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1From the Institute of Ophthalmology and Visual Science, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, New Jersey; and the 2Department of Ophthalmology, Tohoku University, School of Medicine, Miyagi, Japan.
PURPOSE. To determine whether iris pigment epithelium (IPE) cells can attach to aged submacular human Bruchs membrane and to assess whether IPE cells express the integrin subunits that may be necessary to bind to the known extracellular matrix ligands present in Bruchs membrane.
METHODS. IPE cells were seeded onto the RPE basement membrane (RPEbm) or inner collagenous layer (ICL) of aged submacular Bruchs membrane as microaggregates or were expanded in culture until enough cells could be obtained for seeding. Cell morphology and the percentage of cell coverage were determined 1 or 7 days after seeding. Messenger RNA was extracted from cultured and uncultured IPE cells and analyzed by RT-PCR. The expression of integrin subunits
1 to
6 and ß1 mRNA was examined.
RESULTS. Coverage by uncultured IPE was low on both surfaces at day-1 (RPEbm, 7.9% ± 4.8%; ICL, 5.0% ± 2.5%) with few intact cells present. Culturing IPE improved attachment with similar coverage on both surfaces and no significant difference between day-1 (RPEbm, 89.9% ± 9.1%; ICL, 63.4% ± 26.5%) and day-7 (RPEbm, 97.8% ± 2.3%; ICL, 94.7% ± 6.6%). By day-7, cell morphology and coverage on both surfaces was variable, ranging from few intact cells to a high degree of coverage by flattened cells. All integrin subunits studied were expressed in cultured cells, whereas
2,
3, and
4 showed less or no expression in uncultured cells.
CONCLUSIONS. Upregulation of integrin mRNA expression may be one explanation for the difference in coverage by cultured versus uncultured IPE cells. The presence of dead, dying, or flattened cells at day 7 indicates that IPE may not survive or differentiate on aged submacular Bruchs membrane.
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H. Cai, M. C. Shin, T. H. Tezel, H. J. Kaplan, and L. V. Del Priore Use of iris pigment epithelium to replace retinal pigment epithelium in age-related macular degeneration: a gene expression analysis. Arch Ophthalmol, September 1, 2006; 124(9): 1276 - 1285. [Abstract] [Full Text] [PDF] |
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