Xiao Chun, Qian Meilin, Yin Chaoran, Zhang Yonggang, Hu Huozhen, Yao Shaohua
College of life Science and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China.
J Mol Histol. 2016 Oct;47(5):437-44. doi: 10.1007/s10735-016-9688-x. Epub 2016 Aug 23.
The differentiation potentials of stem cells have been evaluated by various in vivo and in vitro assays. However, these assays have different limitations hindering efficient study of mammalian stem cells. Here we describe a rapid and powerful mosaic assay to study the differentiation potentials of stem cells in real time in vivo by using zebrafish embryo. We transplanted mouse neural stem cells into zebrafish embryos at different developmental stages and found that they mainly formed neural tissues while occasionally trans-differentiated into mesoderm- and endoderm-derived tissues. Because zebrafish embryo is transparent, the behaviors of transplanted mouse stem cells can be easily tracked in a real-time manner and at single-cell resolution. We expect that this assay may be widely applied to explore the in vivo behaviors of any stem cells available.
干细胞的分化潜能已通过各种体内和体外试验进行了评估。然而,这些试验存在不同的局限性,阻碍了对哺乳动物干细胞的高效研究。在此,我们描述了一种快速且强大的镶嵌试验,通过使用斑马鱼胚胎在体内实时研究干细胞的分化潜能。我们将小鼠神经干细胞移植到不同发育阶段的斑马鱼胚胎中,发现它们主要形成神经组织,偶尔会转分化为中胚层和内胚层来源的组织。由于斑马鱼胚胎是透明的,移植的小鼠干细胞的行为能够以单细胞分辨率实时轻松追踪。我们期望这种试验可广泛应用于探索任何可用干细胞的体内行为。