Electron microscopic examination of podosomes induced by phorbol 12, 13 dibutyrate on the surface of A7r5 cells

被引:6
|
作者
Tanaka, Hideyuki [1 ]
Wang, Hong-Hui [2 ,3 ]
Thatcher, Sean E. [4 ]
Hagiwara, Haruo [1 ]
Takano-Ohmuro, Hiromi [5 ]
Kohama, Kazuhiro [5 ]
机构
[1] Teikyo Univ, Sch Med, Dept Anat, Itabashi Ku, Tokyo 1738605, Japan
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Hunan Univ, Coll Biol, Changsha 410082, Hunan, Peoples R China
[4] Univ Kentucky, Dept Nutr Sci, Lexington, KY 40536 USA
[5] Musashino Univ, Pharmaceut Sci Res Inst, Nishitokyo, Tokyo 2028585, Japan
关键词
Podosome; Immunoelectron microscopy; Myosin light chain kinase; SMOOTH-MUSCLE-CELLS; LIGHT-CHAIN KINASE; LOCALIZATION; CONTRACTION; PROTEIN;
D O I
10.1016/j.jphs.2015.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The role of myosin light chain kinase (MLCK) in inducing podosomes was examined by confocal and electron microscopy. Removal of myosin from the actin core of podosomes using blebbistatin, a myosin inhibitor, resulted in the formation of smaller podosomes. Downregulation of MLCK by the transfection of MLCK small interfering RNA (siRNA) led to the failure of podosome formation. However, ML-7, an inhibitor of the kinase activity of MLCK, failed to inhibit podosome formation. Based on our previous report (Thatcher et al. J. Pharm. Sci. 116 116-127, 2011), we outlined the important role of the actin-binding activity of MLCK in producing smaller podosomes. (C) 2015 Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:78 / 82
页数:5
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