Journal of Leukocyte Biology Myeloid cells, immune suppression, tumor immunology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


A more recent version of this article appeared on July 1, 2005

Published online before print March 30, 2005
This Article
Right arrow Full Text (Reprint (PDF))
Right arrow All Versions of this Article:
jlb.0904498v1
78/1/259    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lu, Y.
Right arrow Articles by Wahl, L. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lu, Y.
Right arrow Articles by Wahl, L. M.
© by The Society for Leukocyte Biology
Journal of Leukocyte Biology, doi:10.1189/jlb.0904498


Received for publication September 7, 2004.
Revised February 1, 2005.
Accepted for publication March 7, 2005.


Article

Production of matrix metalloproteinase-9 by activated human monocytes involves a phosphatidylinositol-3 kinase/Akt/IKK{alpha}/NF-{kappa}B pathway

Yunbiao Lu and Larry M. Wahl @

Immunopathology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland

@ To whom correspondence should be addressed. E-mail: lwahl{at}dir.nidcr.nih.gov.


   Abstract

Matrix metalloproteinase-9 (MMP-9) is considered to be an important component in the progression of inflammation. Monocytes/macrophages are prominent at inflammation sites, and activation of these cells by stimulants, such as lipopolysaccharide (LPS) or tumor necrosis factor {alpha} and granulocyte macrophage-colony stimulating factor, leads to the production of significant amounts of MMP-9. Here, we show that LPS stimulation of monocytes results in MMP-9 production through a phosphatidylinositol-3 kinase (PI-3K)/Akt/inhibitor of {kappa}B (I{kappa}B) kinase-{alpha} (IKK{alpha})/nuclear factor (NF)-{kappa}B pathway. This new role for Akt in signaling leading to MMP-9 production was demonstrated by inhibitor and immunoprecipitation studies. LY294002 or wortmannin, inhibitors of PI-3K, suppressed LPS-induced Akt activity and MMP-9 production. Evidence for the participation of Akt in monocyte MMP-9 synthesis was demonstrated by the inhibition of MMP-9 by SH-5, a specific inhibitor of Akt. The mechanism by which Akt regulates MMP-9 is through the activation of NF-{kappa}B, as shown by coimmunoprecipitation of the phosphorylated form of IKK{alpha} and Akt as well as the SH-5 suppression of the dissociation of I{kappa}B from NF-{kappa}B and the activation of NF-{kappa}B p65. The role of NF-{kappa}B in regulation of MMP-9 was demonstrated further by the inhibition of MMP-9 production by proteasome inhibitors, lactacystin and MG-132, which prevented the ubiquitination and dissociation of I{kappa}B from NF-{kappa}B. This is the first demonstration that Akt is involved in the signaling pathway leading to the production of monocyte MMP-9 and provides an additional approach in the regulation of this enzyme in human primary monocytes.

Key Words: lipopolysaccharide • pleckstrin homology • PIP3




This article has been cited by other articles:


Home page
FASEB J.Home page
S. R. Perri, B. Annabi, and J. Galipeau
Angiostatin inhibits monocyte/macrophage migration via disruption of actin cytoskeleton
FASEB J, December 1, 2007; 21(14): 3928 - 3936.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
V. Gomez-Pina, A. Soares-Schanoski, A. Rodriguez-Rojas, C. del Fresno, F. Garcia, M. T. Vallejo-Cremades, I. Fernandez-Ruiz, F. Arnalich, P. Fuentes-Prior, and E. Lopez-Collazo
Metalloproteinases Shed TREM-1 Ectodomain from Lipopolysaccharide-Stimulated Human Monocytes
J. Immunol., September 15, 2007; 179(6): 4065 - 4073.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
C.-W. Lee, C.-C. Lin, W.-N. Lin, K.-C. Liang, S.-F. Luo, C.-B. Wu, S.-W. Wang, and C.-M. Yang
TNF-{alpha} induces MMP-9 expression via activation of Src/EGFR, PDGFR/PI3K/Akt cascade and promotion of NF-{kappa}B/p300 binding in human tracheal smooth muscle cells
Am J Physiol Lung Cell Mol Physiol, March 1, 2007; 292(3): L799 - L812.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
S. De Barros, A. Zakaroff-Girard, M. Lafontan, J. Galitzky, and V. Bourlier
Inhibition of Human Preadipocyte Proteasomal Activity by HIV Protease Inhibitors or Specific Inhibitor Lactacystin Leads to a Defect in Adipogenesis, Which Involves Matrix Metalloproteinase-9
J. Pharmacol. Exp. Ther., January 1, 2007; 320(1): 291 - 299.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
S.-S. Liau, A. Jazag, and E. E. Whang
HMGA1 Is a Determinant of Cellular Invasiveness and In vivo Metastatic Potential in Pancreatic Adenocarcinoma
Cancer Res., December 15, 2006; 66(24): 11613 - 11622.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
D. H. Li, J. W. Tung, I. H. Tarner, A. L. Snow, T. Yukinari, R. Ngernmaneepothong, O. M. Martinez, and J. R. Parnes
CD72 Down-Modulates BCR-Induced Signal Transduction and Diminishes Survival in Primary Mature B Lymphocytes
J. Immunol., May 1, 2006; 176(9): 5321 - 5328.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2005 by the Society for Leukocyte Biology.