Reiss Yvonne
Institute of Neurology/Edinger Institute, Frankfurt University Medical School, Heinrich-Hoffmann-Strasse, 760528, Frankfurt, Germany.
Recent Results Cancer Res. 2010;180:3-13. doi: 10.1007/978-3-540-78281-0_2.
The formation of new blood vessels plays an important role during the development and progression of a disease. In recent years, there has been a tremendous effort to uncover the molecular mechanisms that drive blood vessel growth in adult tissues. Angiopoietins belong to a family of growth factors that are critically involved in blood vessel formation during developmental and pathological angiogenesis. The importance of Angiopoietin signaling has been recognized in transgenic mouse models as the genetic ablation of Ang-1, and its primary receptor Tie2 has led to early embryonic lethality. Interesting and unusual for a family of ligands, Ang-2 has been identified as an antagonist of Ang-1 in endothelial cells as evidenced by a similar embryonic phenotype when Ang-2 was overexpressed in transgenic mice. In this review, we focus on the functional consequences of autocrine Angiopoietin signaling in endothelial cells.
新血管的形成在疾病的发展和进程中起着重要作用。近年来,人们付出了巨大努力来揭示驱动成体组织中血管生长的分子机制。血管生成素属于一类生长因子家族,在发育性和病理性血管生成过程中,它们对血管形成至关重要。血管生成素信号传导的重要性在转基因小鼠模型中已得到认可,因为血管生成素-1(Ang-1)及其主要受体Tie2的基因敲除会导致早期胚胎致死。作为一类配体,有趣且不同寻常的是,血管生成素-2(Ang-2)已被确定为内皮细胞中Ang-1的拮抗剂,转基因小鼠中过表达Ang-2时出现的类似胚胎表型证明了这一点。在本综述中,我们重点关注内皮细胞中自分泌血管生成素信号传导的功能后果。