Kuang Yina, Walt David R
Department of Chemistry, Tufts University, Medford, MA 02155, USA.
Anal Biochem. 2005 Oct 15;345(2):320-5. doi: 10.1016/j.ab.2005.06.028.
Recent advances in genomics and molecular pathogenesis studies have determined that many diseases are caused by a multiplicity of factors. New drug regimens may consist of multiple biologically active agents designed to act synergistically on multiple biochemical targets. Live cell assays are becoming a standard for identifying new drug candidates with an emphasis on "homogeneous" living cell assays in which multiple cell lines are mixed and monitored simultaneously. In this study, we used a high-density single living cell array, based on an optical imaging fiber bundle microwell array, to simultaneously monitor "promiscuous" drug effects on single cells of multiple cell types. Such a capability allows for a more comprehensive understanding of how cells dynamically respond to combinatorial drug libraries or how different cellular pathways and regulation circuits respond cooperatively to drugs in individual cells.
基因组学和分子发病机制研究的最新进展已确定,许多疾病是由多种因素引起的。新的药物方案可能由多种生物活性剂组成,这些活性剂旨在对多个生化靶点产生协同作用。活细胞检测正成为鉴定新候选药物的标准,重点是“均相”活细胞检测,即多种细胞系混合并同时进行监测。在本研究中,我们使用了一种基于光学成像纤维束微孔阵列的高密度单活细胞阵列,以同时监测“混杂”药物对多种细胞类型的单细胞的作用。这种能力有助于更全面地了解细胞如何动态响应组合药物库,或者不同的细胞途径和调节回路如何在单个细胞中协同响应药物。