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首页> 外文期刊>Stem cell research >In vitro culture and characterization of putative porcine embryonic germ cells derived from domestic breeds and Yucatan mini pig embryos at Days 20–24 of gestation - ScienceDirect
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In vitro culture and characterization of putative porcine embryonic germ cells derived from domestic breeds and Yucatan mini pig embryos at Days 20–24 of gestation - ScienceDirect

机译:妊娠第20-24天来自家种和尤卡坦小型猪胚胎的推定猪胚胎生殖细胞的体外培养和鉴定-ScienceDirect

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Embryonic germ cells (EGC) are cultured pluripotent cells derived from primordial germ cells (PGC). This study explored the possibility of establishing porcine EGC from domestic breeds and Yucatan mini pigs using embryos at Days 17–24 of gestation. In vitro culture of PGC from both pooled and individual embryos resulted in the successful derivation of putative EGC lines from Days 20 to 24 with high efficiency. RT-PCR showed that gene expression among all 31 obtained cell lines was very similar, and only minor changes were detected during in vitro passaging of the cells. Genome-wide RNA-Seq expression profiling showed no expression of the core pluripotency markers OCT4, SOX2, and NANOG, although most other pluripotency genes were expressed at levels comparable to those of mouse embryonic stem cells (ESC). Moreover, germ-specific genes such as BLIMP1 retained their expression. Functional annotation clustering of the gene expression pattern of the putative EGC suggests partial differentiation toward endo/mesodermal lineages. The putative EGC were able to form embryoid bodies in suspension culture and to differentiate into epithelial-like, mesenchymal-like, and neuronal-like cells. However, their injection into immunodeficient mice did not result in teratoma formation. Our results suggest that the PGC-derived cells described in this study are EGC-like, but seem to be multipotent rather than pluripotent cells. Nevertheless, the thorough characterization of these cells in this study, and especially the identification of various genes and pathways involved in pluripotency by RNA-Seq, will serve as a rich resource for further derivation of porcine EGC.
机译:胚胎生殖细胞(EGC)是源自原始生殖细胞(PGC)的培养多能细胞。这项研究探讨了在妊娠第17-24天使用胚胎从国内品种和尤卡坦小型猪中建立猪EGC的可能性。从合并的胚胎和单个胚胎进行PGC的体外培养导致成功地从第20天到第24天成功推导了推定的EGC系。 RT-PCR显示在所有31种获得的细胞系中的基因表达非常相似,并且在细胞的体外传代过程中仅检测到很小的变化。全基因组的RNA-Seq表达谱显示核心多能性标记OCT4,SOX2和NANOG没有表达,尽管大多数其他多能性基因的表达水平与小鼠胚胎干细胞(ESC)相当。此外,细菌特异性基因(例如BLIMP1)保留了它们的表达。推定的EGC的基因表达模式的功能注释聚类表明朝着内胚层/中胚层谱系的部分分化。推定的EGC能够在悬浮培养中形成胚状体,并分化为上皮样,间充质样和神经元样细胞。但是,将它们注射到免疫缺陷小鼠中并不会导致畸胎瘤的形成。我们的结果表明,本研究中描述的PGC来源的细胞类似于EGC,但似乎是多能而不是多能的细胞。尽管如此,本研究中这些细胞的全面表征,尤其是RNA-Seq对涉及多能性的各种基因和途径的鉴定,将为进一步衍生猪EGC提供丰富的资源。

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