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(Investigative Ophthalmology and Visual Science. 2005;46:479-486.)
© 2005 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.04-1014

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Soluble Lumican Glycoprotein Purified from Human Amniotic Membrane Promotes Corneal Epithelial Wound Healing

Lung-Kun Yeh,1,2 Wei-Li Chen,3,4 Wei Li,5 Edgar M. Espana,5 Jie Ouyang,1 Tetsuya Kawakita,5 Winston W.-Y. Kao,3 Scheffer C. G. Tseng,5 and Chia-Yang Liu1

1From the Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida; the 2Department of Ophthalmology, Chang-Gung Memorial Hospital, Linko, Taiwan, Republic of China; the 3Department of Ophthalmology, University of Cincinnati College of Medicine, Cincinnati, Ohio; the 4Department of Ophthalmology, National Taiwan University Hospital, Taipei, Taiwan, Republic of China; and 5TissueTech, Inc. and Ocular Surface Center, Miami, Florida.

PURPOSE. To purify and characterize the glycoprotein lumican, isolated from human amniotic membrane (AM), and to examine its efficacy in treating corneal epithelium debridement.

METHODS. An affinity-purified, anti-human lumican antibody–conjugated protein A Sepharose column was used to purify soluble lumican protein from human AM. The purified AM lumican was characterized by two-dimensional and SDS gel electrophoresis, plus Western blot analysis with anti-lumican antibody. The effects of lumican on corneal epithelial wound healing were examined in an organ culture mouse eye model.

RESULTS. Lumican was found to be abundantly present in the stroma of human AM. It was extracted from the AM by isotonic, 1 M NaCl, and 4 M guanidine HCl solutions, suggesting that it is present in both the soluble and matrix-bound states. In two-dimensional gel electrophoresis, the 50-kDa human amniotic lumican purified by antibody-conjugated affinity chromatography migrated in a smear between pH 3.0 and 6.0. After endo-ß-galactosidase digestion, it existed as a single core protein at pH 6.0, suggesting that native human amniotic lumican is a glycoprotein with short sugar moiety. Addition of purified human AM lumican to cultured medium promoted re-epithelialization and enhanced cell proliferation of wild-type mouse corneal epithelial cells in an organ culture. In lumican-knockout (lum/) mice, the effect of human lumican on promoting corneal epithelial wound healing was even more dramatic than in wild-type mice.

CONCLUSIONS. The diversified functions of lumican include modulation of epithelial cells in wound healing and serving as an extracellular matrix component. Administration of lumican may be beneficial for treating epithelial defects in the cornea and other tissues.





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