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First published online 5 January 2010
doi: 10.1242/jcs.052167

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Dynamic regulation of ROCK in tumor cells controls CXCR4-driven adhesion events

¹ Departments of Oral Biology and Pharmacology, LSU Health Sciences Center, New Orleans, LA, 70112, USA
² Department of Medicine, Tulane University Medical Center, New Orleans, LA 70112, USA

^* Author for correspondence (bworth{at}lsuhsc.edu)

Accepted 2 November 2009

CXCR4 is a chemokine receptor often found aberrantly expressed on metastatic tumor cells. To investigate CXCR4 signaling in tumor cell adhesion, we stably overexpressed CXCR4 in MCF7 breast tumor cells. Cell attachment assays demonstrate that stimulation of the receptor with its ligand, CXCL12, promotes adhesion of MCF7-CXCR4 cells to both extracellular matrix and endothelial ligands. To more closely mimic the conditions experienced by a circulating tumor cell, we performed the attachment assays under shear stress conditions. We found that CXCL12-induced tumor cell attachment is much more pronounced under flow. ROCK is a serine/threonine kinase associated with adhesion and metastasis, which is regulated by CXCR4 signaling. Thus, we investigated the contribution of ROCK activity during CXC12-induced adhesion events. Our results demonstrate a biphasic regulation of ROCK in response to adhesion. During the initial attachment, inhibition of ROCK activity is required. Subsequently, re-activation of ROCK activity is required for maturation of adhesion complexes and enhanced tumor cell migration. Interestingly, CXCL12 partially reduces the level of ROCK activity generated by attachment, which supports a model in which stimulation with CXCL12 regulates tumor cell adhesion events by providing an optimal level of ROCK activity for effective migration.

Key words: CXCL12, CXCR4, ROCK, Flow, Metastasis, Tumor recruitment

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