Grafting of ARPE-19 and Schwann cells to the subretinal space in RCS rats

被引:57
作者
Wang, SM
Lu, B
Wood, P
Lund, RD [1 ]
机构
[1] Univ Utah, Hlth Sci Ctr, John A Moran Eye Ctr, Salt Lake City, UT 84132 USA
[2] Univ Miami, Sch Med, Miami Project Cure Paralysis, Miami, FL USA
关键词
D O I
10.1167/iovs.05-0279
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose. To study the distribution of the human retinal pigment epithelium (hRPE) cell line ARPE-19 and human Schwann (hSC) cells grafted to the subretinal space of the Royal College of Surgeon (RCS) rat and the relation of graft cell distribution to photoreceptor rescue. Methods. Cell suspensions of both donor types were injected into the subretinal space of 3-week-old dystrophic RCS rats through a transscleral approach, human fibroblast and medium were used as control grafts. All animals were maintained on oral cyclosporine. At 1, 2, 4, 6, 15, 28, and 36 weeks after grafting, animals were killed. Human cell-specific markers were used to localize donor cells. Results. Both donor cell types, as revealed by antibodies survived for a substantial time. Their distribution was very different: hRPE cells formed a large clump early on and, with time, spread along the host RPE in a layer one to two cells deep, whereas hSCs formed many smaller clumps, mainly in the subretinal space. Both cells rescued photoreceptors beyond the area of donor cell distribution. The number of surviving cells declined with time. Conclusions. Both hRPE and hSC grafts can survive and rescue photoreceptors for a substantial time after grafting. The number of both donor cell types declined with time, which could be an immune-related problem and/or due to other factors intrinsic to the host RCS retina. The fact that rescue occurred beyond the area of donor cell distribution suggests that diffusible factors are involved, raising the possibility that the two cell types function in a similar manner to rescue photoreceptors.
引用
收藏
页码:2552 / 2560
页数:9
相关论文
共 54 条
[1]   ESTIMATION OF NUCLEAR POPULATION FROM MICROTOME SECTIONS [J].
ABERCROMBIE, M .
ANATOMICAL RECORD, 1946, 94 (02) :239-247
[2]   TRANSPLANTATION OF FETAL RETINAL-PIGMENT EPITHELIUM IN AGE-RELATED MACULAR DEGENERATION WITH SUBFOVEAL NEOVASCULARIZATION [J].
ALGVERE, PV ;
BERGLIN, L ;
GOURAS, P ;
SHENG, YH .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1994, 232 (12) :707-716
[3]   Iris pigment epithelial cells: a possible cell source for the future treatment of neurodegenerative diseases [J].
Arnhold, S ;
Semkova, I ;
Andressen, C ;
Lenartz, D ;
Meissner, G ;
Sturm, V ;
Kochanek, S ;
Addicks, K ;
Schraermeyer, U .
EXPERIMENTAL NEUROLOGY, 2004, 187 (02) :410-417
[4]  
Casella CTB, 1996, GLIA, V17, P327, DOI 10.1002/(SICI)1098-1136(199608)17:4<327::AID-GLIA7>3.0.CO
[5]  
2-W
[6]   Adenovirus-mediated gene transfer of ciliary neurotrophic factor can prevent photoreceptor degeneration in the retinal degeneration (rd) mouse [J].
Cayouette, M ;
Gravel, C .
HUMAN GENE THERAPY, 1997, 8 (04) :423-430
[7]  
Cayouette M, 1998, J NEUROSCI, V18, P9282
[8]   Pigment epithelium-derived factor delays the death of photoreceptors in mouse models of inherited retinal degenerations [J].
Cayouette, M ;
Smith, SB ;
Becerra, SP ;
Gravel, C .
NEUROBIOLOGY OF DISEASE, 1999, 6 (06) :523-532
[9]  
CHAITIN MH, 1983, INVEST OPHTH VIS SCI, V24, P812
[10]  
Chong NHV, 1999, INVEST OPHTH VIS SCI, V40, P1298