Efficient generation of retinal progenitor cells from human embryonic stem cells

被引:504
作者
Lamba, Deepak A.
Karl, Mike O.
Ware, Carol B.
Reh, Thomas A. [1 ]
机构
[1] Univ Washington, Dept Biol Struct, Seattle, WA 98195 USA
[2] Univ Washington, Dept Comparat Med, Seattle, WA 98195 USA
[3] Univ Washington, Neurobiol & Behav Program, Seattle, WA 98195 USA
关键词
photoreceptors; eye development; neurogenesis;
D O I
10.1073/pnas.0601990103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The retina is subject to degenerative conditions, leading to blindness. Although retinal regeneration is robust in lower vertebrates, regeneration does not occur in the adult mammalian retina. Thus, we have developed efficient methods for deriving retinal neurons from human embryonic stem (hES) cells. Under appropriate culture conditions, up to 80% of the H1 line can be directed to the retinal progenitor fate, and express a gene expression profile similar to progenitors derived from human fetal retina. The hES cell-derived progenitors differentiate primarily into inner retinal neurons (ganglion and amacrine cells), with functional glutamate receptors. Upon coculture with retinas derived from a mouse model of retinal degeneration, the hES cell derived retinal progenitors integrate with the degenerated mouse retina and increase in their expression of photoreceptor-specific markers. These results demonstrate that human ES cells can be selectively directed to a neural retinal cell fate and thus may be useful in the treatment of retinal degenerations.
引用
收藏
页码:12769 / 12774
页数:6
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