Ji Pengfei, Manupipatpong Sasicha, Xie Nina, Li Yujing
Institute of Genetics and Development Biology, Chinese Academy of Sciences, Beijing 100101, China.
Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Atlanta, GA 30322, USA.
Stem Cells Int. 2016;2016:8415010. doi: 10.1155/2016/8415010. Epub 2016 Jan 5.
Possessing the ability of self-renewal with immortalization and potential for differentiation into different cell types, stem cells, particularly embryonic stem cells (ESC), have attracted significant attention since their discovery. As ESC research has played an essential role in developing our understanding of the mechanisms underlying reproduction, development, and cell (de)differentiation, significant efforts have been made in the biomedical study of ESC in recent decades. However, such studies of ESC have been hampered by the ethical issues and technological challenges surrounding them, therefore dramatically inhibiting the potential applications of ESC in basic biomedical studies and clinical medicine. Induced pluripotent stem cells (iPSCs), generated from the reprogrammed somatic cells, share similar characteristics including but not limited to the morphology and growth of ESC, self-renewal, and potential differentiation into various cell types. The discovery of the iPSC, unhindered by the aforementioned limitations of ESC, introduces a viable alternative to ESC. More importantly, the applications of iPSC in the development of disease models such as neurodegenerative disorders greatly enhance our understanding of the pathogenesis of such diseases and also facilitate the development of clinical therapeutic strategies using iPSC generated from patient somatic cells to avoid an immune rejection. In this review, we highlight the advances in iPSCs generation methods as well as the mechanisms behind their reprogramming. We also discuss future perspectives for the development of iPSC generation methods with higher efficiency and safety.
干细胞具有自我更新、永生化的能力以及分化为不同细胞类型的潜力,自发现以来就备受关注,尤其是胚胎干细胞(ESC)。由于ESC研究在增进我们对生殖、发育和细胞(去)分化机制的理解方面发挥了重要作用,近几十年来,人们在ESC的生物医学研究方面付出了巨大努力。然而,ESC的此类研究受到围绕它们的伦理问题和技术挑战的阻碍,因此极大地抑制了ESC在基础生物医学研究和临床医学中的潜在应用。诱导多能干细胞(iPSC)由重编程的体细胞产生,具有与ESC相似的特征,包括但不限于ESC的形态和生长、自我更新以及分化为各种细胞类型的潜力。iPSC的发现不受ESC上述局限性的限制,为ESC提供了一种可行的替代方案。更重要的是,iPSC在神经退行性疾病等疾病模型开发中的应用极大地增进了我们对这类疾病发病机制的理解,也促进了利用患者体细胞产生的iPSC来避免免疫排斥的临床治疗策略的发展。在这篇综述中,我们重点介绍了iPSC生成方法的进展及其重编程背后的机制。我们还讨论了开发更高效率和安全性的iPSC生成方法的未来前景。