Sugie Yuko, Yoshikawa Masahide, Ouji Yukiteru, Saito Ko, Moriya Kei, Ishizaka Shigeaki, Matsuura Toyoaki, Maruoka Shinji, Nawa Yoshiaki, Hara Yoshiaki
Department of Ophthalmology, Nara Medical University, Nara, Kashihara-Shi 630-8522, Japan.
Biochem Biophys Res Commun. 2005 Jun 24;332(1):241-7. doi: 10.1016/j.bbrc.2005.04.125.
Degeneration of photoreceptors is a consistent and common endpoint in retinal diseases. Herein, we report the efficient induction of photoreceptor-like cells from mouse embryonic stem (ES) cells using chick embryonic retina tissue. Undifferentiated mouse ES cells were initially cultured in a preferential condition into a neural lineage, and ES cells were then co-cultured with chick embryonic day 6 (E6) retina tissues. After a 10-day co-culture, approximately 20% of the mouse ES derivatives became immuno-positive for rhodopsin. RT-PCR analysis demonstrated expression of the transcription factor crx and a distinct increase of rod photoreceptor-specific markers, IRBP and recoverin, after the start of the co-culture. These results indicate that co-culture of ES cells with chick embryonic retina tissue is a useful and efficient method for the induction of photoreceptor-like cells.
光感受器的退化是视网膜疾病中一个一致且常见的终点。在此,我们报告了利用鸡胚视网膜组织从小鼠胚胎干细胞(ES细胞)高效诱导出光感受器样细胞。未分化的小鼠ES细胞最初在优先条件下培养成神经谱系,然后将ES细胞与鸡胚第6天(E6)的视网膜组织共培养。共培养10天后,约20%的小鼠ES细胞衍生物对视紫红质呈免疫阳性。RT-PCR分析表明,共培养开始后,转录因子crx表达,视杆光感受器特异性标志物IRBP和恢复蛋白明显增加。这些结果表明,ES细胞与鸡胚视网膜组织共培养是诱导光感受器样细胞的一种有用且高效的方法。