Zaehres Holm, Kim Jeong Beom, Schöler Hans R
Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, NRW, Germany.
Methods Enzymol. 2010;476:309-25. doi: 10.1016/S0076-6879(10)76018-3.
Reprogramming of mouse and human somatic cells into induced pluripotent stem (iPS) cells has been possible with retroviral expression of the pluripotency-associated transcription factors Oct4, Sox2, Nanog, and Lin28 as well as Klf4 and c-Myc. iPS cells hold great potential as a model for diseases from the perspective of the individual patient and as an alternative source of pluripotent stem cells for therapeutic applications. In this chapter, we discuss how the use of retroviruses as well as other expression vectors, protein transduction, and small molecules can effectively and efficiently induce pluripotent stem cells from a variety of mouse and human starting somatic cell populations.
通过逆转录病毒表达多能性相关转录因子Oct4、Sox2、Nanog、Lin28以及Klf4和c-Myc,已能够将小鼠和人类体细胞重编程为诱导多能干细胞(iPS细胞)。从个体患者的角度来看,iPS细胞作为疾病模型具有巨大潜力,并且作为治疗应用中多能干细胞的替代来源也具有巨大潜力。在本章中,我们将讨论如何使用逆转录病毒以及其他表达载体、蛋白质转导和小分子,能够从多种小鼠和人类起始体细胞群体中有效且高效地诱导产生多能干细胞。