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人视网膜祖细胞移植片改善严重视网膜变性大鼠的视力。

Sheets of human retinal progenitor transplants improve vision in rats with severe retinal degeneration.

机构信息

Stem Cell Research Center, University of CalifoArnia, Irvine, United States.

Stem Cell Research Center, University of CalifoArnia, Irvine, United States; Department of Physical Medicine & Rehabilitation, University of California, Irvine, United States.

出版信息

Exp Eye Res. 2018 Sep;174:13-28. doi: 10.1016/j.exer.2018.05.017. Epub 2018 May 18.

Abstract

Loss of photoreceptors and other retinal cells is a common endpoint in retinal degenerate (RD) diseases that cause blindness. Retinal transplantation is a potential therapy to replace damaged retinal cells and improve vision. In this study, we examined the development of human fetal retinal sheets with or without their retinal pigment epithelium (RPE) transplanted to immunodeficient retinal degenerate rho S334ter-3 rats. Sheets were dissected from fetal human eyes (11-15.7 weeks gestation) and then transplanted to the subretinal space of 24-31 d old RD nude rats. Every month post surgery, eyes were imaged by high-resolution spectral-domain optical coherence tomography (SD-OCT). SD-OCT showed that transplants were placed into the subretinal space and developed laminated areas or rosettes, with clear development of plexiform layers first seen in OCT at 3 months post surgery. Several months later, as could be expected by the much slower development of human cells compared to rat cells, transplant photoreceptors developed inner and later outer segments. Retinal sections were analyzed by immunohistochemistry for human and retinal markers and confirmed the formation of several retinal subtypes within the retinal layers. Transplant cells extended processes and a lot of the cells could also be seen migrating into the host retina. At 5.8-8.6 months post surgery, selected rats were exposed to light flashes and recorded for visual responses in superior colliculus, (visual center in midbrain). Four of seven rats with transplants showed responses to flashes of light in a limited area of superior colliculus. No response with the same dim light intensity was found in age-matched RD controls (non-surgery or sham surgery). In summary, our data showed that human fetal retinal sheets transplanted to the severely disturbed subretinal space of RD nude rats develop mature photoreceptors and other retinal cells, integrate with the host and induce vision improvement.

摘要

光感受器和其他视网膜细胞的丧失是导致失明的视网膜退行性疾病(RD)的共同终点。视网膜移植是一种潜在的治疗方法,可以替代受损的视网膜细胞并改善视力。在这项研究中,我们研究了在免疫缺陷的 RD 裸鼠 rho S334ter-3 中移植带有或不带有视网膜色素上皮(RPE)的人胎儿视网膜片的发育情况。将视网膜片从 11-15.7 周龄的人胎儿眼睛中分离出来,然后移植到 24-31 天大的 RD 裸鼠的视网膜下腔。手术后每个月,通过高分辨率谱域光学相干断层扫描(SD-OCT)对眼睛进行成像。SD-OCT 显示,移植物被置于视网膜下腔并形成层状区域或玫瑰花结,手术后 3 个月首次在 OCT 上看到了明显的神经丛层发育。几个月后,可以预期与大鼠细胞相比,人类细胞的发育速度要慢得多,移植的光感受器形成了内节和后来的外节。通过免疫组织化学分析视网膜切片,对人源和视网膜标志物进行了分析,并确认在视网膜层内形成了几种视网膜亚型。移植细胞伸出突起,并且可以看到许多细胞也迁移到宿主视网膜中。手术后 5.8-8.6 个月,选择的大鼠暴露于光闪烁并记录中脑上的高级视丘的视觉反应。七只接受移植的大鼠中有四只在高级视丘的有限区域对光闪烁有反应。在年龄匹配的 RD 对照组(未手术或假手术)中,没有发现相同弱光强度的反应。总之,我们的数据表明,移植到 RD 裸鼠严重紊乱的视网膜下腔的人胎儿视网膜片可发育成熟的光感受器和其他视网膜细胞,与宿主整合并诱导视力改善。

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