Transcriptional regulation of matrix metalloprotease gene expression in health and disease

被引:38
作者
Mancini, A [1 ]
Di Battista, JA [1 ]
机构
[1] McGill Univ, Royal Victoria Hosp, Div Clin Immunol & Rheumatol, Montreal, PQ H3A 1A1, Canada
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
matrix metalloprotease; MMPs; transcriptional regulation; promoter; arthritis; bone development; brain; cardiovascular; cancer; review;
D O I
10.2741/1809
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
The mammalian extracellular matrix (ECM) is a complex network of collagens, proteoglycans, glycoproteins, polysaccharides and other secreted proteins that plays fundamental structural and functional roles. In addition to its key function as an extracellular space-filling scaffold, the ECM is also implicated in the formation of important cell-cell and cell-ECM (i. e. juxtacrine) interactions that subsequently provide key regulatory signals that influence cellular proliferation and viability, differentiation, specialization and gene expression. Regulated turnover of the ECM, a process largely mediated by the tightly controlled matrix metalloprotease (MMP) enzyme family, is critical to a number of physiological processes involved in growth and development while aberrant turnover of matrix components is associated with congenital and metabolic diseases. The following review will focus on the transcriptional aspects of MMP gene expression, particularly in diseased states.
引用
收藏
页码:423 / 446
页数:24
相关论文
共 226 条
[71]  
Hayashita-Kinoh H, 2001, CELL GROWTH DIFFER, V12, P573
[72]  
HE QW, 2001, OSTEOARTHRITIS CAR B, V9, pS9
[73]  
He W, 2002, J RHEUMATOL, V29, P546
[74]   NF-κB p105 is a target of IκB kinases and controls signal induction of Bcl-3-p50 complexes [J].
Heissmeyer, V ;
Krappmann, D ;
Wulczyn, FG ;
Scheidereit, C .
EMBO JOURNAL, 1999, 18 (17) :4766-4778
[75]  
Henney AM, 2000, ANN NY ACAD SCI, V902, P27
[76]   AP-1 and Cbfa/runt physically interact and regulate parathyroid hormone-dependent MMP13 expression in osteoblasts through a new osteoblast-specific element 2/AP-1 composite element [J].
Hess, J ;
Porte, D ;
Munz, C ;
Angel, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :20029-20038
[77]  
HIGASHINO F, 1995, ONCOGENE, V10, P1461
[78]   MT1-MMP: A tethered collagenase [J].
Holmbeck, K ;
Bianco, P ;
Yamada, S ;
Birkedal-Hansen, H .
JOURNAL OF CELLULAR PHYSIOLOGY, 2004, 200 (01) :11-19
[79]  
HONGWEI Q, 1999, J BIOL CHEM, V274, P29130
[80]   TARGETED DISRUPTION OF THE C-FOS GENE DEMONSTRATES C-FOS-DEPENDENT AND C-FOS-INDEPENDENT PATHWAYS FOR GENE-EXPRESSION STIMULATED BY GROWTH-FACTORS OR ONCOGENES [J].
HU, ED ;
MUELLER, E ;
OLIVIERO, S ;
PAPAIOANNOU, VE ;
JOHNSON, R ;
SPIEGELMAN, BM .
EMBO JOURNAL, 1994, 13 (13) :3094-3103