Min Li-Juan, Mogi Masaki, Li Jian-Mei, Iwanami Jun, Iwai Masaru, Horiuchi Masatsugu
Division of Medical Biochemistry and Cardiovascular Biology, Department of Molecular and Cellular Biology, Ehime University School of Medicine, Tohon, Ehime 791-0295, Japan.
Circ Res. 2005 Sep 2;97(5):434-42. doi: 10.1161/01.RES.0000180753.63183.95. Epub 2005 Aug 4.
Interaction between aldosterone (Aldo) and angiotensin II (Ang II) in the cardiovascular system has been highlighted; however, its detailed signaling mechanism is poorly understood. Here, we examined the cross-talk of growth-promoting signaling between Aldo and Ang II in vascular smooth muscle cells (VSMC). Treatment with a lower dose of Aldo (10(-12) mol/L) and with a lower dose of Ang II (10(-10) mol/L) significantly enhanced DNA synthesis, whereas Aldo or Ang II alone at these doses did not affect VSMC proliferation. This effect of a combination of Aldo and Ang II was markedly inhibited by a selective AT1 receptor blocker, olmesartan, a mineralocorticoid receptor antagonist, spironolactone, an MEK inhibitor, PD98059, or an EGF receptor tyrosine kinase inhibitor, AG1478. Treatment with Aldo together with Ang II, even at noneffective doses, respectively, synergistically increased extracellular signal-regulated kinase (ERK) activation, reaching 2 peaks at 10 to 15 minutes and 2 to 4 hours. The early ERK peak was effectively blocked by olmesartan or an EGF receptor kinase inhibitor, AG1478, but not by spironolactone, whereas the late ERK peak was completely inhibited by not only olmesartan, but also spironolactone. Combined treatment with Aldo and Ang II attenuated mitogen-activated protein kinase phosphatase-1 (MKP-1) expression and increased Ki-ras2A expression. The late ERK peak was not observed in VSMC treated with Ki-ras2A-siRNA. Interestingly, the decrease in MKP-1 expression and the increase in Ki-ras2A expression were restored by PD98059 or AG1478. These results suggest that Aldo exerts a synergistic mitogenic effect with Ang II and support the notion that blockade of both Aldo and Ang II could be more effective to prevent vascular remodeling.
醛固酮(Aldo)与血管紧张素II(Ang II)在心血管系统中的相互作用已受到关注;然而,其详细的信号传导机制仍知之甚少。在此,我们研究了醛固酮与血管紧张素II在血管平滑肌细胞(VSMC)中促进生长信号的相互作用。用较低剂量的醛固酮(10^(-12) mol/L)和较低剂量的血管紧张素II(10^(-10) mol/L)处理可显著增强DNA合成,而单独使用这些剂量的醛固酮或血管紧张素II并不影响VSMC增殖。醛固酮与血管紧张素II联合使用的这种作用被选择性AT1受体阻滞剂奥美沙坦、盐皮质激素受体拮抗剂螺内酯、MEK抑制剂PD98059或表皮生长因子受体酪氨酸激酶抑制剂AG1478显著抑制。即使分别使用无效剂量的醛固酮和血管紧张素II共同处理,也能协同增加细胞外信号调节激酶(ERK)的激活,在10至15分钟和2至4小时达到两个峰值。早期ERK峰值被奥美沙坦或表皮生长因子受体激酶抑制剂AG1478有效阻断,但不被螺内酯阻断,而晚期ERK峰值不仅被奥美沙坦完全抑制,也被螺内酯完全抑制。醛固酮与血管紧张素II联合处理可减弱丝裂原活化蛋白激酶磷酸酶-1(MKP-1)的表达并增加Ki-ras2A的表达。在用Ki-ras2A-siRNA处理的VSMC中未观察到晚期ERK峰值。有趣的是,PD98059或AG1478可恢复MKP-1表达的降低和Ki-ras2A表达的增加。这些结果表明,醛固酮与血管紧张素II发挥协同促有丝分裂作用,并支持这样一种观点,即同时阻断醛固酮和血管紧张素II可能对预防血管重塑更有效。