MRP-1/CD9 gene transduction regulates the actin cytoskeleton through the downregulation of WAVE2

被引:18
作者
Huang, C-L
Ueno, M.
Liu, D.
Masuya, D.
Nakano, J.
Yokomise, H.
Nakagawa, T.
Miyake, M.
机构
[1] Kagawa Univ, Dept Surg 2, Fac Med, Kagawa 7610793, Japan
[2] Kagawa Univ, Fac Med, Dept Pathol & Host Def, Kagawa, Japan
[3] Kagawa Univ, Life Sci Res Ctr, Kagawa, Japan
[4] Kitano Hosp, Dept Oncol 5, Tazuke Kofukai Med Res Inst, Dept Thorac Surg, Osaka, Japan
关键词
MRP-1/CD9; WAVE2; actin; motility;
D O I
10.1038/sj.onc.1209654
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Motility-related protein-1 (MRP-1/CD9) is involved in cell motility. We studied the change in the actin cytoskeleton, and the expression of actin-related protein (Arp) 2 and Arp3 and the Wiskott-Aldrich syndrome protein ( WASP) family according to MRP-1/CD9 gene transduction into HT1080 cells. The frequency of cells with lamellipodia was significantly lower in MRP-1/CD9-transfected HT1080 cells than in control HT1080 cells (P < 0.0001). MRP-1/CD9 gene transduction affected the subcellular localization of Arp2 and Arp3 proteins. Furthermore, MRP-1/CD9 gene transduction induced a downregulation of WAVE2 expression (P < 0.0001). However, no difference was observed in the expression of Arp2, Arp3 or other WASPs. A neutralizing anti-MRP-1/CD9 monoclonal antibody inhibited downregulation of WAVE2 in MRP-1/CD9-transfected HT1080 cells (P < 0.0001 ), and reversed the morphological effects of MRP-1/CD9 gene transduction. Furthermore, downregulation of WAVE2 by transfection of WAVE2-specific small interfering RNA ( siRNA) mimicked the morphological effects of MRP-1/CD9 gene transduction and suppressed cell motility. However, transfection of each siRNA for Wnt1, Wnt2b1 or Wnt5a did not affect WAVE2 expression. Transfection of WAVE2-specific siRNA also did not affect expressions of these Wnts. These results indicate that MRP-1/CD9 regulates the actin cytoskeleton by downregulating of the WAVE2, through the Wnt-independent signal pathway.
引用
收藏
页码:6480 / 6488
页数:9
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