A new role for cortactin in invadopodia: Regulation of protease secretion

被引:130
作者
Clark, Emily S. [1 ]
Weaver, Alissa M. [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Canc Biol, Nashville, TN 37232 USA
关键词
cortactin; invadopodia; matrix metalloproteinase; protease; membrane trafficking; vesicle;
D O I
10.1016/j.ejcb.2008.01.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Invadopodia are actin-dependent organelles that function in the invasion and remodeling of the extracellular matrix (ECM) by tumor cells. Cortactin, a regulator of the Arp2/3 complex, is of particular importance in invadopodia function. While most of the focus has been on the possible role of cortactin in actin assembly for direct formation of actin-rich invadopodia puncta, our recent data suggest that the primary role of cortactin in invadopodia is to promote protease secretion. In this manuscript, we review our previous work and present new data showing that cortactin is essential for both the localization of key invadopodia matrix metalloproteinases (MMPs) to actin-positive puncta at the cell-ECM interface and for ECM degradation induced by overexpression of MTI-MMP-GFP. Based on these data and results from the literature. we propose potential mechanisms by which cortactin may link vesicular trafficking and dynamic branched actin assembly to regulate protease secretion for invadopodia-associated ECM degradation. (C) 2008 Elsevier GmbH. All rights reserved.
引用
收藏
页码:581 / 590
页数:10
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