Zhang Xue, Xue Binghua, Li Yan, Wei Renyue, Yu Zhuoran, Jin Junxue, Zhang Yu, Liu Zhonghua
Key Laboratory of Animal Cellular and Genetic Engineering of Heilongjiang Province, College of Life Science, Northeast Agricultural University, Harbin, Heilongjiang, China.
J Cell Physiol. 2019 Sep;234(9):15380-15394. doi: 10.1002/jcp.28185. Epub 2019 Jan 30.
Development and improvement of in vitro culture system supporting self-renewal and unlimited proliferation of porcine pluripotent stem cells (pPSCs) is an indispensable process for the naïve pPSCs establishment. In this study, we modified the previous culture system and attempted to develop a novel chemically defined medium (KOFL) for the establishment of pPSCs. It has been cultured >45 passages with flat colony morphology and normal karyotypes in in vitro environment. These cells exhibited alkaline phosphatase activity and expressed pluripotency markers such as OCT4, SOX2, and NANOG, and also possessed differentiation abilities both in vitro and in vivo, proving by the formation of embryonic bodies and teratomas into three germ layers. Then the cells transfected with a green fluorescent protein (GFP) and the GFP positive cells contribute to the porcine preimplantation embryo development. In addition, these cells maintained long duration under feeder-free condition. In conclusion, our results demonstrated that the pPSCs could be derived from preimplantation porcine embryos in serum-free medium and cultured under the feeder-free condition, providing an effective reference for further optimization of the pPSCs culture system.
支持猪多能干细胞(pPSCs)自我更新和无限增殖的体外培养系统的开发与改进,是建立原始态pPSCs不可或缺的过程。在本研究中,我们改进了先前的培养系统,并尝试开发一种用于建立pPSCs的新型化学成分明确的培养基(KOFL)。它在体外环境中已培养超过45代,具有扁平的集落形态和正常的核型。这些细胞表现出碱性磷酸酶活性,表达多能性标志物如OCT4、SOX2和NANOG,并且在体外和体内均具有分化能力,通过形成胚状体和畸胎瘤分化为三个胚层得以证明。然后用绿色荧光蛋白(GFP)转染这些细胞,GFP阳性细胞有助于猪植入前胚胎发育。此外,这些细胞在无饲养层条件下能长时间维持。总之,我们的结果表明,pPSCs可以从无血清培养基中的植入前猪胚胎中获得,并在无饲养层条件下培养,为进一步优化pPSCs培养系统提供了有效的参考。