Cathepsin cysteine proteases in cardiovascular disease

被引:242
作者
Lutgens, Suzanne P. M. [1 ]
Cleutjens, Kitty B. J. M. [1 ]
Daemen, Mat J. A. P. [1 ]
Heeneman, Sylvia [1 ]
机构
[1] Maastricht Univ, CARIM, Dept Pathol, NL-6200 MD Maastricht, Netherlands
关键词
atherosclerosis; extracellular matrix; lipid metabolism; diagnostic tool; therapeutic potential;
D O I
10.1096/fj.06-7924com
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
Extracellular matrix (ECM) remodeling is one of the underlying mechanisms in cardiovascular diseases. Cathepsin cysteine proteases have a central role in ECM remodeling and have been implicated in the development and progression of cardiovascular diseases. Cathepsins also show differential expression in various stages of atherosclerosis, and in vivo knockout studies revealed that deficiency of cathepsin K or S reduces atherosclerosis. Furthermore, cathepsins are involved in lipid metabolism. Cathepsins have the capability to degrade low-density lipoprotein and reduce cholesterol efflux from macrophages, aggravating foam cell formation. Although expression studies also demonstrated differential expression of cathepsins in cardiovascular diseases like aneurysm formation, neointima formation, and neovascularization, in vivo studies to define the exact role of cathepsins in these processes are lacking. Evaluation of the feasibility of cathepsins as a diagnostic tool revealed that serum levels of cathepsins L and S seem to be promising as biomarkers in the diagnosis of atherosclerosis, whereas cathepsin B shows potential as an imaging tool. Furthermore, cathepsin K and S inhibitors showed effectiveness in (pre) clinical evaluation for the treatment of osteoporosis and osteoarthritis, suggesting that cathepsin inhibitors may also have therapeutic effects for the treatment of atherosclerosis.
引用
收藏
页码:3029 / 3041
页数:13
相关论文
共 100 条
[1]  
Abbenante Giovanni, 2005, Med Chem, V1, P71, DOI 10.2174/1573406053402569
[2]   Risk factors for abdominal aortic aneurysms in older adults enrolled in the cardiovascular health study [J].
Alcorn, HG ;
Wolfson, SK ;
SuttonTyrrell, K ;
Kuller, LH ;
OLeary, D .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (08) :963-970
[3]   SPECIFICITY OF CATHEPSIN-B - HYDROLYSIS OF GLUCAGON AT C-TERMINUS BY A PEPTIDYL-DIPEPTIDASE MECHANISM [J].
ARONSON, NN ;
BARRETT, AJ .
BIOCHEMICAL JOURNAL, 1978, 171 (03) :759-765
[4]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[5]   Human cathepsin S, but not cathepsin L, degrades efficiently MHC class II-associated invariant chain in nonprofessional APCs [J].
Bania, J ;
Gatti, E ;
Lelouard, H ;
David, A ;
Cappello, F ;
Weber, E ;
Camosseto, V ;
Pierre, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6664-6669
[6]   Cathepsin S controls MHC class II-mediated antigen presentation by epithelial cells in vivo [J].
Beers, C ;
Burich, A ;
Kleijmeer, MJ ;
Griffith, JM ;
Wong, P ;
Rudensky, AY .
JOURNAL OF IMMUNOLOGY, 2005, 174 (03) :1205-1212
[7]   Differential regulation of cathepsin S and cathepsin L in interferon γ-treated macrophages [J].
Beers, C ;
Honey, K ;
Fink, S ;
Forbush, K ;
Rudensky, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (02) :169-179
[8]   Lack of the cysteine protease inhibitor cystatin C promotes atherosclerosis in apolipoprotein E-deficient mice [J].
Bengtsson, E ;
To, F ;
Håkansson, K ;
Grubb, A ;
Brånén, L ;
Nilsson, J ;
Jovinge, S .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2151-2156
[9]   Human cathepsin O-2, a matrix protein-degrading cysteine protease expressed in osteoclasts - Functional expression of human cathepsin O-2 in Spodoptera frugiperda and characterization of the enzyme [J].
Bromme, D ;
Okamoto, K ;
Wang, BB ;
Biroc, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (04) :2126-2132
[10]   Cathepsin S expression is up-regulated following balloon angioplasty in the hypercholesterolemic rabbit [J].
Burns-Kurtis, CL ;
Olzinski, AR ;
Needle, S ;
Fox, JH ;
Capper, EA ;
Kelly, FM ;
McQueney, MS ;
Romanic, AM .
CARDIOVASCULAR RESEARCH, 2004, 62 (03) :610-620