Developing Rods Transplanted into the Degenerating Retina of Crx‐Knockout Mice Exhibit Neural Activity Similar to Native Photoreceptors123. (22nd May 2013)

• Record Type: Journal Article
• Authors: Homma, Kohei; Okamoto, Satoshi; Mandai, Michiko; Gotoh, Norimoto; Rajasimha, Harsha K.; Chang, Yi‐Sheng; Chen, Shan; Li, Wei; Cogliati, Tiziana; Swaroop, Anand; Takahashi, Masayo
• Is Part Of: Stem cells. Volume 31:Number 6(2013:Jun.)
• Page Start: 1149
• Page End: 1159
• Publication Date: 2013-05-22
• Subjects: Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.1372
• Languages: English
• ISSNs: 1066-5099

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Replacement of dysfunctional or dying photoreceptors offers a promising approach for retinal neurodegenerative diseases, including age‐related macular degeneration and retinitis pigmentosa. Several studies have demonstrated the integration and differentiation of developing rod photoreceptors when transplanted in wild‐type or degenerating retina; however, the physiology and function of the donor cells are not adequately defined. Here, we describe the physiological properties of developing rod photoreceptors that are tagged with green fluorescent protein (GFP) driven by the promoter of rod differentiation factor, <italic>Nrl</italic>. GFP‐tagged developing rods show Ca<sup>2 +</sup> responses and rectifier outward currents that are smaller than those observed in fully developed photoreceptors, suggesting their immature developmental state. These immature rods also exhibit hyperpolarization‐activated current (<italic>I</italic><sub>h</sub>) induced by the activation of hyperpolarization‐activated cyclic nucleotide‐gated (HCN) channels. When transplanted into the subretinal space of wild‐type or retinal degeneration mice, GFP‐tagged developing rods can integrate into the photoreceptor outer nuclear layer in wild‐type mouse retina and exhibit Ca<sup>2 +</sup> responses and membrane current comparable to native rod photoreceptors. A proportion of grafted rods develop rhodopsin‐positive outer segment‐like structures within 2 weeks after transplantation into the retina of Crx‐knockout mice and produce rectifier outward current and <italic>I</italic><sub>h</sub> upon membrane depolarization and hyperpolarization. GFP‐positive rods derived from induced pluripotent stem (iPS) cells also display similar membrane current <italic>I</italic><sub>h</sub> as native developing rod photoreceptors, express rod‐specific phototransduction genes, and HCN‐1 channels. We conclude that <italic>Nrl</italic>‐promoter‐driven GFP‐tagged donor photoreceptors exhibit physiological characteristics of rods and that iPS cell‐derived rods in vitro may provide a renewable source for cell‐replacement therapy. S<sc>TEM</sc> C<sc>ells</sc><italic>2013;31:1149–1159</italic></p> </abstract>