial Cells
文献类型: 外文期刊
作者: Song, Tianyuan 1 ; Lv, Miao 1 ; Zhang, Lixia 3 ; Zhang, Xun 3 ; Song, Guohui 3 ; Huang, Mingtao 1 ; Zheng, Lin 1 ; Zhao, 1 ;
作者机构: 1.South China Univ Technol, Sch Food Sci & Engn, Guangzhou 510640, Peoples R China
2.Guangdong Food Green Proc & Nutr Regulat Technol, Guangzhou 510640, Peoples R China
3.Henan Acad Agr Sci, Inst Agr Prod Proc, Zhengzhou 450002, Peoples R China
关键词: antihypertensive peptides; angiotensin II; extracellular vesicles; endothelial dysfunction; 3D cell cultures
期刊名称:JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY ( 影响因子:5.279; 五年影响因子:5.269 )
ISSN: 0021-8561
年卷期: 2020 年 68 卷 47 期
页码:
收录情况: SCI
摘要: Endothelial dysfunction is a common disorder of vascular homeostasis in hypertension characterized by oxidative stress, malignant migration, inflammatory response, and active adhesion response of endothelial cells. The extracellular vesicles (EVs), a vital participant in vascular cell communication, have been considered responsible for vascular disease progression. However, the potential mechanism of antihypertensive peptides against the EVs-induced endothelial dysfunction is still unclear. In this study, we investigated whether the antihypertensive peptides Val-Pro-Pro (VPP) and Ile-Pro-Pro (IPP) ameliorate the effects of EVs from Ang II-induced vascular smooth muscles (VSMCs) on the endothelial dysfunction. The dihydroethidium staining, wound healing assay, 3D cell culture, and co-culture with U937 monocyte were used to investigate the oxidant/antioxidant balance, migration, tube formation, and cell adhesion in EV-induced human umbilical vein endothelial cells. VPP and IPP treatment reduced the level of reactive oxygen species and EV-induced expression of adhesion molecules and restored the ability of tube formation by upregulating endothelial nitric oxide synthase expression. VPP and IPP reduced the protein levels of IL-6 to 227.34 +/- 10.56 and 273.84 +/- 22.28 pg/mL, of IL-1 beta protein to 131.56 +/- 23.18 and 221.14 +/- 13.8 pg/mL, and of MCP-1 to 301.48 +/- 19.75 and 428.68 +/- 9.59 pg/mL. These results suggested that the VPP and IPP are potential agents that can improve the endothelial dysfunction caused by EVs from Ang II-induced VSMCs.
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