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(Investigative Ophthalmology and Visual Science. 1999;40:1822-1828.)
© 1999 by The Association for Research in Vision and Ophthalmology, Inc.

Inhibition of Vascular Endothelial Cell Morphogenesis in Cultures by Limbal Epithelial Cells

David Hui-Kang Ma1, Ray Jui-Fang Tsai1, Wing-Keung Chu2, Cheng-Heng Kao3 and Jan-Kan Chen2

1 From the Department of Ophthalmology, Chang Gung Memorial Hospital, Tao-Yuan, Taiwan; and the 2 Department of Physiology and 3 Center of General Education, College of Medicine, Chang Gung University, Tao-Yuan, Taiwan, Republic of China.

PURPOSE. To study the in vitro angiogenic activity of human conjunctival and limbal epithelial cells and conjunctival, limbal, and corneal fibroblasts in a three-cell-type coculture model.

METHODS. Human umbilical vein endothelial cells (EC) were cocultured with epithelial cells, fibroblasts, or epithelial cells and fibroblasts to test their effect on EC morphogenesis. Neutralizing antibodies to some known angiogenic factors were added to the culture to see whether the EC morphogenesis may be blocked by a particular antibody.

RESULTS. Conjunctival and limbal epithelial cells exhibited very little or no stimulatory effect on EC tube formation when examined in an EC–epithelial cell coculture system. In contrast, conjunctival, limbal, and corneal fibroblasts all promoted EC morphogenesis when examined under the same culture conditions. Fibroblast-induced EC morphogenesis was inhibited by addition of anti-vascular endothelial growth factor (VEGF) and/or anti-basic fibroblast growth factor (bFGF) antibodies to the culture medium. In the three-cell-type coculture system consisting of ECs, fibroblasts, and epithelial cells, limbal epithelial cells (but not conjunctival epithelial cells) exhibited a strong inhibitory effect on fibroblast-induced EC tube formation.

CONCLUSIONS. The proangiogenic activity of ocular surface fibroblasts is probably mediated through a paracrine mechanism by VEGF and bFGF. Limbal epithelial cells, but not conjunctival epithelial cells, inhibit fibroblast-stimulated angiogenesis.




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