Endothelial Trauma From Mechanical Thrombectomy in Acute Stroke In Vitro Live-Cell Platform With Animal Validation

被引:119
作者
Teng, Dayu [2 ,3 ]
Pannell, Jeffrey Scott [1 ]
Rennert, Robert C. [1 ]
Li, Jieying [2 ,3 ]
Li, Yi-Shuan [2 ,3 ]
Wong, Victor W. [1 ]
Chien, Shu [2 ,3 ]
Khalessi, Alexander A. [1 ]
机构
[1] Univ Calif San Diego, Div Neurosurg, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Dept Bioengn, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Inst Engn Med, San Diego, CA 92103 USA
关键词
endothelial cells; stroke; ENDOVASCULAR TREATMENT; VE-CADHERIN; SHEAR; FLOW; REVASCULARIZATION; EXPRESSION; JUNCTIONS; THERAPY; DEVICE; TRIAL;
D O I
10.1161/STROKEAHA.114.007494
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Endovascular thrombectomy has shown promise for the treatment of acute strokes resulting from large-vessel occlusion. Reperfusion-related injury may contribute to the observed decoupling of angiographic and clinical outcomes. Iatrogenic disruption of the endothelium during thrombectomy is potentially a key mediator of this process that requires further study. Methods-An in vitro live-cell platform was developed to study the effect of various commercially available endovascular devices on the endothelium. In vivo validation was performed using porcine subjects. Results-This novel in vitro platform permitted high-resolution quantification and characterization of the pattern and timing of endothelial-cell injury among endovascular thrombectomy devices and vessel diameters. Thrombectomy devices displayed heterogeneous effects on the endothelium; the device performance assessed in vitro was substantiated by in vivo findings. Conclusions-In vitro live-cell artificial vessel modeling enables a detailed study of the endothelium after thrombectomy and may contribute to future device design. Large animal studies confirm the relevance of this in vitro system to investigate endothelial physiology. This artificial vessel model may represent a practical, scalable, and physiologically relevant system to assess new endovascular technologies.
引用
收藏
页码:1099 / +
页数:12
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