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CD147 in Cardiovascular Disease and Thrombosis
被引:27
|作者:
Pennings, Gabrielle J.
[1
]
Kritharides, Leonard
[2
,3
,4
]
机构:
[1] Univ Sydney, Concord Repatriat Gen Hosp, ANZAC Res Inst, Vasc Biol Grp, Concord, NSW 2139, Australia
[2] Univ Sydney, ANZAC Res Inst, Atherosclerosis Grp, Concord, NSW 2139, Australia
[3] Univ Sydney, ANZAC Res Inst, Vasc Biol Grp, Concord, NSW 2139, Australia
[4] Concord Repatriat Gen Hosp, Dept Cardiol, Concord, NSW, Australia
来源:
关键词:
CD147;
EMMPRIN;
CAD;
thrombosis;
cyclophilin;
MATRIX-METALLOPROTEINASE INDUCER;
PLASMINOGEN-ACTIVATOR SYSTEM;
PLATELET GLYCOPROTEIN VI;
CORONARY-ARTERY-DISEASE;
IMMUNOGLOBULIN SUPERFAMILY;
HUMAN-FIBROBLASTS;
MESSENGER-RNA;
EMMPRIN CD147;
MOUSE BASIGIN;
CYCLOPHILIN;
D O I:
10.1055/s-0034-1390001
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Thrombotic and inflammatory pathways play a key role in coronary artery disease (CAD) development. Extracellular matrix metalloproteinase (aka CD147) is a member of the immunoglobulin superfamily that is expressed on many cell types including hematopoietic, endothelial cells, leukocytes, keratinocytes, platelets, and others. The binding partners of CD147 are numerous and diverse, and give some indication to the various roles that CD147 can play; these include homophilic interactions, integrins, cyclophilins, glycoprotein VI (GPVI), caveolin 1, and monocarboxylate transporters. Recent evidence suggests a role for CD147 in both thrombosis and inflammation, as well as involvement in CAD and cancer. In this review, we summarize the role of CD147 and its binding partners in platelets, thrombosis, and arterial disease and assess mechanistic aspects of CD147 biology.
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页码:747 / 755
页数:9
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