Department of Cell and Developmental Biology, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
Department of Cell and Developmental Biology, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan; JST, CREST, Chiyoda-ku, Tokyo 102-0075, Japan.
Stem Cell Reports. 2015 Oct 13;5(4):480-9. doi: 10.1016/j.stemcr.2015.09.001. Epub 2015 Oct 1.
The role of secreted molecules in cellular reprogramming has been poorly understood. Here we identify a truncated form of ephrin receptor A7 (EPHA7) as a key regulator of reprogramming. Truncated EPHA7 is prominently upregulated and secreted during reprogramming. EPHA7 expression is directly regulated by OCT3/4. EphA7 knockdown results in marked reduction of reprogramming efficiency, and the addition of truncated EPHA7 is able to restore it. ERK activity is markedly reduced during reprogramming, and the secreted, truncated EPHA7 is responsible for ERK activity reduction. Remarkably, treatment of EphA7-knockdown MEFs with the ERK pathway inhibitor restores reprogramming efficiency. Analyses show that truncated EPHA7-induced ERK activity reduction plays an important role in the middle phase of reprogramming. Thus, our findings uncover the importance of secreted EPHA7-induced ERK activity reduction in reprogramming.
细胞重编程过程中分泌分子的作用一直未被很好地理解。在这里,我们发现一种截断形式的 Ephrin 受体 A7(EPHA7)是重编程的关键调节因子。在重编程过程中,截断的 EphA7 明显上调并分泌。EphA7 的表达受 OCT3/4 直接调控。EphA7 敲低导致重编程效率显著降低,而添加截断的 EphA7 能够恢复它。在重编程过程中,ERK 活性明显降低,而分泌的截断 EphA7 负责 ERK 活性的降低。值得注意的是,用 ERK 通路抑制剂处理 EphA7 敲低的 MEFs 可恢复重编程效率。分析表明,截断 EphA7 诱导的 ERK 活性降低在重编程的中期阶段发挥重要作用。因此,我们的研究结果揭示了分泌 EphA7 诱导的 ERK 活性降低在重编程中的重要性。