Oleaga Carlota, Bernabini Catia, Smith Alec S T, Srinivasan Balaji, Jackson Max, McLamb William, Platt Vivien, Bridges Richard, Cai Yunqing, Santhanam Navaneetha, Berry Bonnie, Najjar Sarah, Akanda Nesar, Guo Xiufang, Martin Candace, Ekman Gail, Esch Mandy B, Langer Jessica, Ouedraogo Gladys, Cotovio Jose, Breton Lionel, Shuler Michael L, Hickman James J
NanoScience Technology Center, University of Central Florida, 12424 Research Parkway Suite 400, Orlando, FL 32828.
Department of Biomedical Engineering, Cornell University, 115 and 305 Weill Hall, Ithaca, NY 14853.
Sci Rep. 2016 Feb 3;6:20030. doi: 10.1038/srep20030.
We report on a functional human model to evaluate multi-organ toxicity in a 4-organ system under continuous flow conditions in a serum-free defined medium utilizing a pumpless platform for 14 days. Computer simulations of the platform established flow rates and resultant shear stress within accepted ranges. Viability of the system was demonstrated for 14 days as well as functional activity of cardiac, muscle, neuronal and liver modules. The pharmacological relevance of the integrated modules were evaluated for their response at 7 days to 5 drugs with known side effects after a 48 hour drug treatment regime. The results of all drug treatments were in general agreement with published toxicity results from human and animal data. The presented phenotypic culture model exhibits a multi-organ toxicity response, representing the next generation of in vitro systems, and constitutes a step towards an in vitro "human-on-a-chip" assay for systemic toxicity screening.
我们报告了一种功能性人体模型,该模型利用无泵平台在无血清限定培养基中,于连续流动条件下在一个四器官系统中评估多器官毒性,持续14天。该平台的计算机模拟确定了流速以及由此产生的剪应力在可接受范围内。该系统的活力在14天内得到了证明,同时心脏、肌肉、神经元和肝脏模块的功能活性也得到了证明。在48小时的药物治疗方案后,评估了整合模块对5种已知副作用药物在7天时的反应的药理学相关性。所有药物治疗的结果总体上与已发表的来自人类和动物数据的毒性结果一致。所呈现的表型培养模型表现出多器官毒性反应,代表了下一代体外系统,并朝着用于全身毒性筛选的体外“人体芯片”检测迈出了一步。