Pitrez P R, Rosa S C, Praça C, Ferreira L
CNC-Center for Neurosciences and Cell Biology, University of Coimbra, Coimbra, Portugal; Centre of Biological Engineering, University of Minho, Campus de Gualtar, Braga, Portugal.
CNC-Center for Neurosciences and Cell Biology, University of Coimbra, Coimbra, Portugal.
Biochem Biophys Res Commun. 2016 May 6;473(3):710-8. doi: 10.1016/j.bbrc.2015.10.014. Epub 2015 Oct 20.
Induced pluripotent stem cells (iPSCs) represent today an invaluable tool to create disease cell models for modeling and drug screening. Several lines of iPSCs have been generated in the last 7 years that changed the paradigm for studying diseases and the discovery of new drugs to treat them. In this article we focus our attention to vascular diseases in particular Hutchinson-Gilford Progeria Syndrome (HGPS), a devastating premature aging disease caused by a mutation in the lamin A gene. In general, patients die because of myocardial infarction or stroke. Because the patients are fragile the isolation of a particular type of cells is very difficult. Therefore in the last 5 years, researchers have used cells derived from iPSCs to model aspects of the HGPS and to screen libraries of chemicals to retard or treat the disease.
诱导多能干细胞(iPSC)如今是创建用于疾病建模和药物筛选的疾病细胞模型的宝贵工具。在过去7年中已生成了多株iPSC,这改变了疾病研究和治疗疾病新药发现的模式。在本文中,我们将注意力集中于血管疾病,特别是哈钦森 - 吉尔福德早衰综合征(HGPS),这是一种由核纤层蛋白A基因突变引起的毁灭性早衰疾病。一般来说,患者死于心肌梗死或中风。由于患者身体脆弱,分离特定类型的细胞非常困难。因此,在过去5年中,研究人员利用源自iPSC的细胞对HGPS的各个方面进行建模,并筛选化学物质库以延缓或治疗该疾病。