Peng Qing, Thomas Biju B, Aramant Robert B, Chen Zhenhai, Sadda Srinivas R, Seiler Magdalene J
Department of Ophthalmology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Curr Eye Res. 2007 Sep;32(9):781-9. doi: 10.1080/02713680701530597.
To evaluate retinal sheet transplants in S334ter-line-3 retinal degenerate rats by comparing visual responses recorded electrophysiologically with morphology based on light and electron microscopy.
S334ter-line-3 retinal degenerate rats (n = 7) received retinal sheet transplants between postnatal days 28 and 31. The donor tissue was derived from transgenic embryonic day 19 (E19) rat retinae expressing human placental alkaline phosphatase (hPAP). Fresh retinal sheets were gently transplanted into the subretinal space of the left eye with the help of a custom-made implantation tool. Selected rats (n = 5) were subjected to electrophysiologic evaluation of visual responses from the superior colliculus about 84-121 days after surgery. Transplanted eyes were processed for light microscopy (LM) and electron microscopy (EM) evaluations.
All the transplanted rats that were evaluated for visual responses in the brain showed responses to very low light stimulation (-3.42 to -2.8 log cd/m(2)) of the eye in a small area of the superior colliculus corresponding with the placement of the transplant in the host retina. Histologic evaluation showed that most of the transplants contained well-laminated areas with correct polarity in the subretinal space. Inside the transplant areas, rosettes of photoreceptors with inner and outer segments were found. In the laminated areas, the outer segments of photoreceptors were facing the host retinal pigment epithelium (RPE). Immunohistochemical evaluation of hPAP donor cells revealed areas with specific staining of the transplants in the subretinal space. Electron microscopic evaluation showed a glial demarcation membrane between the host and the transplant, however, processes originating from the transplant were observed inside the host retina.
Sheets of E19 rat retina transplanted into the subretinal space of S334ter-line-3 rats survived without immune rejection and continued to show visual function when tested after 3 months. Well-developed photoreceptors and many synapse types were seen within the transplants. hPAP staining showed a certain degree of integration between the host retina and the transplant suggesting that transplanted photoreceptors contributed to the restored light sensitivity.
通过比较电生理记录的视觉反应与基于光镜和电镜的形态学,评估S334ter-3系视网膜变性大鼠的视网膜片移植情况。
7只S334ter-3系视网膜变性大鼠在出生后第28至31天接受视网膜片移植。供体组织来源于表达人胎盘碱性磷酸酶(hPAP)的转基因胚胎第19天(E19)大鼠视网膜。借助定制的植入工具,将新鲜的视网膜片轻轻移植到左眼的视网膜下间隙。在术后约84 - 121天,对选定的5只大鼠进行上丘视觉反应的电生理评估。对移植眼进行光镜(LM)和电镜(EM)评估。
所有接受脑部视觉反应评估的移植大鼠,在上丘与移植片在宿主视网膜中的位置相对应的小区域内,对眼睛的极低光刺激(-3.42至-2.8 log cd/m²)均有反应。组织学评估显示,大多数移植片在视网膜下间隙包含排列良好且极性正确的区域。在移植区域内,发现了具有内段和外段的光感受器玫瑰花结。在排列区域中,光感受器的外段朝向宿主视网膜色素上皮(RPE)。对hPAP供体细胞的免疫组织化学评估显示,视网膜下间隙的移植片有特异性染色区域。电镜评估显示宿主与移植片之间有神经胶质分界膜,然而,在宿主视网膜内部观察到源自移植片的突起。
移植到S334ter-3系大鼠视网膜下间隙的E19大鼠视网膜片存活且未发生免疫排斥,3个月后测试时仍显示视觉功能。移植片内可见发育良好的光感受器和多种突触类型。hPAP染色显示宿主视网膜与移植片之间有一定程度的整合,表明移植的光感受器有助于恢复光敏感性。