Anti-Angiogenic and Anti-Inflammatory Effects of SERPINA3K on Corneal Injury
Author(s) -
Xiaochen Liu,
Zhirong Lin,
Tong Zhou,
Ronrong Zong,
Hui He,
Zhen Liu,
Jianxing Ma,
Zuguo Liu,
Yueping Zhou
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0016712
Subject(s) - cornea , corneal neovascularization , inflammation , corneal epithelium , neovascularization , corneal inflammation , vascular endothelial growth factor , pedf , angiogenesis , tumor necrosis factor alpha , epithelium , wound healing , vascular endothelial growth factor a , medicine , pathology , immunology , cancer research , ophthalmology , vegf receptors
SERPINA3K is a member of the serine proteinase inhibitor (SERPIN) family. Here we evaluated the therapeutic effects of SERPINA3K on neovascularization and inflammation in a rat cornea alkali burn model that is commonly employed to study corneal wounding. Topical treatment of the injured rat cornea with SERPINA3K (20 µg/eye/day) for 7 days significantly decreased the neovascular area, compared with the groups treated with BSA or PBS. The SERPINA3K treatment also ameliorated the corneal inflammation as evaluated by the inflammatory index. Furthermore, SERPINA3K enhanced the recovery of corneal epithelium after the alkali injury. Toward the mechanism of action, SERPINA3K down-regulated the expression of the pro-angiogenic and pro-inflammatory factors, vascular endothelial growth factor and tumor necrosis factor-α and up-regulated the expression of the anti-angiogenic factor, pigment epithelium-derived factor. SERPINA3K specifically inhibited growth of vascular endothelial cells. Meanwhile, SERPINA3K significantly up-regulated the expression of EGFR in the corneal epithelium. These findings suggest that SERPINA3K has therapeutic potential for corneal inflammation and NV.
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