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首页> 外文期刊>Methods: A Companion to Methods in Enzymology >A high-content imaging-based screening pipeline for the systematic identification of anti-progeroid compounds
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A high-content imaging-based screening pipeline for the systematic identification of anti-progeroid compounds

机译:基于高含量成像的筛选管线,用于系统识别抗早老化合物

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Hutchinson-Gilford Progeria Syndrome (HGPS) is an early onset lethal premature aging disorder caused by constitutive production of progerin, a mutant form of the nuclear architectural protein lamin A. The presence of progerin causes extensive morphological, epigenetic and DNA damage related nuclear defects that ultimately disrupt tissue and organismal functions. Hypothesis-driven approaches focused on HGPS affected pathways have been used in attempts to identify druggable targets with anti-progeroid effects. Here, we report an unbiased discovery approach to HGPS by implementation of a high-throughput, high-content imaging based screening method that enables systematic identification of small molecules that prevent the formation of multiple progerin-induced aging defects. Screening a library of 2816 FDA approved drugs, we identified retinoids as a novel class of compounds that reverses aging defects in HGPS patient skin fibroblasts. These findings establish a novel approach to anti-progeroid drug discovery. (C) 2016 Published by Elsevier Inc.
机译:Hutchinson-Gilford早衰综合症(HGPS)是由构成基因progerin(核建筑蛋白lamin A的突变体)的组成型产生的早期致死性早衰综合症。progerin的存在引起广泛的形态,表观遗传和DNA损伤相关的核缺陷最终破坏组织和机体功能。假说驱动的方法侧重于受HGPS影响的途径,已被用于尝试鉴定具有抗早孕作用的可药物治疗靶标。在这里,我们通过实施高通量,基于高含量成像的筛选方法,报告了一种无偏见的HGPS发现方法,该方法可对小分子进行系统识别,从而防止形成多种由早老蛋白引起的衰老缺陷。通过筛选2816种FDA批准药物的库,我们确定类维生素A是一类新型化合物,可逆转HGPS患者皮肤成纤维细胞中的衰老缺陷。这些发现建立了抗早孕药物发现的新方法。 (C)2016由Elsevier Inc.发布

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