Florey Institute for Neuroscience and Mental Health, Royal Parade, Parkville, Victoria, Australia.
Department of Electrical and Electronic Engineering, Centre for Neural Engineering, University of Melbourne, Royal Parade, Parkville, Victoria, Australia.
Stem Cells Transl Med. 2017 Jun;6(6):1547-1556. doi: 10.1002/sctm.16-0198. Epub 2017 Feb 15.
The capacity for induced pluripotent stem (iPS) cells to be differentiated into a wide range of neural cell types makes them an attractive donor source for autologous neural transplantation therapies aimed at brain repair. Translation to the in vivo setting has been difficult, however, with mixed results in a wide variety of preclinical models of brain injury and limited information on the basic in vivo properties of neural grafts generated from human iPS cells. Here we have generated a human iPS cell line constitutively expressing green fluorescent protein as a basis to identify and characterize grafts resulting from transplantation of neural progenitors into the adult rat brain. The results show that the grafts contain a mix of neural cell types, at various stages of differentiation, including neurons that establish extensive patterns of axonal growth and progressively develop functional properties over the course of 1 year after implantation. These findings form an important basis for the design and interpretation of preclinical studies using human stem cells for functional circuit re-construction in animal models of brain injury. Stem Cells Translational Medicine 2017;6:1547-1556.
诱导多能干细胞(iPS)能够分化为多种神经细胞类型,这使它们成为自体神经移植疗法的有吸引力的供体来源,这种疗法旨在修复大脑。然而,将其转化为体内环境一直具有挑战性,在各种脑损伤的临床前模型中得到的结果喜忧参半,并且关于源自人类 iPS 细胞的神经移植物的基本体内特性的信息有限。在这里,我们生成了一种稳定表达绿色荧光蛋白的人 iPS 细胞系,作为鉴定和表征源自将神经祖细胞移植到成年大鼠脑内的移植物的基础。结果表明,移植物包含多种处于不同分化阶段的神经细胞类型,包括神经元,它们在植入后 1 年内建立了广泛的轴突生长模式,并逐渐发展出功能性特征。这些发现为使用人类干细胞在脑损伤动物模型中进行功能性回路重建的临床前研究的设计和解释奠定了重要基础。Stem Cells Translational Medicine 2017;6:1547-1556.