Rippon Helen J, Lane Síle, Qin Mingde, Ismail N-Siti, Wilson Michael R, Takata Masao, Bishop Anne E
Section on Experimental Medicine & Toxicology, Faculty of Medicine, Imperial College London, Hammersmith Hospital, Du Cane Road, London, W12 0NN, UK.
Proc Am Thorac Soc. 2008 Aug 15;5(6):717-22. doi: 10.1513/pats.200801-008AW.
Embryonic stem cells (ESCs) derived from the preimplantation blastocyst are pluripotent and capable of indefinite expansion in vitro. As such, they present a cell source to derive a potentially inexhaustible supply of pulmonary cells and tissue. ESC-derived pulmonary epithelium could be used for in vitro cell or tissue models or, in the future, implanted into the damaged or diseased lung to effect repair. Efforts to date have largely focused on obtaining distal lung epithelial phenotypes from ESCs, notably alveolar epithelium. Several disparate methods have been developed to enhance differentiation of ESCs into pulmonary epithelial lineages; these are broadly based on recapitulating developmental signaling events, mimicking the physical environment, or forcibly reprogramming the ESC nucleus. Early findings of our preclinical experiments implanting differentiated ESCs into the injured lung are also described here. Future efforts will focus on maximizing ESC differentiation efficiency and yield of the target phenotype, as well as characterizing the function of derived cells in vivo and in vitro.
源自植入前囊胚的胚胎干细胞(ESC)具有多能性,能够在体外无限扩增。因此,它们提供了一种细胞来源,可用于获取潜在的无穷无尽的肺细胞和组织供应。ESC衍生的肺上皮细胞可用于体外细胞或组织模型,或者在未来植入受损或患病的肺部以实现修复。迄今为止的努力主要集中于从ESC获得远端肺上皮表型,尤其是肺泡上皮。已经开发了几种不同的方法来增强ESC向肺上皮谱系的分化;这些方法主要基于重现发育信号事件、模拟物理环境或强行重编程ESC细胞核。本文还描述了我们将分化的ESC植入受损肺部的临床前实验的早期发现。未来的努力将集中于最大化ESC分化效率和目标表型的产量,以及表征衍生细胞在体内和体外的功能。