Institute of Medical Biology and Agency for Science Technology and Research (A*STAR), Singapore, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University-Imperial College London, Singapore, Singapore.
Stem Cells Dev. 2019 Oct 15;28(20):1347-1364. doi: 10.1089/scd.2018.0246. Epub 2019 Sep 18.
The ability of human stem cells to generate somatic cell lineages makes them ideal candidates for use in toxicological testing and eventually, preclinical drug development. Such resources would support an evolution away from human primary cells or research animal models, which suffer from variability and poor predictability, toward off-the-shelf assays of chemical toxicity and drug efficacy using human cells and tissues. To this end, we generated vascular cell populations (smooth muscle cells and endothelial cells) from human pluripotent stem cells (hPSCs), arranged them into 3D co-cultures within supportive gel matrices, and directed their propensity for self-organization resembling microvasculature. The resulting vascular cell populations and co-cultured constructs were then arrayed in high throughput and used for screening a library of environmental and clinical chemical agents for immunological and toxicological responses. The screen effectively stratified the chemicals into various levels of toxicity, with both cell type-specific and co-culture-dependent responses observed. Thus, hPSC-derived vascular cells and constructs could be progressed further toward use in toxicant and drug screening.
人类干细胞生成体细胞谱系的能力使它们成为毒理学测试的理想候选者,并最终成为临床前药物开发的候选者。这些资源将支持从人类原代细胞或研究动物模型中发展,这些模型存在变异性和较差的可预测性,转而使用现成的基于人类细胞和组织的化学毒性和药物功效的检测。为此,我们从人多能干细胞(hPSCs)中生成血管细胞群体(平滑肌细胞和内皮细胞),将它们排列在支持性凝胶基质中的 3D 共培养物中,并指导它们类似于微血管的自组织倾向。然后将得到的血管细胞群体和共培养物构建体进行高通量排列,并用于筛选环境和临床化学试剂文库,以检测免疫和毒性反应。该筛选有效地将化学物质分为不同的毒性水平,观察到了细胞类型特异性和共培养依赖性反应。因此,hPSC 衍生的血管细胞和构建体可以进一步用于筛选毒物和药物。