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Invest Ophthalmol Vis Sci ; 47(4): 1352-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16565368

ABSTRACT

PURPOSE: The study was conducted to elucidate the detailed expression pattern of angiogenesis-related factors in human ocular surface epithelium. The focus was factors with significantly higher gene expression in corneal epithelium (CE) than in conjunctival epithelium (CJE). METHODS: The relative gene expression of 36 angiogenesis-related factors was compared in human CE and CJE, by using the introduced amplified fragment-length polymorphism (iAFLP) METHOD: Also examined were the expression patterns in the CE, limbal epithelium (LE), and CJE of factors with significantly higher expression in the CE, by using real-time PCR, in situ hybridization, immunohistochemistry, and immunoelectron microscopy. RESULTS: Only thrombospondin (TSP)-1 exhibited significantly higher expression in the CE. In situ hybridization and real-time PCR showed TSP-1 transcripts in the basal cells of the CE and LE. Compared with the CJE, they were significantly upregulated at those sites. Immunohistochemistry revealed that TSP-1 was strongly expressed in the basal region of the CE. Its expression was faint in LE and absent in CJE. Immunoelectron microscopy revealed that the CE and LE demonstrated TSP-1 labeling just below the epithelium, in the basal region of basal cells, and occasionally in the basal cell membrane. There was little or no labeling in the CJE. CONCLUSIONS: In the human ocular surface epithelium, basal cells of the CE and LE, but not of the CJE, synthesize TSP-1. High levels of TSP-1 are present only just below the CE. Its unique distribution may be related to corneal avascularity and integrity.


Subject(s)
Conjunctiva/metabolism , Epithelium, Corneal/metabolism , Thrombospondin 1/genetics , Thrombospondin 1/metabolism , Angiogenic Proteins/genetics , Angiogenic Proteins/metabolism , Conjunctiva/ultrastructure , DNA Primers/chemistry , Epithelium/metabolism , Epithelium/ultrastructure , Epithelium, Corneal/ultrastructure , Gene Amplification , Gene Expression Regulation , Humans , Immunohistochemistry , In Situ Hybridization , Microscopy, Immunoelectron , Middle Aged , Polymorphism, Restriction Fragment Length , Reverse Transcriptase Polymerase Chain Reaction , Thrombospondin 1/ultrastructure , Up-Regulation
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