Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, CCS-bloco J, 21941-590 Rio de Janeiro, RJ, Brazil.
Arch Biochem Biophys. 2010 Apr 15;496(2):117-22. doi: 10.1016/j.abb.2010.02.005. Epub 2010 Feb 12.
We showed previously that angiotensin-(1-7) [Ang-(1-7)] reversed stimulation of proximal tubule Na+-ATPase promoted by angiotensin II (Ang II) through a D-ala(7)-Ang-(1-7) (A779)-sensitive receptor. Here we investigated the signaling pathway coupled to this receptor. According to our data, Ang-(1-7) produces a MAS-mediated reversal of Ang II-stimulated Na+-ATPase by a Gs/PKA pathway because: (1) the Ang-(1-7) effect is reversed by GDPbetaS, an inhibitor of trimeric G protein and Gs polyclonal antibody. Cholera toxin, an activator of Gs protein, mimicked it; (2) in the presence of Ang II, Ang-(1-7) increased the PKA activity 10-fold; (3) the peptide inhibitor of PKA blocked the Ang-(1-7) effect on Ang II-stimulated Na+-ATPase; (4) Ang-(1-7) reverses the Ang II-stimulated PKC activity; (5) cAMP mimicked the Ang-(1-7) effect on the Ang II-stimulated Na+-ATPase. Our results provide new understanding about the signaling mechanisms coupled to MAS receptor-mediated renal Ang-(1-7) effects.
我们之前已经表明,血管紧张素-(1-7)[血管紧张素-(1-7)] 通过 D-ala(7)-血管紧张素-(1-7)(A779)敏感受体逆转血管紧张素 II(Ang II)刺激近端肾小管 Na+-ATP 酶的作用。在这里,我们研究了与该受体偶联的信号通路。根据我们的数据,血管紧张素-(1-7) 通过 MAS 介导的 Gs/PKA 途径产生逆转 Ang II 刺激的 Na+-ATP 酶的作用,因为:(1) Ang-(1-7) 效应被 GDPβS 逆转,GDPβS 是三聚体 G 蛋白和 Gs 多克隆抗体的抑制剂。霍乱毒素是 Gs 蛋白的激活剂,模拟了它;(2) 在 Ang II 存在的情况下,Ang-(1-7) 使 PKA 活性增加 10 倍;(3) PKA 的肽抑制剂阻断 Ang-(1-7) 对 Ang II 刺激的 Na+-ATP 酶的作用;(4) Ang-(1-7) 逆转 Ang II 刺激的 PKC 活性;(5) cAMP 模拟了 Ang-(1-7) 对 Ang II 刺激的 Na+-ATP 酶的作用。我们的结果为 MAS 受体介导的肾脏 Ang-(1-7) 作用偶联的信号机制提供了新的认识。