Aramant R B, Seiler M J, Ball S L
Department of Ophthalmology and Visual Sciences, University of Louisville, School of Medicine, Kentucky 40202, USA.
Invest Ophthalmol Vis Sci. 1999 Jun;40(7):1557-64.
Many retinal diseases, such as macular degeneration, affect both retinal pigment epithelium (RPE) and photoreceptors. Therefore, retinal repair may require transplantation of both tissues together as a cograft.
As recipients of retina-RPE cografts, 7- to 10-week-old albino Royal College of Surgeons rats that lose their photoreceptors because of a pigment epithelium defect were used. Freshly harvested intact sheets of RPE with neural retina from pigmented normal rat fetuses were gel embedded for protection and transplanted into the subretinal space.
After 6 to 7 weeks, with the support of the cografted RPE sheet, transplanted photoreceptors developed fully in organized parallel layers in the subretinal space. Immunohistochemistry for rhodopsin, rod alpha-transducin, and S-antigen and peanut agglutinin labeling for cone interphotoreceptor matrix domains suggested that the photoreceptors in the graft were capable of normal function.
Freshly harvested intact sheets of fetal RPE and retina, transplanted together into the subretinal space, can develop a normal morphology. Such transplants have the potential to benefit retinal diseases with dysfunctional RPE and photoreceptors.
许多视网膜疾病,如黄斑变性,会影响视网膜色素上皮(RPE)和光感受器。因此,视网膜修复可能需要将这两种组织作为联合移植体一起移植。
以7至10周龄因色素上皮缺陷而失去光感受器的白化皇家外科学院大鼠作为视网膜-RPE联合移植体的受体。从有色正常大鼠胎儿中新鲜获取的带有神经视网膜的完整RPE片层经凝胶包埋以进行保护,然后移植到视网膜下间隙。
6至7周后,在联合移植的RPE片层的支持下,移植的光感受器在视网膜下间隙中以有组织的平行层充分发育。视紫红质、视杆α-转导蛋白和S抗原的免疫组织化学以及视锥细胞间光感受器基质域的花生凝集素标记表明,移植体中的光感受器能够正常发挥功能。
新鲜获取的完整胎儿RPE和视网膜片层一起移植到视网膜下间隙中,可以形成正常的形态。这种移植有可能使患有RPE和光感受器功能障碍的视网膜疾病受益。