Evaluation of the Surgical Device and Procedure for Extracellular Matrix-Scaffold-Supported Human iPSC-Derived Retinal Pigment Epithelium Cell Sheet Transplantation

被引:34
作者
Kamao, Hiroyuki [1 ,2 ]
Mandai, Michiko [1 ]
Ohashi, Wataru [3 ]
Hirami, Yasuhiko [4 ]
Kurimoto, Yasuo [4 ]
Kiryu, Junichi [2 ]
Takahashi, Masayo [1 ]
机构
[1] RIKEN Ctr Dev Biol, Lab Retinal Regenerat, Chuo Ku, Kobe, Hyogo, Japan
[2] Kawasaki Med Sch, Dept Ophthalmol, Kurashiki, Okayama, Japan
[3] Japan Anim Care Corp, Meguro Ku, Tokyo, Japan
[4] Inst Biomed Res & Innovat Hosp, Chuo Ku, Kobe, Hyogo, Japan
关键词
induced pluripotent stem cell; retinal pigment epithelium; device; PLURIPOTENT STEM-CELLS; GENERATION; TISSUE; RABBIT; MOUSE;
D O I
10.1167/iovs.16-19778
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. To develop a clinically applicable transplantation device and surgical procedure for extracellular matrix-scaffold-supported human-induced pluripotent stem cell-derived retinal pigment epithelium (hiPSC-RPE) cell sheet transplantation for clinical use. METHODS. The developed surgical device consisted of a custom-designed hand piece and a cannula. The subretinal transplantation of hiPSC-RPE cell sheets was performed in 12 rabbits. The results evaluated were the graft condition (damage or fold), side (front or back), position (center, near, far), and direction (anterior, posterior, right, left) immediately after surgery and the graft condition (shrinking or fold) 2 weeks after surgery. These results were evaluated by fundus photography and optical coherence tomography, followed by immersion-fixed histology. RESULTS. All grafts could be transplanted without obvious damage. The transplanted grafts included 2 of 12 folded grafts, 12 of 12 front side, 12 of 12 center position, 10 of 12 anterior direction, and 2 of 12 right direction immediately after surgery, whereas transplantation with a distance between an inlet and an outlet greater than graft and the coaxial direction of the flow paths and the insertion device posed the correct condition and direction. Two weeks after the surgery, the transplanted grafts included two folded grafts and four shrunken grafts; however, complete drainage of subretinal fluid for adhesion between the graft and the host prevented shrunken grafts. CONCLUSIONS. A developed surgical device and procedure allow grafts to be transplanted into the targeted transplantation site safely and reproducibly. This surgical method will provide additional information on the advancement of future RPE transplantation therapies.
引用
收藏
页码:211 / 220
页数:10
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