State Key Laboratory of Medicinal Chemical Biology, Nankai University, 94 Weijin Road, Tianjin, 300071, China.
Department of Cell Biology and Genetics, Nankai University, 94 Weijin Road, Tianjin, 300071, China.
Nat Commun. 2018 Jul 5;9(1):2620. doi: 10.1038/s41467-018-05038-2.
Feeder cells like mouse embryonic fibroblasts (MEFs) have been widely applied for culture of pluripotent stem cells, but their roles remain elusive. Noticeably, ESCs cultured on the feeders display transcriptional heterogeneity. We investigated roles of feeder cells by examining the telomere maintenance. Here we show that telomere is longer in mESCs cultured with than without the feeders. mESC cultures without MEF feeders exhibit telomere loss, chromosomal fusion, and aneuploidy with increasing passages. Notably, feeders facilitate heterogeneous transcription of 2-cell genes including Zscan4 and telomere elongation. Moreover, feeders produce Fstl1 that together with BMP4 periodically activate Zscan4. Interestingly, Zscan4 is repressed in mESCs cultured in 2i (inhibitors of Mek and Gsk3β signaling) media, associated with shorter telomeres and increased chromosome instability. These data suggest the important role of feeders in maintaining telomeres for long-term stable self-renewal and developmental pluripotency of mESCs.
饲养细胞(如小鼠胚胎成纤维细胞,MEFs)已被广泛应用于多能干细胞的培养,但它们的作用仍不清楚。值得注意的是,在饲养细胞上培养的胚胎干细胞显示出转录异质性。我们通过检测端粒维持来研究饲养细胞的作用。在这里,我们发现与没有饲养细胞的培养相比,mESCs 的端粒更长。在没有 MEF 饲养细胞的 mESC 培养中,随着传代次数的增加,会出现端粒丢失、染色体融合和非整倍体。值得注意的是,饲养细胞促进了包括 Zscan4 和端粒延长在内的 2 细胞基因的异质性转录。此外,饲养细胞产生 Fstl1,与 BMP4 一起周期性地激活 Zscan4。有趣的是,Zscan4 在含有 Mek 和 Gsk3β 信号抑制剂的 2i 培养基中被抑制,与端粒较短和染色体不稳定性增加有关。这些数据表明,饲养细胞在维持 mESCs 的端粒以实现长期稳定的自我更新和发育多能性方面发挥着重要作用。