Institute of Cytology, Russian Academy of Sciences, St. Petersburg, Russia.
PLoS One. 2011;6(11):e27345. doi: 10.1371/journal.pone.0027345. Epub 2011 Nov 4.
The rat represents an important animal model that, in many respects, is superior to the mouse for dissecting behavioral, cardiovascular and other physiological pathologies relevant to humans. Derivation of induced pluripotent stem cells from rats (riPS) opens the opportunity for gene targeting in specific rat strains, as well as for the development of new protocols for the treatment of different degenerative diseases. Here, we report an improved lentivirus-based hit-and-run riPS derivation protocol that makes use of small inhibitors of MEK and GSK3. We demonstrate that the excision of proviruses does not affect either the karyotype or the differentiation ability of these cells. We show that the established riPS cells are readily amenable to genetic manipulations such as stable electroporation. Finally, we propose a genetic tool for an improvement of riPS cell quality in culture. These data may prompt iPS cell-based gene targeting in rat as well as the development of iPS cell-based therapies using disease models established in this species.
大鼠是一种重要的动物模型,在许多方面优于小鼠,可用于剖析与人类相关的行为、心血管和其他生理病理学。从大鼠中诱导多能干细胞(riPS)的出现为特定大鼠品系中的基因靶向以及开发治疗不同退行性疾病的新方案提供了机会。在这里,我们报告了一种改进的基于慢病毒的“打了就跑”riPS 衍生方案,该方案利用 MEK 和 GSK3 的小分子抑制剂。我们证明,前病毒的切除既不影响这些细胞的染色体核型,也不影响其分化能力。我们表明,所建立的 riPS 细胞很容易进行遗传操作,如稳定的电穿孔。最后,我们提出了一种用于提高 riPS 细胞在培养中质量的遗传工具。这些数据可能会促使大鼠中的 iPS 细胞基因靶向以及使用该物种中建立的疾病模型进行 iPS 细胞为基础的治疗。