Cui Guanghui, Qi Zhengyu, Zhang Yanmin, Long Xia, Qin Jie, Guo Xin
Guangdong Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Medical Center of Peking University and Hong Kong Science and Technology University, Guangdong, 518036, China.
Cell Biol Int. 2014 Sep;38(9):1069-75. doi: 10.1002/cbin.10305. Epub 2014 May 19.
The adipose stromal vascular fraction (SVF) contains abundant mesenchymal stem cell populations that have a limited ability to self-renew and differentiate. Male mouse adipose SVF cells were dedifferentiated by reprogramming factors (c-Myc, Oct4, Sox2, and Klf4) to form embryonic stem cell-like cells (ESCLCs), which upgraded their limited differentiation potential. The ESCLCs were induced to differentiate toward epiblast-like cells (EpiLCs) and primordial germ cell-like cells (PGCLCs) by culturing in media supplied with activin A and BMP-4, respectively. The derived ESCLCs possess embryonic stem cell features and can automatically form embryonic bodies. After culture in EpiLC induction medium for 2-3 days, ESCLCs formed flattened epithelial structures that were different from their original water drop-like colonies, and the expression of pluripotency-related genes decreased. When the cells that had been cultured in EpiLC induction medium for 2 days were isolated and cultured in PGCLC induction medium for 4-6 days, they formed typical water drop-like colonies again. Moreover, expression of the pluripotency-related genes and the primordial germ cell (PGC) specification-related genes increased. During progression from ESCLCs toward EpiLCs and PGCLCs, the levels of histone methylases H3K9me2 and H3K27me3 kept changing, which resembled those seen in PGC specification. The derived PGCLCs expressed SSEA-1, Blimp-1, and Stella. Furthermore, methylation of Igf2r and Snrpn was retained, but H19 and Kcnq1ot1 methylation levels were slightly reduced compared to non-PGCLCs, suggesting that the derived PGCLCs may have initiated the process of imprint erasure.
脂肪组织的基质血管成分(SVF)包含丰富的间充质干细胞群体,这些细胞自我更新和分化的能力有限。雄性小鼠脂肪SVF细胞通过重编程因子(c-Myc、Oct4、Sox2和Klf4)去分化形成胚胎干细胞样细胞(ESCLCs),从而提升了它们有限的分化潜能。分别在添加激活素A和骨形态发生蛋白4(BMP-4)的培养基中培养,可诱导ESCLCs分化为上胚层样细胞(EpiLCs)和原始生殖细胞样细胞(PGCLCs)。所获得的ESCLCs具有胚胎干细胞特征,并且能够自动形成胚状体。在EpiLC诱导培养基中培养2至3天后,ESCLCs形成了扁平的上皮结构,这与它们原来水滴状的集落不同,并且多能性相关基因的表达下降。当将在EpiLC诱导培养基中培养2天的细胞分离出来并在PGCLC诱导培养基中培养4至6天时,它们又形成了典型的水滴状集落。此外,多能性相关基因和原始生殖细胞(PGC)特化相关基因的表达增加。在从ESCLCs向EpiLCs和PGCLCs的转变过程中,组蛋白甲基转移酶H3K9me2和H3K27me3的水平不断变化,这与PGC特化过程中的情况相似。所获得的PGCLCs表达阶段特异性胚胎抗原-1(SSEA-1)、B淋巴细胞诱导成熟蛋白1(Blimp-1)和干细胞因子(Stella)。此外,胰岛素样生长因子2受体(Igf2r)和小核核糖核蛋白多肽N(Snrpn)的甲基化得以保留,但与非PGCLCs相比,H19和Kcnq1重叠转录本1(Kcnq1ot1)的甲基化水平略有降低,这表明所获得的PGCLCs可能已经启动了印记擦除过程。