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大鼠胚胎干细胞源性视网膜细胞移植可恢复皇家外科学院大鼠的视觉功能。

Transplantation of rat embryonic stem cell-derived retinal cells restores visual function in the Royal College of Surgeons rats.

作者信息

Wu Hongxi, Li Jia, Mao Xinbang, Li Guodong, Xie Lin, You Zhipeng

机构信息

Department of Ophthalmology, The Second Affiliated Hospital of Nanchang University, 1 Minde Road, Nanchang, 330000, China.

出版信息

Doc Ophthalmol. 2018 Oct;137(2):71-78. doi: 10.1007/s10633-018-9648-8. Epub 2018 Aug 3.

Abstract

AIM OF STUDY

To evaluate the feasibility of transplantation of embryonic stem cell (ESC)-derived retinal cells in the treatment of retinal degeneration.

MATERIALS AND METHODS

Rat ESCs were isolated and induced into retinal progenitor cells (RPCs) in vitro, which were subsequently induced into retinal pigment epithelium cells (RPEs) and photoreceptors (PRCs). All cells were identified by Western blot detection of their specific markers. RPEs and PRCs were, respectively, injected into the retina of Royal College of Surgeons (RCSs) rats. Control group was injected with PBS. Post-transplantation visual function was determined by electroretinography (ERG). The histology of the whole eye was compared by H&E staining.

RESULTS

RPEs and PRCs were successfully derived from rat ESCs through the two-step differentiation as indicated by the presence of ESC- (Oct-3/4, Nanog, TRA-1-60 and TRA-1-81), RPC- (Rx, Mitf, Pax6 and Chx10), RPE- (RPE65 and keratin) and PRC-specific markers (blue opsin, red/green opsin, recoverin and rhodopsin) in Western blot. The amplitude of ERG a- and b-wave in RPE- and PRC-transplanted groups at week 2 and 10 after transplantation was markedly higher compared with PBS controls. Retinal injury and vascular stress response was not detected in any of the RCS rats after transplantation.

CONCLUSION

The developed stepwise protocol can derive retinal cells from ESCs. Transplantation of these retinal cells can restore visual function of RCS rats. Our study provides evidence for potential clinical application of ESC-based cell therapy for retinal degeneration.

摘要

研究目的

评估胚胎干细胞(ESC)来源的视网膜细胞移植治疗视网膜变性的可行性。

材料与方法

分离大鼠胚胎干细胞并在体外诱导为视网膜祖细胞(RPC),随后将其诱导为视网膜色素上皮细胞(RPE)和光感受器(PRC)。通过蛋白质免疫印迹法检测所有细胞的特异性标志物进行鉴定。将RPE和PRC分别注射到皇家外科学院(RCS)大鼠的视网膜中。对照组注射磷酸盐缓冲液(PBS)。移植后通过视网膜电图(ERG)测定视觉功能。通过苏木精-伊红(H&E)染色比较全眼的组织学情况。

结果

蛋白质免疫印迹显示,通过两步分化成功从大鼠胚胎干细胞中获得了RPE和PRC,其存在ESC特异性标志物(Oct-3/4、Nanog、TRA-1-60和TRA-1-81)、RPC特异性标志物(Rx、Mitf、Pax6和Chx10)、RPE特异性标志物(RPE65和角蛋白)以及PRC特异性标志物(蓝色视蛋白、红/绿色视蛋白、恢复蛋白和视紫红质)。移植后第2周和第10周,RPE和PRC移植组的ERG a波和b波振幅明显高于PBS对照组。移植后在任何一只RCS大鼠中均未检测到视网膜损伤和血管应激反应。

结论

所建立的分步方案可从胚胎干细胞中获得视网膜细胞。这些视网膜细胞的移植可恢复RCS大鼠的视觉功能。我们的研究为基于胚胎干细胞的细胞疗法治疗视网膜变性的潜在临床应用提供了证据。

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