Nagumo H, Sasaki Y, Ono Y, Okamoto H, Seto M, Takuwa Y
Departments of Molecular and Cellular Physiology and Cardiovascular Biology, University of Tokyo School of Medicine, Tokyo 113-0033, Japan.
Am J Physiol Cell Physiol. 2000 Jan;278(1):C57-65. doi: 10.1152/ajpcell.2000.278.1.C57.
In smooth muscle, a Rho-regulated system of myosin phosphatase exists; however, it has yet to be established whether Rho kinase, one of the downstream effectors of Rho, mediates the regulation of myosin phosphatase activity in vivo. In the present study, we demonstrate in permeabilized vascular smooth muscle cells (SMCs) that the vasodilator 1-(5-isoquinolinesulfonyl)-homopiperazine (HA-1077), which we show to be a potent inhibitor of Rho kinase, dose dependently inhibits Rho-mediated enhancement of Ca(2+)-induced 20-kDa myosin light chain (MLC(20)) phosphorylation due to abrogating Rho-mediated inhibition of MLC(20) dephosphorylation. By an immune complex phosphatase assay, we found that guanosine 5'-O-(3-thiotriphosphate) (GTPgammaS) stimulation of permeabilized SMCs caused a decrease in myosin phosphatase activity with an increase in the extent of phosphorylation of the 130-kDa myosin-binding regulatory subunit (MBS) of myosin phosphatase in a Rho-dependent manner. HA-1077 abolished both of the Rho-mediated events. Moreover, we observed that the pleckstrin homology/cystein-rich domain protein of Rho kinase, a dominant negative inhibitor of Rho kinase, inhibited GTPgammaS-induced phosphorylation of MBS. These results provide direct in vivo evidence that Rho kinase mediates inhibition of myosin phosphatase activity with resultant enhancement of MLC(20) phosphorylation in smooth muscle and reveal the usefulness of HA-1077 as a Rho kinase inhibitor.
在平滑肌中,存在一种由Rho调节的肌球蛋白磷酸酶系统;然而,Rho的下游效应器之一Rho激酶是否在体内介导肌球蛋白磷酸酶活性的调节尚未确定。在本研究中,我们在通透的血管平滑肌细胞(SMC)中证明,血管舒张剂1-(5-异喹啉磺酰基)-高哌嗪(HA-1077),我们发现它是Rho激酶的有效抑制剂,由于消除了Rho介导的对20-kDa肌球蛋白轻链(MLC(20))去磷酸化的抑制作用,剂量依赖性地抑制了Rho介导的Ca(2+)诱导的MLC(20)磷酸化增强。通过免疫复合物磷酸酶测定,我们发现用鸟苷5'-O-(3-硫代三磷酸)(GTPγS)刺激通透的SMC会导致肌球蛋白磷酸酶活性降低,同时肌球蛋白磷酸酶的130-kDa肌球蛋白结合调节亚基(MBS)的磷酸化程度以Rho依赖的方式增加。HA-1077消除了这两个Rho介导的事件。此外,我们观察到Rho激酶的普列克底物蛋白同源性/富含半胱氨酸结构域蛋白,一种Rho激酶的显性负性抑制剂,抑制了GTPγS诱导的MBS磷酸化。这些结果提供了直接的体内证据,表明Rho激酶介导对肌球蛋白磷酸酶活性的抑制,从而导致平滑肌中MLC(20)磷酸化增强,并揭示了HA-1077作为Rho激酶抑制剂的用途。