Generation of Rx+/Pax6+ neural retinal precursors from embryonic stem cells

被引:247
作者
Ikeda, H
Osakada, F
Watanabe, K
Mizuseki, K
Haraguchi, T
Miyoshi, H
Kamiya, D
Honda, Y
Sasai, N
Yoshimura, N
Takahashi, M
Sasai, Y [1 ]
机构
[1] RIKEN, Ctr Dev Biol, Organogenesis & Neurogenesis Grp, Kobe, Hyogo 6500047, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Ophthalmol & Visual Sci, Kyoto 6068507, Japan
[3] Kyoto Univ, Kyoto Univ Hosp, Translat Res Ctr, Dept Expt Therapeut, Kyoto 6068507, Japan
[4] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Pharmacol, Kyoto 6068507, Japan
[5] RIKEN, BioResource Ctr, Tsukuba, Ibaraki 3050074, Japan
关键词
regenerative medicine; differentiation; photoreceptor; induction; Six3;
D O I
10.1073/pnas.0500010102
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
We report directed differentiaion of retinal precursors in vitro from mouse ES cells. Six3(+) rostral brain progenitors are generated by culturing ES cells under serum-free suspension conditions (SFEB culture) in the presence of Writ and Nodal antagonists (Dkk1 and LeftyA), and subsequently steered to differentiate into Rx(+) cells (16 %) by treatment with activin and serum. Consistent with the characteristics of early neural retinal precursors, the induced Rx+ cells coexpress Pax6 and the mitotic marker Ki67, but not Nestin. The ES cell-derived precursors efficiently generate cells with the photoreceptor phenotype (rhodopsin(+), recoverin(+)) when cocultured with embryonic retinal cells. Furthermore, organotypic culture studies demonstrate the selective integration and survival of ES cell-derived cells with the photoreceptor phenotype (marker expression and morphology) in the outer nuclear layer of the retina. Taken together, ES cells treated with SFEB/Dkk1/LeftyA/ serum/activin generate neural retinal precursors, which have the competence of photoreceptor differentiation.
引用
收藏
页码:11331 / 11336
页数:6
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