Ahn K S, Jeon S-J, Jung J-Y, Kim Y S, Kang J H, Shin S, Choi T, Choi S-J, Chung P, Shim H
Departments of Physiology, Dankook University School of Medicine, Cheonan, Chungnam, Korea.
Cytotherapy. 2008;10(7):759-69. doi: 10.1080/14653240802419286.
To study cell replacement therapy using embryonic stem (ES) cells in mice, avoiding immune rejection and tracing the fate of transplanted cells are important issues. This study was carried out to isolate ES cells ubiquitously expressing enhanced green fluorescent protein (EGFP) and test the survival of these cells in allografts in the cochlea of inbred C57BL/6 mice.
Putative ES cells were isolated from blastocysts collected from C57BL/6-green mice ubiquitously expressing EGFP. Pluripotency of these cells was tested by expression of stem cell markers and in vitro differentiation of the cells into embryoid bodies. Isolated EGFP-transgenic ES cells were injected into the cochlea of deafened inbred C57BL/6 mice, and survival of transplanted cells was identified in histologic sections of the cochlea.
Putative ES cells expressed cellular markers for ES cells, including alkaline phosphatase, Oct-4, Nanog and stage-specific embryonic antigen-1. These cells formed embryoid bodies in suspension cultures. Incorporation of transplanted cells was found at the area of spiral ganglion neurons, auditory nerve fibers reaching the organ of Corti and stria vascularis in the scala media. Grafted cells were also found at the location of inner hair cells underneath the tectorial membrane.
The isolation of ES cells from the EGFP-transgenic mouse and transplantation into allogeneic inbred mice may be a useful means of studying cell therapy with respect to the ubiquitous and stable expression of EGFP and elimination of graft rejection.
为了在小鼠中研究使用胚胎干细胞(ES细胞)进行细胞替代疗法,避免免疫排斥以及追踪移植细胞的命运是重要问题。本研究旨在分离普遍表达增强型绿色荧光蛋白(EGFP)的ES细胞,并检测这些细胞在近交系C57BL/6小鼠耳蜗同种异体移植中的存活情况。
从普遍表达EGFP的C57BL/6-绿色小鼠收集的囊胚中分离假定的ES细胞。通过干细胞标志物的表达以及细胞在体外分化为胚状体来检测这些细胞的多能性。将分离的EGFP转基因ES细胞注射到致聋的近交系C57BL/6小鼠的耳蜗中,并在耳蜗的组织学切片中鉴定移植细胞的存活情况。
假定的ES细胞表达ES细胞的细胞标志物,包括碱性磷酸酶、Oct-4、Nanog和阶段特异性胚胎抗原-1。这些细胞在悬浮培养中形成胚状体。在螺旋神经节神经元区域、到达柯蒂氏器的听神经纤维以及中阶的血管纹中发现了移植细胞的掺入。在盖膜下方的内毛细胞位置也发现了移植细胞。
从EGFP转基因小鼠分离ES细胞并移植到同种异体近交系小鼠中,对于EGFP的普遍稳定表达以及消除移植排斥而言,可能是研究细胞治疗的一种有用方法。