IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


(Investigative Ophthalmology and Visual Science. 2004;45:3337-3348.)
© 2004 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.04-0193

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (14)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tezel, T. H.
Right arrow Articles by Kaplan, H. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tezel, T. H.
Right arrow Articles by Kaplan, H. J.

Reengineering of Aged Bruch’s Membrane to Enhance Retinal Pigment Epithelium Repopulation

Tongalp H. Tezel,1 Lucian V. Del Priore,2 and Henry J. Kaplan1

1From the Department of Ophthalmology and Visual Sciences, Kentucky Lions Eye Center, University of Louisville School of Medicine, Louisville, Kentucky; and 2The Edward S. Harkness Eye Institute, Department of Ophthalmology, Columbia University, New York, New York.

PURPOSE. An earlier study showed that age-related changes in the inner collagen layer (ICL) inhibit RPE cell repopulation of human Bruch’s membrane. The present study was undertaken to determine the effect of cleaning and/or an extracellular matrix (ECM) protein coating on the reattachment, apoptosis, proliferation, and final surface coverage of the transplanted RPE cells.

METHODS. Explants of aged Bruch’s membrane with ICL exposed were prepared from five human cadaveric eyes (donor ages, 69–84 years) and treated with Triton X-100 and/or coated with a mixture of laminin (330 µg/mL), fibronectin (250 µg/mL), and vitronectin (33 µg/mL). Viable human fetal and ARPE-19 cells (n = 15,000) were plated onto the surface and the RPE reattachment, apoptosis, and proliferation ratios were determined on the modified surfaces. Cells were cultured up to 17 days to determine the surface coverage. Ultrastructure of the modified Bruch’s membrane and RPE morphology were studied with transmission and scanning electron microscopy.

RESULTS. Reattachment ratios of fetal human RPE and ARPE-19 cells were similar on aged ICL (41.5% ± 1.7% and 42.9% ± 2.7%, P > 0.05). The reattachment ratio increased with ECM protein coating and decreased with detergent treatment. Combined cleaning and coating restored the reattachment ratio of the fetal RPE cells, but failed to increase the reattachment ratio of ARPE-19 cells. The highest apoptosis was observed on untreated ICL. Cleaning and the combined procedure of cleaning and ECM protein coating decreased fetal RPE cell apoptosis. Only RPE cells plated on cleaned or cleaned and ECM-coated ICL demonstrated proliferation that led to substantial surface coverage at day 17.

CONCLUSIONS. Age-related changes that impair RPE repopulation of Bruch’s membrane can be significantly reversed by combined cleaning and ECM protein coating of the ICL. Development of biologically tolerant techniques for modifying the ICL in vivo may enhance reattachment of the RPE and its repopulation of aged ICL.





This article has been cited by other articles:


Home page
Arch OphthalmolHome page
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]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the Association for Research in Vision and Ophthalmology