Wang Yu, Yoshioka Kazuaki, Azam Mohammed Ali, Takuwa Noriko, Sakurada Sotaro, Kayaba Yuji, Sugimoto Naotoshi, Inoki Isao, Kimura Takaharu, Kuwaki Tomoyuki, Takuwa Yoh
Department of Physiology, Kanazawa University Graduate School of Medicine, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.
Biochem J. 2006 Mar 15;394(Pt 3):581-92. doi: 10.1042/BJ20051471.
We demonstrated previously that membrane depolarization and excitatory receptor agonists such as noradrenaline induce Ca2+-dependent Rho activation in VSM (vascular smooth muscle), resulting in MP (myosin phosphatase) inhibition through the mechanisms involving Rho kinase-mediated phosphorylation of its regulatory subunit MYPT1. In the present study, we show in de-endothelialized VSM strips that the PI3K (phosphoinositide 3-kinase) inhibitors LY294002 and wortmannin inhibited KCl membrane depolarization- and noradrenaline-induced Rho activation and MYPT1 phosphorylation, with concomitant inhibition of MLC (20-kDa myosin light chain) phosphorylation and contraction. LY294002 also augmented de-phosphorylation of MLC and resultantly relaxation in KCl-contracted VSM, whereas LY294002 was much less effective or ineffective under the conditions in which MP was inhibited by either a phosphatase inhibitor or a phorbol ester in Rho-independent manners. VSM express at least four PI3K isoforms, including the class I enzymes p110alpha and p110beta and the class II enzymes PI3K-C2alpha and -C2beta. The dose-response relationships of PI3K-inhibitor-induced inhibition of Rho, MLC phosphorylation and contraction were similar to that of PI3K-C2alpha inhibition, but not to that of the class I PI3K inhibition. Moreover, KCl and noradrenaline induced stimulation of PI3K-C2alpha in a Ca2+-dependent manner, but not of p110alpha or p110beta. Down-regulation of PI3K-C2alpha expression by siRNA (small interfering RNA) inhibited contraction and phosphorylation of MYPT1 and MLC in VSM cells. Finally, intravenous wortmannin infusion induced sustained hypotension in rats, with inhibition of PI3K-C2alpha activity, GTP-loading of Rho and MYPT1 phosphorylation in the artery. These results indicate the novel role of PI3K-C2alpha in Ca2+-dependent Rho-mediated negative control of MP and thus VSM contraction.
我们之前证明,膜去极化以及去甲肾上腺素等兴奋性受体激动剂可在血管平滑肌(VSM)中诱导Ca2+依赖性的Rho激活,通过涉及Rho激酶介导的其调节亚基MYPT1磷酸化的机制导致肌球蛋白磷酸酶(MP)抑制。在本研究中,我们在去内皮的VSM条带上发现,PI3K(磷脂酰肌醇3激酶)抑制剂LY294002和渥曼青霉素抑制KCl膜去极化以及去甲肾上腺素诱导的Rho激活和MYPT1磷酸化,同时抑制20 kDa肌球蛋白轻链(MLC)磷酸化和收缩。LY294002还增强了MLC的去磷酸化,并因此导致KCl收缩的VSM舒张,而在MP以不依赖Rho的方式被磷酸酶抑制剂或佛波酯抑制的条件下,LY294002的效果要弱得多或无效。VSM至少表达四种PI3K亚型,包括I类酶p110α和p110β以及II类酶PI3K-C2α和-C2β。PI3K抑制剂诱导的对Rho、MLC磷酸化和收缩的抑制的剂量反应关系与PI3K-C2α抑制的相似,但与I类PI3K抑制的不同。此外,KCl和去甲肾上腺素以Ca2+依赖性方式刺激PI3K-C2α,但不刺激p110α或p110β。通过小干扰RNA(siRNA)下调PI3K-C2α表达可抑制VSM细胞中MYPT1和MLC的收缩及磷酸化。最后,静脉内注入渥曼青霉素可导致大鼠持续低血压,同时抑制动脉中PI3K-C2α活性、Rho的GTP负载以及MYPT1磷酸化。这些结果表明PI3K-C2α在Ca2+依赖性Rho介导的对MP从而对VSM收缩的负性调控中具有新作用。