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


     


(Investigative Ophthalmology and Visual Science. 2007;48:1245-1252.)
© 2007 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.06-0949

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 Google Scholar
Google Scholar
Right arrow Articles by O’Connor, M. D.
Right arrow Articles by McAvoy, J. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by O’Connor, M. D.
Right arrow Articles by McAvoy, J. W.

In Vitro Generation of Functional Lens-Like Structures with Relevance to Age-Related Nuclear Cataract

Michael D. O’Connor1,2,3 and John W. McAvoy1,2,4

1From the Save Sight Institute and the 2Department of Anatomy and Histology, University of Sydney, Sydney, New South Wales, Australia; and 4The Vision CRC, University of New South Wales, Sydney, New South Wales, Australia.

PURPOSE. To investigate the capacity of lens epithelial cells, maintained in a modified explant culture system, to mimic normal patterns of lens cell differentiation and to regenerate lens structure and function.

METHODS. Lens epithelial explants were set up in pairs with their apical surfaces facing each other. These explant pairs (EPs) were then cultured in vitreous for up to 43 days to promote their growth and differentiation. Immunohistochemistry and conventional light and electron microscopy were used to assess structural and functional properties of the lens-like structures that developed from EPs.

RESULTS. EPs that were asymmetrically exposed to vitreous routinely produced biconvex, lens-like structures composed of ordered epithelial and fiber cells that were transparent and had some focusing and magnifying ability. In addition, characteristic of the lens in vivo, fiberlike cells that were peripherally situated in EPs contained markers of the relatively early stages of fiber differentiation, whereas centrally situated cells contained markers of terminally differentiated fibers. During long-term culture of the EPs, a central opacity appeared that had structural features similar to those reported for the early stages of human, age-related nuclear cataract.

CONCLUSIONS. This study shows that, given appropriate culture conditions, lens epithelial cells can regenerate ordered lens-like structures with functional properties. This system represents a valuable new tool for the investigation of factors involved in the generation of normal lens structure and function and lens opacification.








HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Association for Research in Vision and Ophthalmology