Laboratory of Receptor-based Bio-medicine, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Acta Pharmacol Sin. 2013 Jun;34(6):765-76. doi: 10.1038/aps.2013.21. Epub 2013 Apr 22.
The revolutionary induced pluripotent stem cell (iPSC) technology provides a new path for cell replacement therapies and drug screening. Patient-specific iPSCs and subsequent differentiated cells manifesting disease phenotypes will finally position human disease pathology at the core of drug discovery. Cells used to test the toxic effects of drugs can also be generated from normal iPSCs and provide a much more accurate and cost-effective system than many animal models. Here, we highlight the recent progress in iPSC-based cell therapy, disease modeling and drug evaluations. In addition, we discuss the use of small molecule drugs to improve the generation of iPSCs and understand the reprogramming mechanism. It is foreseeable that the interplay between iPSC technology and small molecule compounds will push forward the applications of iPSC-based therapy and screening systems in the real world and eventually revolutionize the methods used to treat diseases.
革命性的诱导多能干细胞 (iPSC) 技术为细胞替代疗法和药物筛选提供了新途径。患者特异性 iPSCs 和随后表现出疾病表型的分化细胞将最终使人类疾病病理学处于药物发现的核心位置。用于测试药物毒性影响的细胞也可以从正常 iPSCs 中产生,并提供比许多动物模型更准确和更具成本效益的系统。在这里,我们重点介绍了基于 iPSC 的细胞治疗、疾病建模和药物评估的最新进展。此外,我们还讨论了使用小分子药物来改善 iPSC 的生成以及理解重编程机制。可以预见,iPSC 技术和小分子化合物之间的相互作用将推动基于 iPSC 的治疗和筛选系统在现实世界中的应用,并最终彻底改变治疗疾病的方法。