William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
PLoS One. 2010 Aug 23;5(8):e12323. doi: 10.1371/journal.pone.0012323.
Angiotensin (Ang) II and Ang-(1-7) are two of the bioactive peptides of the rennin-angiotensin system. Ang II is involved in the development of cardiovascular disease, such as hypertension and atherosclerosis, while Ang-(1-7) shows cardiovascular protection in contrast to Ang II.
METHODOLOGY/PRINCIPAL FINDINGS: In this study, we investigated effects of Ang II and Ang-(1-7) on vascular smooth muscle cell (SMC) proliferation and migration, which are critical in the formation of atherosclerotic lesions. Treatment with Ang II resulted in an increase of SMC proliferation, whereas Ang-(1-7) alone had no effects. However, preincubation with Ang-(1-7) inhibited Ang II-induced SMC proliferation. Ang II promoted SMC migration, and this effect was abolished by pretreatment with Ang-(1-7). The stimulatory effects of Ang II on SMC proliferation and migration were blocked by the Ang II receptor antagonist lorsartan, while the inhibitory effects of Ang-(1-7) were abolished by the Ang-(1-7) receptor antagonist A-799. Ang II treatment caused activation of ERK1/2 mediated signaling, and this was inhibited by preincubation of SMCs with Ang-(1-7).
These results suggest that Ang-(1-7) inhibits Ang II-induced SMC proliferation and migration, at least in part, through negative modulation of Ang II induced ERK1/2 activity.
血管紧张素(Ang)II 和 Ang-(1-7) 是肾素-血管紧张素系统的两种生物活性肽。Ang II 参与心血管疾病的发展,如高血压和动脉粥样硬化,而 Ang-(1-7) 与 Ang II 相反,具有心血管保护作用。
方法/主要发现:在这项研究中,我们研究了 Ang II 和 Ang-(1-7) 对血管平滑肌细胞(SMC)增殖和迁移的影响,这在动脉粥样硬化病变的形成中至关重要。用 Ang II 处理会导致 SMC 增殖增加,而 Ang-(1-7) 单独使用则没有影响。然而,Ang-(1-7) 的预先孵育抑制了 Ang II 诱导的 SMC 增殖。Ang II 促进 SMC 迁移,而 Ang-(1-7) 的预处理则消除了这种作用。Ang II 受体拮抗剂洛沙坦阻断了 Ang II 对 SMC 增殖和迁移的刺激作用,而 Ang-(1-7) 受体拮抗剂 A-799 则消除了 Ang-(1-7) 的抑制作用。Ang II 处理导致 ERK1/2 介导的信号转导激活,而 SMC 用 Ang-(1-7) 预先孵育则抑制了这种激活。
这些结果表明,Ang-(1-7) 通过负向调节 Ang II 诱导的 ERK1/2 活性,至少部分抑制 Ang II 诱导的 SMC 增殖和迁移。