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人诱导多能干细胞来源的光感受器的产生、纯化和移植。

Generation, purification and transplantation of photoreceptors derived from human induced pluripotent stem cells.

机构信息

Department of Biological Structure, University of Washington, Seattle, Washington, United States of America.

出版信息

PLoS One. 2010 Jan 20;5(1):e8763. doi: 10.1371/journal.pone.0008763.

Abstract

BACKGROUND

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.

CONCLUSIONS

This report provides evidence that enriched populations of human photoreceptors can be derived from iPS cells.

摘要

背景

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45b9/2808350/ea5031d4203e/pone.0008763.g001.jpg

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