Tat-induced platelet-activating factor synthesis contributes to the angiogenic effect of HIV-1 Tat

被引:0
|
作者
Del Sorbo, L
Arese, M
Giraudo, E
Tizzani, M
Biancone, L
Bussolino, F
Camussi, G
机构
[1] Univ Turin, Dipartimento Med Interna, Lab Immunopatol Renale, I-10126 Turin, Italy
[2] Univ Turin, Dipartimento Genet Biol & Biochim, Turin, Italy
关键词
HIV-Tat; angiogenesis; platelet-activating factor;
D O I
10.1002/1521-4141(200102)31:2<376::AID-IMMU376>3.0.CO;2-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study shows that human umbilical cord vein-derived endothelial cells (HUVEC) stimulated with HIV-1 Tat synthesized platelet-activating factor (PAF), a phospholipid mediator of inflammation that possesses angiogenic properties. The synthesis of PAF by HUVEC stimulated with Tat was dose and time dependent. Moreover, in vitro experiments were performed to evaluate whether migration of HUVEC induced by Tat was dependent on the synthesis of PAF. It was found that the cell motility induced by Tat was inhibited by WEB 2170, a specific PAF receptor antagonist. In vivo, the neoangiogenesis induced by Tat was also inhibited by WEB 2170 in a murine model, in which matrigel subcutaneously injected was used as substratum for angiogenesis. These results suggest that the synthesis of PAF by endothelial cells mediates, at least in part, the angiogenic activity of Tat by promoting the endothelial cell migration.
引用
收藏
页码:376 / 383
页数:8
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