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

被引:63
作者
Fukuhara, Shigetomo [1 ]
Sako, Keisuke [1 ]
Noda, Kazuomi [1 ]
Nagao, Kaori [1 ]
Miura, Koichi [1 ]
Mochizuki, Naoki [1 ]
机构
[1] Natl Cardiovasc Ctr, Res Inst, Dept Struct Anal, Osaka 5658565, Japan
关键词
angiopoietin-1; angiostatic proteins; cell movement; cell proliferation; extracellular signal-regulated MAP kinases; neovacularizaton; pathologic; neovascularization; physiologic; proto-oncogene proteins; c-akt; receptor; TIE-2; RECEPTOR TYROSINE KINASE; ENDOTHELIAL-CELLS; LIGAND ANGIOPOIETIN-2; E-SELECTIN; VE-PTP; ANGIOGENESIS; EXPRESSION; ACTIVATION; PHOSPHORYLATION; VASCULATURE;
D O I
10.3858/emm.2009.41.3.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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. Alitalo's 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.
引用
收藏
页码:133 / 139
页数:7
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