Stem cell-derived extracellular vesicles mitigate ageing-associated arterial stiffness and hypertension

被引:65
作者
Feng, Rui [1 ]
Ullah, Mujib [2 ]
Chen, Kai [2 ]
Ali, Quaisar [2 ]
Lin, Yi [2 ]
Sun, Zhongjie [2 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Cardiol, Chongqing, Peoples R China
[2] Univ Tennessee, Ctr Hlth Sci, Coll Med, Dept Physiol, Memphis, TN 38163 USA
基金
美国国家卫生研究院;
关键词
Extracellular vesicles; stem cell; arterial stiffness; hypertension; SIRT1; AMPK; CHRONIC KIDNEY-DISEASE; ANTIAGING GENE KLOTHO; SMOOTH-MUSCLE-CELL; BLOOD-PRESSURE; CARDIOVASCULAR-DISEASE; AORTIC STIFFNESS; RISK-FACTOR; DEFICIENCY; ACTIVATION; FIBROSIS;
D O I
10.1080/20013078.2020.1783869
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The prevalence of arterial stiffness and hypertension increases with age. This study investigates the effect of induced pluripotent mesenchymal stem cell-derived extracellular vesicles (EVs) on ageing-associated arterial stiffness and hypertension. EVs were collected and purified from induced pluripotent stem cell-derived mesenchymal stem cells (iPS-MSCs). Young and old male C57BU6 mice were used. Mice in the EVs group were injected via tail vein once a week for four weeks (18 x 10(6) EVs/mouse/injection). Blood pressure (BP) was measured using the tail-cuff method and validated by direct cannulation. Pulse wave velocity (PWV) was measured using a Doppler workstation. PWV and BP were increased significantly in the old mice, indicating arterial stiffness and hypertension. Intravenous administration of EVs significantly attenuated ageing-related arterial stiffness and hypertension, while enhancing endothelium-dependent vascular relaxation and arterial compliance in the old EVs mice. Elastin degradation and collagen I deposition (fibrosis) were increased in aortas of the old mice, but EVs substantially improved ageing-associated structural remodelling. Mechanistically, EVs abolished downregulation of sirtuin type 1 (SIRT1), and endothelial nitric oxide synthase (eNOS) protein expression in aortas of the older mice. In cultured human aortic endothelial cells, EVs promoted the expression of SIRT1, AMP-activated protein kinase alpha (AMPKa), and eNOS. In conclusion, iPS-MSC-derived EVs attenuated ageing-associated vascular endothelial dysfunction, arterial stiffness, and hypertension, likely via activation of the SIRT1-AMPK alpha-eNOS pathway and inhibition of MMPs and elastase. Thus, EVs mitigate arterial ageing. This finding also sheds light into the therapeutic potential of EVs for ageing-related vascular diseases.
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页数:13
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