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波形蛋白3(WAVE3)通过调节基质金属蛋白酶-1(MMP-1)、基质金属蛋白酶-3(MMP-3)和基质金属蛋白酶-9(MMP-9)的表达来促进细胞迁移和侵袭。

WAVE3 promotes cell motility and invasion through the regulation of MMP-1, MMP-3, and MMP-9 expression.

作者信息

Sossey-Alaoui Khalid, Ranalli Tamara A, Li Xiurong, Bakin Andrei V, Cowell John K

机构信息

Department of Cancer Genetics, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.

出版信息

Exp Cell Res. 2005 Aug 1;308(1):135-45. doi: 10.1016/j.yexcr.2005.04.011.

Abstract

WAVE3 is a member of the WASP/WAVE family of proteins, which play a critical role in the regulation of actin polymerization, cytoskeleton organization, and cell motility. We show here that knockdown of the WAVE3 protein, using RNA interference in MDA-MB-231 cells, decreases phospho-p38 MAPK levels, but not those of phospho-AKT, phospho-ERK, or phospho-JNK. Knockdown of WAVE3 expression also inhibited the expression levels of MMP-1, MMP-3, and MMP-9, but not MMP-2. MMP production could be restored by PMA treatment, without affecting siRNA-mediated WAVE3 knockdown. The WAVE3-mediated downregulation of p38 activity and MMP production is independent of the presence of both WAVE1 and WAVE2, whose expression levels were not affected by loss of WAVE3. We also show that the downstream effect of the WAVE3 knockdown is the inhibition of cell motility and invasion, coupled with increased actin stress fiber formation, as well as reorganization of focal adhesion complexes. These findings suggest that WAVE3 regulates actin cytoskeleton, cell motility, and invasion through the p38 MAPK pathway and MMP production.

摘要

WAVE3是WASP/WAVE蛋白家族的成员之一,该家族蛋白在肌动蛋白聚合、细胞骨架组织和细胞运动的调节中起关键作用。我们在此表明,在MDA-MB-231细胞中利用RNA干扰技术敲低WAVE3蛋白,可降低磷酸化p38 MAPK的水平,但不会降低磷酸化AKT、磷酸化ERK或磷酸化JNK的水平。敲低WAVE3的表达也会抑制MMP-1、MMP-3和MMP-9的表达水平,但不会影响MMP-2。PMA处理可恢复MMP的产生,且不影响siRNA介导的WAVE3敲低。WAVE3介导的p38活性下调和MMP产生与WAVE1和WAVE2的存在无关,WAVE1和WAVE2的表达水平不受WAVE3缺失的影响。我们还表明,WAVE3敲低的下游效应是抑制细胞运动和侵袭,同时增加肌动蛋白应力纤维的形成以及粘着斑复合物的重组。这些发现表明,WAVE3通过p38 MAPK途径和MMP产生来调节肌动蛋白细胞骨架、细胞运动和侵袭。

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