CXC-chemokines in coronary artery disease:: possible pathogenic role of interactions between oxidized low-density lipoprotein, platelets and peripheral blood mononuclear cells

被引:37
作者
Holm, T
Damas, JK
Holven, K
Nordoy, I
Brosstas, FR
Ueland, T
Währe, T
Kjekshus, J
Froland, SS
Eiken, HG
Solum, NO
Gullestad, L
Nenseter, M
Aukrust, P [1 ]
机构
[1] Natl Hosp Norway, Dept Med, Sect Clin Immunol & Infect Dis, N-0027 Oslo, Norway
[2] Natl Hosp Norway, Endocrinol Sect, N-0027 Oslo, Norway
[3] Natl Hosp Norway, MSD Cardiovasc Res Ctr, N-0027 Oslo, Norway
[4] Natl Hosp Norway, Lipid Clin, N-0027 Oslo, Norway
[5] Natl Hosp Norway, Internal Med Res Inst, N-0027 Oslo, Norway
[6] Natl Hosp Norway, Dept Cardiol, N-0027 Oslo, Norway
关键词
atherosclerosis; chemokines; leukocytes; lipids; platelets;
D O I
10.1046/j.1538-7836.2003.00065.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CXC-chemokines maybe involved in atherogenesis. Herein we examined the possible role of CXC-chemokines in the inflammatory interactions between oxidized (ox-) low-density lipoprotein (LDL), platelets and peripheral blood mononuclear cells (PBMC) in 15 patients with coronary artery disease (CAD) without 'traditional' risk factors and 15 carefully matched controls. Our main findings were: (a) ox-LDL stimulated the release of the CXC-chemokines interleukin (IL)-8, ENA-78 and GRO-alpha from PBMC, particularly in CAD. (b) In platelets, ox-LDL induced release of ENA-78 and, when combined with SFLLRN, also of GRO-alpha, with significantly higher response in CAD. (c) Platelet-rich plasma, especially when costimulated with ox-LDL, enhanced the release of IL-8 from PBMC, particularly in CAD patients. (d) Freshly isolated PBMC showed markedly increased IL-8 mRNA expression in CAD patients. Our findings suggest enhanced inflammatory interactions between ox-LDL, platelets and PBMC in CAD patients involving CXC-chemokine related mechanisms, possible contributing to atherogenesis in these and other CAD patients.
引用
收藏
页码:257 / 262
页数:6
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