Institute of Advanced Clinical Medicine, Kinki University School of Medicine, Osaka-Sayama, Osaka, Japan.
Theriogenology. 2010 Jul 1;74(1):135-45. doi: 10.1016/j.theriogenology.2010.01.024. Epub 2010 Mar 7.
Recent studies have illustrated multiple differentiation potentials of embryonic stem cells (ESCs), derived from parthenogenetic embryos, to various kinds of cells (all three embryonic germ layers). However, differentiation diversity of the parthenogenetic ESCs (PgESCs) in vivo remains to be elucidated. In the present study, we established mouse PgESC-lines and observed their contribution diversity in vivo by producing chimeric mice using embryos possessing single nucleotide polymorphisms of mitochondrial DNA (mtDNA) as hosts. Based on southern blot analysis using specific probes to detect the SNPs on mtDNA, PgESC-derived mtDNA were contained in many organs such as brain, lung, and heart of the chimeric mouse. We concluded that PgESCs contributed to various internal organs in vivo, and that they were also stably maintained in adult animals.
最近的研究表明,源于孤雌胚胎的胚胎干细胞 (ESCs) 具有向各种细胞(三个胚胎胚层)分化的多种潜能。然而,孤雌胚胎干细胞 (PgESCs) 在体内的分化多样性仍有待阐明。在本研究中,我们建立了小鼠 PgESC 系,并通过使用具有线粒体 DNA (mtDNA) 单核苷酸多态性的胚胎作为宿主来产生嵌合小鼠,观察了它们在体内的贡献多样性。基于使用特异性探针检测 mtDNA 上 SNPs 的Southern blot 分析,PgESC 衍生的 mtDNA 存在于嵌合小鼠的许多器官中,如脑、肺和心脏。我们得出结论,PgESCs 体内参与各种内部器官的形成,并且在成年动物中也能稳定维持。