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通过细胞外基质蛋白Del-1的基因递送实现缺血组织的新生血管形成。

Neovascularization of ischemic tissues by gene delivery of the extracellular matrix protein Del-1.

作者信息

Zhong Jingping, Eliceiri Brian, Stupack Dwayne, Penta Kalyani, Sakamoto Gordon, Quertermous Thomas, Coleman Mike, Boudreau Nancy, Varner Judith A

机构信息

Comprehensive Cancer Center, University of California, San Diego, La Jolla, California 92093-0912, USA.

出版信息

J Clin Invest. 2003 Jul;112(1):30-41. doi: 10.1172/JCI17034.

Abstract

The ECM protein Del-1 is one of several novel ECM proteins that accumulate around angiogenic blood vessels in embryonic and tumor tissue and promote angiogenesis in the absence of exogenous growth factors. Del-1 expressed in mouse or rabbit ischemic hind-limb muscle by gene transfer rapidly promotes new blood vessel formation and restores muscle function. This angiogenic ECM protein initiates angiogenesis by binding to integrin alphavbeta5 on resting endothelium, thereby resulting in expression of the transcription factor Hox D3 and integrin alphavbeta3. Hox D3 converts resting endothelium to angiogenic endothelium by inducing expression of proangiogenic molecules such as integrin alphavbeta3. These findings provide evidence for an angiogenic switch that can be initiated in the absence of exogenous growth factors and indicate that the angiogenic matrix protein Del-1 may be a useful tool for the therapy of ischemic disease.

摘要

细胞外基质蛋白Del-1是几种新型细胞外基质蛋白之一,在胚胎组织和肿瘤组织中,它会在血管生成的血管周围聚集,并在没有外源性生长因子的情况下促进血管生成。通过基因转移在小鼠或兔缺血后肢肌肉中表达的Del-1能迅速促进新血管形成并恢复肌肉功能。这种血管生成的细胞外基质蛋白通过与静息内皮细胞上的整合素αvβ5结合来启动血管生成,从而导致转录因子Hox D3和整合素αvβ3的表达。Hox D3通过诱导促血管生成分子如整合素αvβ3的表达,将静息内皮细胞转化为血管生成内皮细胞。这些发现为在没有外源性生长因子的情况下启动血管生成开关提供了证据,并表明血管生成基质蛋白Del-1可能是治疗缺血性疾病的有用工具。

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