Doxorubicin-induced cardiomyocyte toxicity – protective effects of endothelial cells in a tri-culture model system

Eliesmaziah Alias, Vijay Parikh, Araida Hidalgo-Bastida, Malcolm Wilkinson, Kelly S. Davidge, Tim Gibson, Duncan Sharp, Rameen Shakur, May Azzawi
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引用次数: 3

Abstract

Doxorubicin-induced cardiomyopathy is a clinically prevalent pathology, occurring as a sequelae following chemotherapy for cancer patients. In particular, the “first dose” effect has been particularly challenging, given the heterogeneous and multifactorial nature of this pathophysiology. Here, we describe the development of a physiologically relevant in vitro model for cardiotoxicity testing, using human cells. Primary cardiomyocytes, endothelial, and smooth muscle cells were tri-cultured in 2D, or within nano-fibrous scaffolds in a 3D environment, under dynamic nutrient flow, using the Quasi Vivo® system. State-of-the-art sensor chips were used to detect troponin I levels, 2 h after acute exposure to doxorubicin. We demonstrate a significant improvement in cardiomyocyte viability when grown in a 3D tri-culture environment over a 5-day period and a 10-fold reduction in doxorubicin-induced toxicity. Our tri-culture model can be used as a valuable tool for physiologically relevant assessment of drug-induced cardiotoxicity in vitro.

Abstract Image

阿霉素诱导心肌细胞毒性-内皮细胞在三培养模型系统中的保护作用
阿霉素诱导的心肌病是一种临床上普遍存在的病理,是癌症患者化疗后的后遗症。特别是,考虑到这种病理生理学的异质性和多因素性质,“首次剂量”效应尤其具有挑战性。在这里,我们描述了一个生理相关的心脏毒性测试的体外模型的发展,使用人类细胞。使用Quasi Vivo®系统,原代心肌细胞、内皮细胞和平滑肌细胞在二维环境中进行三次培养,或在三维环境中在纳米纤维支架中进行动态营养流动培养。在急性暴露于阿霉素2小时后,使用最先进的传感器芯片检测肌钙蛋白I水平。我们证明,在3D三种培养环境中培养5天后,心肌细胞活力显著提高,阿霉素诱导的毒性降低了10倍。我们的三培养模型可以作为体外药物诱导心脏毒性生理相关评估的有价值的工具。
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