Hyaluronan-mediated CD44 interaction with RhoGEF and Rho kinase promotes Grb2-associated binder-1 phosphorylation and phosphatidylinositol 3-kinase signaling leading to cytokine (Macrophage-Colony stimulating factor) production and breast tumor progression

被引:205
作者
Bourguignon, LYW
Singleton, PA
Zhu, HB
Diedrich, F
机构
[1] Univ Calif San Francisco, Dept Med, Endocrine Unit 111N, San Francisco, CA 94121 USA
[2] Vet Affairs Med Ctr, Endocrine Unit 111N, San Francisco, CA 94121 USA
关键词
ANKYRIN-BINDING DOMAIN; DOCKING PROTEIN GAB1; CELL-MIGRATION; GROWTH-FACTOR; PHOSPHOINOSITIDE; 3-KINASE; M-CSF; OSTEOCLAST DIFFERENTIATION; OSTEOPROTEGERIN-LIGAND; SURVIVAL PATHWAY; FOCAL ADHESIONS;
D O I
10.1074/jbc.M301885200
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
In this study we have examined CD44 ( a hyaluronan ( HA) receptor) interaction with a RhoA-specific guanine nucleotide exchange factor ( p115RhoGEF) in human metastatic breast tumor cells (MDA-MB-231 cell line). Immunoprecipitation and immunoblot analyses indicate that both CD44 and p115RhoGEF are expressed in MDA-MB-231 cells and that these two proteins are physically associated as a complex in vivo. The binding of HA to MDA-MB-231 cells stimulates p115RhoGEF-mediated RhoA signaling and Rho kinase (ROK) activity, which, in turn, increases serine/threonine phosphorylation of the adaptor protein, Gab-1 (Grb2-associated binder-1). Phosphorylated Gab-1 promotes PI 3-kinase recruitment to CD44v3. Subsequently, PI 3-kinase is activated (in particular, alpha, beta, gamma forms but not the delta form of the p110 catalytic subunit), AKT signaling occurs, the cytokine (macrophage-colony stimulating factor (M-CSF)) is produced, and tumor cell-specific phenotypes ( e. g. tumor cell growth, survival and invasion) are up-regulated. Our results also demonstrate that HA/CD44-mediated oncogenic events ( e. g. AKT activation, M-CSF production and breast tumor cell-specific phenotypes) can be effectively blocked by a PI 3-kinase inhibitor (LY294002). Finally, we have found that overexpression of a dominant-negative form of ROK ( by transfection of MBA-MD-231 cells with the Rho-binding domain cDNA of ROK) not only inhibits HA/CD44-mediated RhoA-ROK activation and Gab-1 phosphorylation but also downregulates oncogenic signaling events ( e. g. Gab-1.PI 3-kinase-CD44v3 association, PI 3-kinase-mediated AKT activation, and M-CSF production) and tumor cell behaviors ( e. g. cell growth, survival, and invasion). Taken together, these findings strongly suggest that CD44 interaction with p115RhoGEF and ROK plays a pivotal role in promoting Gab-1 phosphorylation leading to Gab-1 . PI 3-kinase membrane localization, AKT signaling, and cytokine (M-CSF) production during HA-mediated breast cancer progression.
引用
收藏
页码:29420 / 29434
页数:15
相关论文
共 84 条
[51]   The cell adhesion molecule, GP116, is a new CD44 variant (ex14/v10) involved in hyaluronic acid binding and endothelial cell proliferation [J].
Lokeshwar, VB ;
Iida, N ;
Bourguignon, LYW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (39) :23853-23864
[52]   Osteoprotegerin and osteoprotegerin-ligand balance: a new paradigm in bone metabolism providing new therapeutic targets [J].
Lories, RJU ;
Luyten, FP .
CLINICAL RHEUMATOLOGY, 2001, 20 (01) :3-9
[53]   Breast cancer increases osteoclastogenesis by secreting M-CSF and upregulating RANKL in stromal cells [J].
Mancino, AT ;
Klimberg, VS ;
Yamamoto, M ;
Manolagas, SC ;
Abe, E .
JOURNAL OF SURGICAL RESEARCH, 2001, 100 (01) :18-24
[54]   Rho-associated kinase, a novel serine threonine kinase, as a putative target for the small GTP binding protein Rho [J].
Matsui, T ;
Amano, M ;
Yamamoto, T ;
Chihara, K ;
Nakafuku, M ;
Ito, M ;
Nakano, T ;
Okawa, K ;
Iwamatsu, A ;
Kaibuchi, K .
EMBO JOURNAL, 1996, 15 (09) :2208-2216
[55]   Association of the multisubstrate docking protein Gab1 with the hepatocyte growth factor receptor requires a functional Grb2 binding site involving tyrosine 1356 [J].
Nguyen, L ;
HolgadoMadruga, M ;
Maroun, C ;
Fixman, ED ;
Kamikura, D ;
Fournier, T ;
Charest, A ;
Tremblay, ML ;
Wong, AJ ;
Park, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) :20811-20819
[56]   The role of phosphoinositide 3-kinase lipid products in cell function [J].
Rameh, LE ;
Cantley, LC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8347-8350
[57]   A novel positive feedback loop mediated by the docking protein Gab1 and phosphatidylinositol 3-kinase in epidermal growth factor receptor signaling [J].
Rodrigues, GA ;
Falasca, M ;
Zhang, ZT ;
Ong, SH ;
Schlessinger, J .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (04) :1448-1459
[58]  
RODRIGUEZVICIANA P, 1994, NATURE, V370, P527, DOI 10.1038/370527a0
[59]   Activation of phosphoinositide 3-kinase by interaction with Ras and by point mutation [J].
RodriguezViciana, P ;
Warne, PH ;
Vanhaesebroeck, B ;
Waterfield, MD ;
Downward, J .
EMBO JOURNAL, 1996, 15 (10) :2442-2451
[60]  
Rohrschneider LR, 1997, MOL REPROD DEV, V46, P96