血管生成素-1将Tie2固定在细胞间接触部位以及细胞外基质上。

Tie2 is tied at the cell-cell contacts and to extracellular matrix by angiopoietin-1.

作者信息

Fukuhara Shigetomo, Sako Keisuke, Noda Kazuomi, Nagao Kaori, Miura Koichi, Mochizuki Naoki

出版信息

Exp Mol Med. 2009 Mar 31;41(3):133-9. doi: 10.3858/emm.2009.41.3.016.

Abstract

Angiopoietin-1 (Ang1) binds to and activates Tie2 receptor tyrosine kinase. Ang1-Tie2 signal has been proposed to exhibit two opposite roles in the controlling blood vessels. One is vascular stabilization and the other is vascular angiogenesis. There has been no answer to the question as to how Tie2 induces two opposite responses to the same ligand. Our group and Dr. Alitalos group have demonstrated that trans-associated Tie2 at cell-cell contacts and extracellular matrix (ECM)-anchored Tie2 play distinct roles in the endothelial cells. The complex formation depends on the presence or absence of cell-cell adhesion. Here, we review how Ang1-Tie2 signal regulates vascular maintenance and angiogenesis. We further point to the unanswered questions that must be clarified to extend our knowledge of vascular biology and to progress basic knowledge to the treatment of the diseases in which Ang1-Tie2-mediated signal is central.

摘要

血管生成素-1(Ang1)与Tie2受体酪氨酸激酶结合并激活它。有人提出,Ang1-Tie2信号在控制血管方面具有两种相反的作用。一种是血管稳定,另一种是血管生成。关于Tie2如何对同一配体产生两种相反的反应,这个问题一直没有答案。我们团队和阿利塔洛斯博士的团队已经证明,细胞间接触时反式结合的Tie2以及细胞外基质(ECM)锚定的Tie2在内皮细胞中发挥着不同的作用。复合物的形成取决于细胞间粘附的存在与否。在这里,我们综述了Ang1-Tie2信号如何调节血管维持和血管生成。我们还指出了一些尚未解决的问题,这些问题必须得到澄清,以扩展我们对血管生物学的认识,并将基础知识应用于以Ang1-Tie2介导的信号为核心的疾病治疗中。

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