Guanylate binding protein-1 inhibits spreading and migration of endothelial cells through induction of integrin α4 expression

被引:63
作者
Weinlaender, Kristina [1 ]
Naschberger, Elisabeth [1 ]
Lehmann, Michael H. [1 ]
Tripal, Philipp [1 ]
Paster, Wolfgang [2 ]
Stockinger, Hannes [2 ]
Hohenadl, Christine [3 ]
Stuerzl, Michael [1 ]
机构
[1] Univ Erlangen Nurnberg, Div Mol & Expt Surg, Dept Surg, D-91054 Erlangen, Germany
[2] Med Univ Vienna, Dept Mol Immunol, Ctr Physiol Pathophysiol & Immunol, Vienna, Austria
[3] Univ Vet Med, Dept Pathobiol, Inst Virol, Vienna, Austria
关键词
angiogenesis; inflammation; integrins; large GTPase;
D O I
10.1096/fj.08-107524
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
Human guanylate binding protein-1 (GBP-1) is a large GTPase that is induced by inflammatory cytokines and acts antiangiogenically through the inhibition of endothelial cell proliferation and migration. In this study, we detected that GBP-1-expressing cells show a significantly reduced spreading and migration on fibronectin matrices. Investigating possible mechanisms of these effects, we found that integrin alpha(4) (ITGA4) was consistently up-regulated at both the RNA and protein level in GBP-1-expressing cell cultures. Inhibition of cell spreading and migration by GBP-1 was dependent on the binding of ITGA4 to fibronectin. The inflammatory cytokines IL-1 beta and TNF-alpha induced ITGA4 expression in HUVECs and inhibited spreading and migration. Knockdown of GBP-1 by shRNA abrogated inflammatory cytokine induced ITGA4 expression and restored spreading and migration capabilities of the cells. These results show that inhibition of endothelial cell spreading and migration by inflammatory cytokines is mediated by GBP-1 through induction of ITGA4 expression. Endothelial cell migration is a key process during angiogenesis. Therefore, ITGA4 may be a novel molecular target to modulate angiogenesis in human disease.
引用
收藏
页码:4168 / 4178
页数:11
相关论文
共 75 条
[21]   Spatial restriction of α4 integrin phosphorylation regulates lamellipodial stability and α4β1-dependent cell migration [J].
Goldfinger, LE ;
Han, J ;
Kiosses, WB ;
Howe, AK ;
Ginsberg, MH .
JOURNAL OF CELL BIOLOGY, 2003, 162 (04) :731-741
[22]   The guanylate binding protein-1 GTPase controls the invasive and angiogenic capability of endothelial cells through inhibition of MMP-1 expression [J].
Guenzi, E ;
Töpolt, K ;
Lubeseder-Martellato, C ;
Jörg, A ;
Naschberger, E ;
Benelli, R ;
Albini, A ;
Stürzl, M .
EMBO JOURNAL, 2003, 22 (15) :3772-3782
[23]   The helical domain of GBP-1 mediates the inhibition of endothelial cell proliferation by inflammatory cytokines [J].
Guenzi, E ;
Töpolt, K ;
Cornali, E ;
Lubeseder-Martellato, C ;
Jörg, A ;
Matzen, K ;
Zietz, C ;
Kremmer, E ;
Nappi, F ;
Schwemmle, M ;
Hohenadl, C ;
Barillari, G ;
Tschachler, E ;
Monini, P ;
Ensoli, B ;
Stürzl, M .
EMBO JOURNAL, 2001, 20 (20) :5568-5577
[24]   Involvement of Rho GTPases in the transcriptional inhibition of preproendothelin-1 gene expression by simvastatin in vascular endothelial cells [J].
Hernández-Perera, O ;
Pérez-Sala, D ;
Soria, E ;
Lamas, S .
CIRCULATION RESEARCH, 2000, 87 (07) :616-622
[25]   THE RHO-FAMILY GTPASES RHOA, RAC1, AND CDC42HS REGULATE TRANSCRIPTIONAL ACTIVATION BY SRF [J].
HILL, CS ;
WYNNE, J ;
TREISMAN, R .
CELL, 1995, 81 (07) :1159-1170
[26]   INTEGRINS - VERSATILITY, MODULATION, AND SIGNALING IN CELL-ADHESION [J].
HYNES, RO .
CELL, 1992, 69 (01) :11-25
[27]   Integrins: Bidirectional, allosteric signaling machines [J].
Hynes, RO .
CELL, 2002, 110 (06) :673-687
[28]   ERBB-2 overexpression confers PI 3′ kinase-dependent invasion capacity on human mammary epithelial cells [J].
Ignatoski, KMW ;
Maehama, T ;
Markwart, SM ;
Dixon, JE ;
Livant, DL ;
Ethier, SP .
BRITISH JOURNAL OF CANCER, 2000, 82 (03) :666-674
[29]   Integrin fibronectin receptors in matrix metalloproteinase-1-dependent invasion by breast cancer and mammary epithelial cells [J].
Jia, YF ;
Zeng, ZZ ;
Markwart, SM ;
Rockwood, KF ;
Ignatoski, KMW ;
Ethier, SP ;
Livant, DL .
CANCER RESEARCH, 2004, 64 (23) :8674-8681
[30]   Integrins: roles in cancer development and as treatment targets [J].
Jin, H ;
Varner, J .
BRITISH JOURNAL OF CANCER, 2004, 90 (03) :561-565