Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2004
Published online before print November 4, 2004, doi: 10.1161/01.RES.0000150046.48115.80
A more recent version of this article appeared on November 26, 2004
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
95/11/1082    most recent
01.RES.0000150046.48115.80v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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 arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ray, B. K.
Right arrow Articles by Ray, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ray, B. K.
Right arrow Articles by Ray, A.
Related Collections
Right arrow Animal models of human disease
Right arrow Gene expression
Right arrow Gene regulation
Right arrow Mechanism of atherosclerosis/growth factors

Submitted on May 6, 2004
Revised on October 13, 2004
Accepted on October 26, 2004

Induction of the MMP-14 Gene in Macrophages of the Atherosclerotic Plaque. Role of SAF-1 in the Induction Process

Bimal K. Ray ; Arvind Shakya ; James R. Turk ; Suneel S. Apte ; and Alpana Ray *

From the Departments of Veterinary Pathobiology (B.K.R., A.S., A.R.) and Veterinary Biomedical Sciences (J.R.T.), University of Missouri, Columbia, Mo; and the Department of Biomedical Engineering (S.S.A.), Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio.

* To whom correspondence should be addressed. E-mail: rayal{at}missouri.edu.

Based on epidemiological and pathological studies, it is becoming increasingly clear that matrix metalloproteinases (MMPs) play an important role in the pathogenesis of atherosclerosis by participating in vascular remodeling, smooth muscle cell migration, and plaque disruption. MMP-14, because of its unique ability to cause pericellular degradation, its broad substrate specificity, its synthesis in an active form, and its ability to activate other matrix metalloproteinases, is recognized as a prominent member of this family. MMP-14 is detected at high levels in the atherosclerotic plaque. To understand the induction mechanism of MMP-14 under atherogenic conditions, we examined its expression pattern in response to oxidized low-density lipoproteins (ox-LDLs) that are believed to play an important role in atherogenesis. We report that in macrophages, ox-LDLs markedly elevate the levels of MMP-14 mRNA and protein. The cis-acting elements supporting this increase were identified to be present within -213 and -1 nucleotides of the MMP-14 promoter. DNase I protection assay revealed, within this region, two major elements, of which one serves as the DNA-binding site for SAF-1 transcription factor. Increased binding of SAF-1 to the MMP-14 promoter correlated with the transcriptional upregulation of MMP-14 gene. Furthermore, induction of endogenous MMP-14 gene, MMP-14 promoter driven reporter gene expression and MMP-2 processing activity during overexpression of SAF-1 and coexpression of SAF-1 and MMP-14 in the macrophages present in the atherosclerotic plaque implicate SAF-1 as a key regulator of MMP-14 gene induction in macrophage cells.


Key words: MMP-14 • SAF-1 • atherosclerotic plaques • oxidized LDL • macrophages




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
J. L. Johnson, G. B. Sala-Newby, Y. Ismail, C. M. Aguilera, and A. C. Newby
Low Tissue Inhibitor of Metalloproteinases 3 and High Matrix Metalloproteinase 14 Levels Defines a Subpopulation of Highly Invasive Foam-Cell Macrophages
Arterioscler Thromb Vasc Biol, September 1, 2008; 28(9): 1647 - 1653.
[Abstract] [Full Text] [PDF]


Home page
JEMHome page
J. R. Sierra, S. Corso, L. Caione, V. Cepero, P. Conrotto, A. Cignetti, W. Piacibello, A. Kumanogoh, H. Kikutani, P. M. Comoglio, et al.
Tumor angiogenesis and progression are enhanced by Sema4D produced by tumor-associated macrophages
J. Exp. Med., July 7, 2008; 205(7): 1673 - 1685.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
F. Schneider, G. K. Sukhova, M. Aikawa, J. Canner, N. Gerdes, S.-M. T. Tang, G.-P. Shi, S. S. Apte, and P. Libby
Matrix Metalloproteinase-14 Deficiency in Bone Marrow-Derived Cells Promotes Collagen Accumulation in Mouse Atherosclerotic Plaques
Circulation, February 19, 2008; 117(7): 931 - 939.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
B. K. Ray, A. Shakya, and A. Ray
Vascular Endothelial Growth Factor Expression in Arthritic Joint Is Regulated by SAF-1 Transcription Factor
J. Immunol., February 1, 2007; 178(3): 1774 - 1782.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
A. Ray, A. Shakya, D. Kumar, M. D. Benson, and B. K. Ray
Inflammation-Responsive Transcription Factor SAF-1 Activity Is Linked to the Development of Amyloid A Amyloidosis
J. Immunol., August 15, 2006; 177(4): 2601 - 2609.
[Abstract] [Full Text] [PDF]