Expression of antisense to integrin subunit β3 inhibits microvascular endothelial cell capillary tube formation in fibrin

被引:33
作者
Dallabrida, SM
De Sousa, MA
Farrell, DH [1 ]
机构
[1] Oregon Hlth & Sci Univ, Sch Dent, Dept Oral Mol Biol, Portland, OR 97201 USA
[2] Penn State Univ, Coll Med, Dept Biochem & Mol Biol, Hershey, PA 17033 USA
关键词
D O I
10.1074/jbc.M001446200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
alpha(v)beta(3) antagonists are potent angiogenesis inhibitors, and several different classes of inhibitors have been developed, including monoclonal antibodies, synthetic peptides, and small organic molecules. However, each class of inhibitor works by the same principal, by blocking the binding of ligands to alpha(v)beta(3). In an effort to develop an alpha(v)beta(3) inhibitor that down-regulates the actual level of alpha(v)beta(3), we developed an antisense strategy to inhibit alpha(v)beta(3) expression in vitro. beta(3) antisense expressed in endothelial cells specifically down-regulated alpha(v)beta(3) and inhibited capillary tube formation, with the extent of down-regulation correlating with the extent of tube formation inhibition. This inhibition was matrix-specific, since tube formation was not inhibited in Matrigel. These findings support the notion that alpha(v)beta(3) is required for an essential step of angiogenesis in fibrin, namely capillary tube formation. These results suggest that pseudogenetic inhibition of beta(3) integrins using antisense techniques may ultimately provide a therapeutic means to inhibit angiogenesis in vivo.
引用
收藏
页码:32281 / 32288
页数:8
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