Extracellular proteases in atherosclerosis and restenosis

被引:128
作者
Garcia-Touchard, A
Henry, TD
Sangiorgi, G
Spagnoli, LG
Mauriello, A
Conover, C
Schwartz, RS
机构
[1] Minnesota Cardiovasc Res Inst, Minneapolis Heart Inst, Minneapolis, MN 55407 USA
[2] Univ Roma Tor Vergata, Div Anat Pathol, Rome, Italy
[3] Univ Roma Tor Vergata, Dept Cardiovasc Dis, Rome, Italy
[4] Mayo Clin & Mayo Fdn, Endocrine Res Unit, Rochester, MN 55905 USA
关键词
acute coronary syndromes; aneurysms; athersclerosis; proteases; restenosis;
D O I
10.1161/01.ATV.0000164311.48592.da
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Extracellular proteolysis plays a key role in many pathophysiologic processes including cancer, inflammatory diseases, and cardiovascular conditions such as atherosclerosis and restenosis. Whereas matrix metalloproteinases are their best known member, many others are becoming better known. The extracellular proteases are a complex and heterogeneous superfamily of enzymes. They include metalloproteinases ( matrix metalloproteinases, adamalysins, or pappalysins), serine proteases ( elastase, coagulation factors, plasmin, tissue plasminogen activator, urokinase plasminogen activator), and the cysteine proteases ( such cathepsins). In addition to their matrix degradation capabilities, they have other less well known biologic functions that include angiogenesis, growth factor bioavailability, cytokine modulation, receptor shedding, enhancing cell migration, proliferation, invasion, and apoptosis. This review discusses extracellular proteases relevant to the vasculature, their classification and function, and how protease disorders contribute to arterial plaque growth, including chronic atherosclerosis, acute coronary syndromes, restenosis, and vascular remodeling. These broad extracellular protease functions make them potentially interesting therapeutic targets.
引用
收藏
页码:1119 / 1127
页数:9
相关论文
共 99 条
[1]  
ABBOUD RT, 1986, J LAB CLIN MED, V108, P294
[2]   Cystatins [J].
Abrahamson, M ;
Alvarez-Fernandez, M ;
Nathanson, CM .
PROTEASES AND THE REGULATION OF BIOLOGICAL PROCESSES, 2003, 70 :179-199
[3]   Increased expression of disintegrin-metalloproteinases ADAM-15 and ADAM-9 following upregulation of integrins α5β1 and αvβ3 in atherosclerosis [J].
Al-Fakhri, N ;
Wilhelm, J ;
Hahn, M ;
Heidt, M ;
Hehrlein, FW ;
Endisch, AM ;
Hupp, T ;
Cherian, SM ;
Bobryshev, YV ;
Lord, RSA ;
Katz, N .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 89 (04) :808-823
[4]   Prevention of aneurysm development and rupture by local overexpression of plasminogen activator inhibitor-1 [J].
Allaire, E ;
Hasenstab, D ;
Kenagy, RD ;
Starcher, B ;
Clowes, MM ;
Clowes, AW .
CIRCULATION, 1998, 98 (03) :249-255
[5]  
Andreasen PA, 1997, INT J CANCER, V72, P1, DOI 10.1002/(SICI)1097-0215(19970703)72:1<1::AID-IJC1>3.0.CO
[6]  
2-Z
[7]   TRANSFORMING GROWTH-FACTOR-ALPHA AND BETA-AMYLOID PRECURSOR PROTEIN SHARE A SECRETORY MECHANISM [J].
ARRIBAS, J ;
MASSAGUE, J .
JOURNAL OF CELL BIOLOGY, 1995, 128 (03) :433-441
[8]   Metalloproteinase inhibitors: biological actions and therapeutic opportunities [J].
Baker, AH ;
Edwards, DR ;
Murphy, G .
JOURNAL OF CELL SCIENCE, 2002, 115 (19) :3719-3727
[9]   Divergent effects of tissue inhibitor of metalloproteinase-1, -2, or -3 overexpression on rat vascular smooth muscle cell invasion, proliferation, and death in vitro - TIMP-3 promotes apoptosis [J].
Baker, AH ;
Zaltsman, AB ;
George, SJ ;
Newby, AC .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1478-1487
[10]   Pregnancy-associated plasma protein a as a marker of acute coronary syndromes [J].
Bayes-Genis, A ;
Conover, CA ;
Overgaard, MT ;
Bailey, KR ;
Christiansen, M ;
Holmes, DR ;
Virmani, R ;
Oxvig, C ;
Schwartz, RS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (14) :1022-1029