Section of Gastroenterology, Department of Medicine and Center for Regenerative Medicine (CReM), Boston University School of Medicine, Boston, MA 02118, USA.
Stem Cell Res Ther. 2010 Aug 10;1(3):26. doi: 10.1186/scrt26.
Derivation of autologous induced pluripotent stem cells (iPSCs) through direct reprogramming of easily accessible somatic cells holds the potential to transform the field of regenerative medicine. Since Takahashi and Yamanaka's groundbreaking study describing the generation of iPSCs by retroviral-mediated delivery of defined transcription factors, substantial progress has been made to improve both the efficiency and safety of the method. These advances have provided new insights into the molecular mechanisms of reprogramming and promise to accelerate the clinical translation of iPSC technology. Here, we summarize current reprogramming methodologies with a focus on the production of transgene-free or genetically unmanipulated iPSCs and highlight important technical details that ultimately may influence the biological properties of pluripotent stem cells.
通过直接重编程易于获得的体细胞来衍生自体诱导多能干细胞(iPSCs)有可能彻底改变再生医学领域。自从Takahashi 和 Yamanaka 通过逆转录病毒介导的特定转录因子传递描述了 iPSCs 的产生以来,在提高该方法的效率和安全性方面已经取得了实质性的进展。这些进展为重新编程的分子机制提供了新的见解,并有望加速 iPSC 技术的临床转化。在这里,我们总结了当前的重编程方法,重点是生产无转基因或未经基因改造的 iPSCs,并强调了可能最终影响多能干细胞生物学特性的重要技术细节。