应用反馈系统控制(FSC)确定最佳成骨药物组合

Y. Honda, Xianting Ding, F. Mussano, Akira Wiberg, Chih-Ming Ho, I. Nishimura
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引用次数: 1

摘要

我们建立了一种新的快速药物筛选方法,反馈系统控制(FSC)与差分进化(DE),以寻找最佳的药物组合,诱导间充质干细胞强大的成骨细胞形成。制备了包括BMP-2在内的7个独立因子组成的10种不同浓度的原型药物鸡尾酒,考察了FSC的效率。作为一项试验,两种成骨生物标志物被用作FSC过程中的适应度指标:碱性磷酸酶(ALP)表达作为早期成骨标志物,体外钙沉淀作为后期标志物。值得注意的是,FSC使用ALP测定鉴定的药物混合物缺乏诱导体外矿化。下一个FSC试验与矿化分析确定了一组不同的药物混合物,产生更具体的成骨分化。在这些药物混合物中,所需的BMP-2剂量差异很大。结果表明,FSC是优化组合药物鸡尾酒的有效工具。此外,鉴定出的多因子可能为阐明成骨分化等复杂的生物系统提供新的线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of feedback system control (FSC) to identify the optimized osteogenic drug cocktails
We established a novel expeditious drug screening approach, Feedback system control (FSC) with differential evolution (DE), to search for optimal drug cocktails that induced robust osteoblastogenesis of mesenchymal stem cells. The prototype drug cocktails composed of 7 independent factors including BMP-2 at 10 different concentrations were prepared to investigate the efficiency of FSC. As a trial, two osteogenic biomarkers were utilized as fitness indices in the FSC processes: alkaline phosphatase (ALP) expression as an early osteogenic marker and in vitro calcium precipitation as a later marker. Notably, drug cocktails that FSC identified using the ALP assay lacked to induce in vitro mineralization. The next FSC trial with mineralization assays identified a different set of drug cocktails that generated more specific osteogenic differentiation. The required doses of BMP-2 varied significantly in these drug cocktails. The results demonstrated the FSC to be a useful tool in optimizing the combinatory drug cocktails. Furthermore, the identified multiple factors may provide a novel clue to elucidate the complex biological system, such as osteogenic differentiation.
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