Journal
CELL TRANSPLANTATION
Volume 19, Issue 4, Pages 487-503Publisher
COGNIZANT COMMUNICATION CORP
DOI: 10.3727/096368909X486057
Keywords
Stem cell; Migration; Transplantation; Degeneration; Muller glia
Funding
- Wellcome Trust [082217]
- Medical Research Council UK [G03000341]
- Department of Health's National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital
- Medical Research Council [G0700438, G0601588] Funding Source: researchfish
- National Institute for Health Research [NF-SI-0508-10130] Funding Source: researchfish
- Great Ormond Street Hospital Childrens Charity [V1221] Funding Source: researchfish
- MRC [G0601588, G0700438] Funding Source: UKRI
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Diseases culminating in photoreceptor loss are a major cause of untreatable blindness. Transplantation of rod photoreceptors is feasible, provided donor cells are at an appropriate stage of development when transplanted. Nevertheless, the proportion of cells that integrate into the recipient outer nuclear layer (ONL) is low. The outer limiting membrane (OLM), formed by adherens junctions between Muller glia and photoreceptors, may impede transplanted cells from migrating into the recipient ONL. Adaptor proteins such as Crumbs homologue 1 (Crb1) and zona occludins (ZO-1) are essential for localization of the OLM adherens junctions. We investigated whether targeted disruption of these proteins enhances donor cell integration. Transplantation of rod precursors in wild-type mice achieved 949 +/- 141 integrated cells. By contrast, integration is significantly higher when rod precursors are transplanted into Crb1(rd8/rd8) mice, a model of retinitis pigmentosa and Lebers congenital amaurosis that lacks functional CRB1 protein and displays disruption of the OLM (7,819 +/- 1,297; maximum 15,721 cells). We next used small interfering (si)RNA to transiently reduce the expression of ZO-1 and generate a reversible disruption of the OLM. ZO-1 knockdown resulted in similar, significantly improved, integration of transplanted cells in wild-type mice (7,037 +/- 1,293; maximum 11,965 cells). Finally, as the OLM remains largely intact in many retinal disorders, we tested whether transient ZO-1 knockdown increased integration in a model of retinitis pigmentosa, the rho(-/-) mouse; donor cell integration was significantly increased from 313 +/- 58 cells without treatment to 919 +/- 198 cells after ZO-1 knockdown. This study shows that targeted disruption of OLM junctional proteins enhances integration in the wild-type and degenerating retina and may be a useful approach for developing photoreceptor transplantation strategies.
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