Department for BioMedical Research, University of Bern, Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
Sci Rep. 2018 Apr 12;8(1):5898. doi: 10.1038/s41598-018-24273-7.
In the context of xenotransplantation, in ischemia/reperfusion injury as well as in cardiovascular research, the study of the fascinating interplay between endothelial cells (EC) and the plasma cascade systems often requires in vitro models. Blood vessels are hardly reproducible with standard flat-bed culture systems and flow-plate assays are limited in their low surface-to-volume ratio which impedes the study of the anticoagulant properties of the endothelial cells. According to the 3R regulations (reduce, replace and refine animal experimentation) we developed a closed circuit microfluidic in vitro system in which endothelial cells are cultured in 3D round section microchannels and subjected to physiological, pulsatile flow. In this study, a 3D monolayer of porcine aortic EC was perfused with human serum to mimic a xenotransplantation setting. Complement as well as EC activation was assessed in the presence or absence of complement inhibitors showing the versatility of the model for drug testing. Complement activation products as well as E-selectin expression were detected and visualized in situ by high resolution confocal microscopy. Furthermore, porcine pro-inflammatory cytokines as well as soluble complement components in the recirculating fluid phase were detected after human serum perfusion providing a better overview of the artificial vascular environment.
在异种移植、缺血/再灌注损伤以及心血管研究的背景下,内皮细胞(EC)与血浆级联系统之间迷人的相互作用研究通常需要体外模型。标准的平面培养系统很难再现血管,而流动板测定法由于其低的表面积与体积比而受到限制,这阻碍了对内皮细胞抗凝特性的研究。根据 3R 法规(减少、替代和优化动物实验),我们开发了一种封闭的循环微流控体外系统,其中内皮细胞在 3D 圆形截面微通道中培养,并受到生理、脉动流的影响。在这项研究中,用人血清灌注猪主动脉 EC 的 3D 单层以模拟异种移植环境。在存在或不存在补体抑制剂的情况下评估补体和 EC 激活,显示出该模型在药物测试方面的多功能性。通过高分辨率共焦显微镜原位检测和可视化补体激活产物和 E-选择素的表达。此外,在用人血清灌注后,可在循环液相中检测到猪促炎细胞因子和可溶性补体成分,从而提供了对人工血管环境的更好概述。