Department of Biological Structure, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2010 Jan 20;5(1):e8763. doi: 10.1371/journal.pone.0008763.
Inherited and acquired retinal degenerations are frequent causes of visual impairment and photoreceptor cell replacement therapy may restore visual function to these individuals. To provide a source of new retinal neurons for cell based therapies, we developed methods to derive retinal progenitors from human ES cells.
METHODOLOGY/PHYSICAL FINDINGS: In this report we have used a similar method to direct induced pluripotent stem cells (iPS) from human fibroblasts to a retinal progenitor fate, competent to generate photoreceptors. We also found we could purify the photoreceptors derived from the iPS cells using fluorescence activated cell sorting (FACS) after labeling photoreceptors with a lentivirus driving GFP from the IRBP cis-regulatory sequences. Moreover, we found that when we transplanted the FACS purified iPSC derived photoreceptors, they were able to integrate into a normal mouse retina and express photoreceptor markers.
This report provides evidence that enriched populations of human photoreceptors can be derived from iPS cells.
遗传性和获得性视网膜变性是视力损害的常见原因,而光感受器细胞替代疗法可能恢复这些患者的视觉功能。为了为基于细胞的治疗提供新的视网膜神经元来源,我们开发了从人胚胎干细胞中获得视网膜祖细胞的方法。
方法/物理发现:在本报告中,我们使用类似的方法将人成纤维细胞中的诱导多能干细胞(iPS)诱导为视网膜祖细胞命运,有能力生成光感受器。我们还发现,我们可以使用荧光激活细胞分选(FACS)对源自 iPS 细胞的光感受器进行纯化,方法是使用携带 IRBP 顺式调控序列 GFP 的慢病毒对光感受器进行标记。此外,我们发现当我们移植经 FACS 纯化的 iPSC 衍生的光感受器时,它们能够整合到正常的小鼠视网膜中并表达光感受器标记物。
本报告提供了证据表明,人光感受器的富集群体可以从 iPS 细胞中获得。