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利用脂肪来源干细胞进行高通量筛选以鉴定脂肪生成调节剂。

Use of adipose-derived stem cells in high-throughput screening to identify modulators of lipogenesis.

作者信息

Lea-Currie Y Reneé, Duffin David J, Buehrer Benjamin M

机构信息

ZenBio, Inc., Research Triangle Park, NC, USA.

出版信息

Methods Mol Biol. 2011;702:359-68. doi: 10.1007/978-1-61737-960-4_26.

Abstract

Drug discovery efforts have an increasing focus on functional cell-based screening to identify compounds that modulate targets presented in a relevant format. Historically, immortalized cell lines have been used in primary and secondary screens due to their ease of manipulation, transformation, and propagation. However, more researchers are using primary cells that present their drug targets in their natural context. Human primary cell isolation and propagation procedures have become efficient enough to provide these cells in the necessary scale for early stage drug discovery. Adult human stem cells provide an opportunity for investigating multiple pathways of differentiation, development, regeneration, and toxicity using a single cell source and type. Adipose-derived stem cells (ASCs) are an attractive adult human primary stem cell for drug discovery due their abundance in adipose tissue, ease of isolation, and propagation in culture. They can be expanded in high numbers and retain their unique properties to differentiate into multiple lineages. In this chapter, we describe a protocol to identify modulators of human ASC lipogenesis following partial differentiation to adipocytes.

摘要

药物研发工作越来越注重基于功能细胞的筛选,以识别能够调节以相关形式呈现的靶点的化合物。从历史上看,永生化细胞系因其易于操作、转化和增殖而被用于初次和二次筛选。然而,越来越多的研究人员正在使用能在自然环境中呈现其药物靶点的原代细胞。人类原代细胞的分离和培养程序已经足够高效,能够为早期药物研发提供所需规模的这些细胞。成人人类干细胞提供了一个机会,可使用单一细胞来源和类型来研究分化、发育、再生和毒性的多种途径。脂肪来源干细胞(ASC)因其在脂肪组织中含量丰富、易于分离且能在培养中增殖,是药物研发中一种有吸引力的成人人类原代干细胞。它们可以大量扩增,并保留其分化为多种谱系的独特特性。在本章中,我们描述了一种在部分分化为脂肪细胞后鉴定人类ASC脂肪生成调节剂的方案。

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