CAS Key Laboratory of Receptor Research, The National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China; Shanghai Key Laboratory of Signaling and Disease Research, Laboratory of Receptor-based Bio-medicine, School of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Shanghai Key Laboratory of Signaling and Disease Research, Laboratory of Receptor-based Bio-medicine, School of Life Sciences and Technology, Tongji University, Shanghai 200092, China.
Curr Opin Genet Dev. 2017 Oct;46:104-113. doi: 10.1016/j.gde.2017.07.003. Epub 2017 Jul 26.
The revolutionizing somatic cell reprogramming/transdifferentiation technologies provide a new path for cell replacement therapies and drug screening. The original method for reprogramming involves the delivery of exogenous transcription factors, leading to the safety concerns about the possible genome integration. Many efforts have been taken to avoid genetic alteration in somatic cell reprogramming/transdifferentiation by using non-integrating gene delivery approaches, cell membrane permeable proteins, and small molecule compounds. Compared to other methods, small-molecule compounds have several unique advantages, such as structural versatility and being easy to control in a time-dependent and concentration-dependent way. More importantly, small molecules have been used as drugs to treat human diseases for thousands of years. So the small molecule approach to reprogramming might be more acceptable in clinical-related uses. In the past few years, small molecule approaches have made significant progresses in inducing pluripotent or functional differentiated cells from somatic cells. Here we review the recent achievements of chemical reprogramming/transdifferentiation and discuss the advantages and challenges facing this strategy in future applications.
体细胞重编程/转分化技术的革命性进展为细胞替代疗法和药物筛选提供了新途径。最初的重编程方法涉及外源性转录因子的传递,这导致了对可能的基因组整合的安全担忧。为了避免体细胞重编程/转分化中的遗传改变,人们已经采取了许多努力,例如使用非整合基因传递方法、细胞膜可渗透蛋白和小分子化合物。与其他方法相比,小分子化合物具有几个独特的优势,例如结构多样性和易于在时间和浓度依赖性方面进行控制。更重要的是,小分子化合物已经被用作治疗人类疾病的药物数千年。因此,小分子方法在临床相关用途中可能更容易被接受。在过去的几年中,小分子方法在诱导多能性或功能性分化细胞方面取得了重大进展。在这里,我们综述了化学重编程/转分化的最新成果,并讨论了该策略在未来应用中面临的优势和挑战。