Selected article for: "cell study and endothelial cell"

Author: Teng, Dayu; Pannell, Jeffrey Scott; Rennert, Robert C; Li, Jieying; Li, Yi-Shuan; Wong, Victor W; Chien, Shu; Khalessi, Alexander A
Title: Endothelial trauma from mechanical thrombectomy in acute stroke: in vitro live-cell platform with animal validation.
  • Cord-id: nbnhjc6y
  • Document date: 2015_1_1
  • ID: nbnhjc6y
    Snippet: 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 endovasc
    Document: 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.

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