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血管生成对血管整合素αvβ3的需求。

Requirement of vascular integrin alpha v beta 3 for angiogenesis.

作者信息

Brooks P C, Clark R A, Cheresh D A

机构信息

Department of Immunology, Scripps Research Institute, La Jolla, CA 92037.

出版信息

Science. 1994 Apr 22;264(5158):569-71. doi: 10.1126/science.7512751.

Abstract

Angiogenesis depends on the adhesive interactions of vascular cells. The adhesion receptor integrin alpha v beta 3 was identified as a marker of angiogenic vascular tissue. Integrin alpha v beta 3 was expressed on blood vessels in human wound granulation tissue but not in normal skin, and it showed a fourfold increase in expression during angiogenesis on the chick chorioallantoic membrane. In the latter assay, a monoclonal antibody to alpha v beta 3 blocked angiogenesis induced by basic fibroblast growth factor, tumor necrosis factor-alpha, and human melanoma fragments but had no effect on preexisting vessels. These findings suggest that alpha v beta 3 may be a useful therapeutic target for diseases characterized by neovascularization.

摘要

血管生成依赖于血管细胞的黏附相互作用。黏附受体整合素αvβ3被鉴定为血管生成性血管组织的标志物。整合素αvβ3在人类伤口肉芽组织的血管上表达,但在正常皮肤中不表达,并且在鸡胚绒毛尿囊膜血管生成过程中其表达增加了四倍。在后一种实验中,一种针对αvβ3的单克隆抗体可阻断碱性成纤维细胞生长因子、肿瘤坏死因子-α和人类黑色素瘤片段诱导的血管生成,但对已有的血管没有影响。这些发现表明,αvβ3可能是针对以新血管形成为特征的疾病的有用治疗靶点。

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