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药物发现中的原代细胞和干细胞:用于高通量筛选的新兴工具。

Primary cells and stem cells in drug discovery: emerging tools for high-throughput screening.

作者信息

Eglen Richard, Reisine Terry

机构信息

Bio-discovery, PerkinElmer, Waltham, Massachusetts 02451-1457, USA.

出版信息

Assay Drug Dev Technol. 2011 Apr;9(2):108-24. doi: 10.1089/adt.2010.0305. Epub 2010 Dec 27.

DOI:10.1089/adt.2010.0305
PMID:21186936
Abstract

Many drug discovery screening programs employ immortalized cells, recombinantly engineered to express a defined molecular target. Several technologies are now emerging that render it feasible to employ more physiologically, and clinically relevant, cell phenotypes. Consequently, numerous approaches use primary cells, which retain many functions seen in vivo, as well as endogenously expressing the target of interest. Furthermore, stem cells, of either embryonic or adult origin, as well as those derived from differentiated cells, are now finding a place in drug discovery. Collectively, these cells are expanding the utility of authentic human cells, either as screening tools or as therapeutics, as well as providing cells derived directly from patients. Nonetheless, the growing use of phenotypically relevant cells (including primary cells or stem cells) is not without technical difficulties, particularly when their envisioned use lies in high-throughput screening (HTS) protocols. In particular, the limited availability of homogeneous primary or stem cell populations for HTS mandates that novel technologies be developed to accelerate their adoption. These technologies include detection of responses with very few cells as well as protocols to generate cell lines in abundant, homogeneous populations. In parallel, the growing use of changes in cell phenotype as the assay readout is driving greater use of high-throughput imaging techniques in screening. Taken together, the greater availability of novel primary and stem cell phenotypes as well as new detection technologies is heralding a new era of cellular screening. This convergence offers unique opportunities to identify drug candidates for disorders at which few therapeutics are presently available.

摘要

许多药物发现筛选项目采用永生化细胞,通过重组工程使其表达特定的分子靶点。目前正在出现几种技术,使得采用更具生理学和临床相关性的细胞表型成为可行。因此,许多方法使用原代细胞,原代细胞保留了许多在体内可见的功能,并且内源性表达感兴趣的靶点。此外,胚胎来源或成体来源的干细胞,以及那些源自分化细胞的干细胞,现在正在药物发现中占据一席之地。总体而言,这些细胞正在扩大真实人类细胞作为筛选工具或治疗手段的用途,同时也提供直接来源于患者的细胞。然而,越来越多地使用表型相关细胞(包括原代细胞或干细胞)并非没有技术难题,特别是当它们预期用于高通量筛选(HTS)方案时。具体而言,用于HTS的均匀原代或干细胞群体的有限可用性要求开发新技术以加速其应用。这些技术包括用极少细胞检测反应,以及生成大量均匀群体细胞系的方案。与此同时,越来越多地将细胞表型变化用作检测读数,这推动了高通量成像技术在筛选中的更多应用。总之,新型原代和干细胞表型以及新检测技术的更多可用性正在开创细胞筛选的新时代。这种融合为识别目前几乎没有治疗手段的疾病的候选药物提供了独特机会。

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