Rescue effects of IPE transplants in RCS rats: short-term results.

PURPOSE The aim of this study was to investigate the possible rescue effect of subretinal iris pigment epithelial (IPE) cell transplantation in Royal College of Surgeons (RCS) rats by light and electron microscopic histology. METHODS IPE cells were harvested from 20- to 26-day-old Long-Evans rats and were directly trans planted transsclerally into the subretinal space of 32 16- to 20-day-old RCS rats using a 32-gauge Hamilton syringe. Specimens of transplanted eyes were embedded for electron microscopy after 8 weeks. Specimens from the iris and retinal pigment epithelium (RPE) of Long-Evans rats and RPE from RCS rats without surgical treatment were also embedded. Sham surgery was also performed in 8 eyes. RESULTS The IPE cells transplanted into the subretinal space were localized between host RPE and retina, had round cell shapes without polar organization, and contained phagosomes resulting from rod outer segment (ROS) uptake. The underlying host RPE cells were heavily pigmented. RPE cells from RCS rats revealed fragmentation of endoplasmic reticulum, which distinguishes them ultrastructurally from pigment epithelial cells of Long-Evans rats. Ultrastructural alterations were observed in the cytoplasm of transplanted cells. Melanin granules in the IPE cells were found in large vacuoles, which also contained phagosomes originating from ROS uptake. In 13 eyes, 1 to 4 rows and 5 to 8 rows of saved photoreceptors were detected facing transplanted IPE cells in 6 (46%) and 4 (31%) eyes, respectively, 2 months after surgery. However, in 10 (53%) and 7 (37%) of 19 eyes, 1 to 4 rows and 5 to 8 rows, respectively, were also found at sites without IPE cells in the plane of section. ROS directed toward transplanted IPE cells were seen in one case, but these rods were shortened and disorganized. At most sites between transplanted cells and inner segments of photoreceptors, outer segments and cellular debris were absent. In eyes without transplanted cells no photoreceptor cells were alive at the age of 2 months. After sham surgery 6 (75%) eyes had 1 to 4 rows and 2 (25%) 5 to 8 rows of photoreceptors. CONCLUSIONS Transplanted IPE cells can take up and degrade ROS in vivo in RCS rats. Uptake of ROS alters the morphology of pigment granules in transplanted IPE cells. Pigmentation is an uncertain marker for identifying transplanted pigment cells. IPE transplants are not as good as RPE transplants in rescuing photoreceptors. However, there is a significant difference between transplanted eyes and nontreated eyes. The rescue effect of IPE cells was not significantly different from that of sham surgery.

[1]  P. Gouras,et al.  Retinal pigment epithelial transplants and retinal function in RCS rats. , 1993, Investigative ophthalmology & visual science.

[2]  Nitin R. Patel,et al.  A Network Algorithm for Performing Fisher's Exact Test in r × c Contingency Tables , 1983 .

[3]  H. Sheedlo,et al.  Long-term rescue of photoreceptor cells in the retinas of RCS dystrophic rats by RPE transplants. , 1990, Progress in brain research.

[4]  S. Orlow Melanosomes are specialized members of the lysosomal lineage of organelles. , 1995, The Journal of investigative dermatology.

[5]  Klaus Heimann,et al.  Retinal pigment epithelial cells from Royal College of Surgeons dystrophic rats can take up melanin granules , 1999, Graefe's Archive for Clinical and Experimental Ophthalmology.

[6]  J. T. Ernest,et al.  A new method of culturing and transferring iris pigment epithelium. , 1997, Investigative ophthalmology & visual science.

[7]  K Heimann,et al.  Iris pigment epithelial cells of long evans rats demonstrate phagocytic activity. , 1997, Experimental eye research.

[8]  K. Heimann,et al.  Melanin granules of retinal pigment epithelium are connected with the lysosomal degradation pathway. , 1999, Experimental eye research.

[9]  P. Wiedemann,et al.  Porcine iris pigment epithelial cells can take up retinal outer segments. , 1997, Experimental eye research.

[10]  R. Sidman,et al.  Congenic strains of RCS rats with inherited retinal dystrophy. , 1975, The Journal of heredity.

[11]  U. Schraermeyer The intracellular origin of the melanosome in pigment cells: a review of ultrastructural data. , 1996, Histology and histopathology.

[12]  M. Lavail,et al.  Photoreceptor degeneration in inherited retinal dystrophy delayed by basic fibroblast growth factor , 1990, Nature.

[13]  T. Fitzpatrick,et al.  SUBCELLULAR LOCALIZATION OF MELANIN BIOSYNTHESIS , 1963, Annals of the New York Academy of Sciences.

[14]  S. Orlow,et al.  Lysosome-associated membrane protein-1 (LAMP-1) is the melanocyte vesicular membrane glycoprotein band II. , 1993, The Journal of investigative dermatology.

[15]  R. W. Young,et al.  Photoreceptor rescue in the dystrophic retina by transplantation of retinal pigment epithelium. , 1992, International review of cytology.

[16]  P. Gouras,et al.  Transplanted retinal pigment epithelium modifies the retinal degeneration in the RCS rat. , 1989, Investigative ophthalmology & visual science.

[17]  R. Caldwell,et al.  Increased vascular density and vitreo-retinal membranes accompany vascularization of the pigment epithelium in the dystrophic rat retina. , 1989, Current eye research.

[18]  S. E. Hughes,et al.  Photoreceptor rescue in the RCS rat without pigment epithelium transplantation. , 1990, Current eye research.

[19]  M. Horneber,et al.  Quantitative and morphological changes of the choroid vasculature in RCS rats and their congenic controls. , 1996, Experimental eye research.

[20]  K. Bartz-Schmidt,et al.  Descemet's membrane as membranous support in RPE/IPE transplantation. , 1997, Current eye research.

[21]  U. Schraermeyer Transport of endocytosed material into melanin granules in cultured choroidal melanocytes of cattle--new insights into the relationship of melanosomes with lysosomes. , 1995, Pigment cell research.

[22]  P. Gouras,et al.  Transplantation of retinal epithelium prevents photoreceptor degeneration in the RCS rat. , 1989, Progress in clinical and biological research.

[23]  Richard L. Sidman,et al.  INHERITED RETINAL DYSTROPHY IN THE RAT , 1962, The Journal of cell biology.

[24]  P. Gouras,et al.  Tolerance of Human Fetal Retinal Pigment Epithelium Xenografts in Monkey Retina. , 1997 .

[25]  J. Stone,et al.  Tissue oxygen during a critical developmental period controls the death and survival of photoreceptors. , 1997, Investigative ophthalmology & visual science.

[26]  V. Gaur,et al.  Transplantation to the diseased and damaged retina , 1991, Trends in Neurosciences.

[27]  R. J. Mullen,et al.  Inherited retinal dystrophy: primary defect in pigment epithelium determined with experimental rat chimeras. , 1976, Science.