Role of Lumican in the Corneal Epithelium during Wound Healing

Shizuya Saika(University of Cincinnati), Atsushi Shiraishi(University of Cincinnati), Satoko Saika(University of Cincinnati), Chia‐Yang Liu(University of Cincinnati), James L. Funderburgh(University of Pittsburgh), Candace W.-C. Kao(University of Cincinnati), Richard Converse(University of Cincinnati), Winston W.‐Y. Kao(University of Cincinnati)
Journal of Biological Chemistry
January 1, 2000
Cited by 234Open Access
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Abstract

Lumican regulates collagenous matrix assembly as a keratan sulfate proteoglycan in the cornea and is also present in the connective tissues of other organs and embryonic corneal stroma as a glycoprotein. In normal unwounded cornea, lumican is expressed by stromal keratocytes. Our data show that injured mouse corneal epithelium ectopically and transiently expresses lumican during the early phase of wound healing, suggesting a potential lumican functionality unrelated to regulation of collagen fibrillogenesis, e. g. modulation of epithelial cell adhesion or migration. An anti-lumican antibody was found to retard corneal epithelial wound healing in cultured mouse eyes. Healing of a corneal epithelial injury in Lum(-/-) mice was significantly delayed compared with Lum(+/-) mice. These observations indicate that lumican expressed in injured epithelium may modulate cell behavior such as adhesion or migration, thus contributing to corneal epithelial wound healing.


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