Down-Regulation of Myosin Light Chain Kinase Expression in Vascular Smooth Muscle Cells Accelerates Cell Proliferation: Requirement of Its Actin-binding Domain for Reversion to Normal Rates

被引:2
|
作者
Wang, Hong Hui [1 ]
Nakamura, Akio [1 ]
Yoshiyama, Shinji [1 ]
Ishikawa, Ryoki [1 ]
Cai, Na [2 ]
Ye, Li-Hong [2 ]
Takano-Ohmuro, Hiromi [3 ]
Kohama, Kazuhiro [1 ,3 ]
机构
[1] Gunma Univ, Grad Sch Med, Dept Mol & Cellular Pharmacol, Gunma 3718511, Japan
[2] Nankai Univ, Coll Life Sci, Dept Biochem, Tianjin 300071, Peoples R China
[3] Musashino Univ, Pharmaceut Sci Res Inst, Tokyo 2028585, Japan
关键词
myosin light-chain kinase; actin-binding domain; vascular smooth muscle proliferation; CONTRACTION; SPHINGOSYLPHOSPHORYLCHOLINE; LOCALIZATION; CYTOKINESIS; CALMODULIN; CULTURE;
D O I
10.1254/jphs.11213SC
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Myosin light-chain kinase (MLCK) is a multi-domain protein with kinase and actin-binding domains, among others. Deficiency of MLCK expression in GBaSM-4 vascular smooth muscle cells enhanced cell proliferation rate and shortened cell doubling time. Transient transfection of the MLCK-deficient cells with cDNA constructs of either wild-type MLCK or its mutant lacking the kinase activity reverted the cell proliferation rate to that of wild-type cells, whereas that of MLCK lacking the actin-binding domain maintained cell proliferation at an elevated rate similar to the MLCK-deficient cells. Thus, the actin-binding domain of MLCK seems to play a role in regulating cell proliferation.
引用
收藏
页码:91 / 96
页数:6
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