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免疫缺陷型视网膜变性模型小鼠的建立及人 ESC 衍生视网膜片移植后的功能成熟。

Establishment of Immunodeficient Retinal Degeneration Model Mice and Functional Maturation of Human ESC-Derived Retinal Sheets after Transplantation.

机构信息

Laboratory for Retinal Regeneration, Center for Developmental Biology, RIKEN, Kobe, Hyogo 650-0047, Japan; Department of Ophthalmology, Faculty of Life Sciences, Kumamoto University, Kumamoto 860-8556, Japan; Application Biology and Regenerative Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan.

Laboratory for Retinal Regeneration, Center for Developmental Biology, RIKEN, Kobe, Hyogo 650-0047, Japan.

出版信息

Stem Cell Reports. 2018 Mar 13;10(3):1059-1074. doi: 10.1016/j.stemcr.2018.01.032. Epub 2018 Mar 1.

Abstract

Increasing demand for clinical retinal degeneration therapies featuring human ESC/iPSC-derived retinal tissue and cells warrants proof-of-concept studies. Here, we established two mouse models of end-stage retinal degeneration with immunodeficiency, NOG-rd1-2J and NOG-rd10, and characterized disease progress and immunodeficient status. We also transplanted human ESC-derived retinal sheets into NOG-rd1-2J and confirmed their long-term survival and maturation of the structured graft photoreceptor layer, without rejection or tumorigenesis. We recorded light responses from the host ganglion cells using a multi-electrode array system; this result was consistent with whole-mount immunostaining suggestive of host-graft synapse formation at the responding sites. This study demonstrates an application of our mouse models and provides a proof of concept for the clinical use of human ESC-derived retinal sheets.

摘要

为满足对以人 ESC/iPSC 衍生的视网膜组织和细胞为特色的临床视网膜变性疗法的需求,需要进行概念验证研究。在这里,我们建立了两种具有免疫缺陷的晚期视网膜变性的小鼠模型,NOG-rd1-2J 和 NOG-rd10,并对疾病进展和免疫缺陷状态进行了特征描述。我们还将人 ESC 衍生的视网膜片移植到 NOG-rd1-2J 中,并证实了它们的长期存活和结构化移植物感光细胞层的成熟,没有排斥或肿瘤形成。我们使用多电极阵列系统记录了来自宿主神经节细胞的光反应;这一结果与全组织免疫染色一致,表明在反应部位形成了宿主-移植物突触。这项研究展示了我们的小鼠模型的应用,并为临床使用人 ESC 衍生的视网膜片提供了概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bac/5918611/a169f5d11adf/gr1.jpg

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