The Neuroscience Research Partnership, A-STAR, Singapore, Singapore.
FEBS Lett. 2011 May 6;585(9):1260-8. doi: 10.1016/j.febslet.2011.03.054. Epub 2011 Mar 30.
Cell movement requires forces generated by non-muscle myosin II (NM II) for coordinated protrusion and retraction. The Cdc42/Rac effector MRCK regulates a specific actomyosin network in the lamella essential for cell protrusion and migration. Together with the Rho effector ROK required for cell rear retraction, they cooperatively regulate cell motility and tumour cell invasion. Despite the increasing importance of ROK inhibitors for both experimental and clinical purposes, there is a lack of specific inhibitors for other related kinases such as MRCK. Here, we report the identification of chelerythrine chloride as a specific MRCK inhibitor. Its ability to block cellular activity of MRCK resulted in the specific loss of NM II-associated MLC phosphorylation in the lamella, and the consequential suppression of cell migration.
细胞运动需要非肌肉肌球蛋白 II(NM II)产生的力来协调突起和缩回。CDC42/Rac 效应物 MRCK 调节板片中的特定肌动球蛋白网络,这对于细胞突起和迁移是必不可少的。与 Rho 效应物 ROK 一起,后者对于细胞后端的缩回是必需的,它们共同调节细胞运动和肿瘤细胞侵袭。尽管 ROK 抑制剂在实验和临床方面的重要性日益增加,但缺乏针对其他相关激酶(如 MRCK)的特异性抑制剂。在这里,我们报告鉴定出氯化白屈菜红碱(chelerythrine chloride)是一种特异性的 MRCK 抑制剂。它阻断 MRCK 细胞活性的能力导致板片中 NM II 相关 MLC 磷酸化的特异性丧失,并由此抑制细胞迁移。