ACTIVATED PLATELETS INDUCE SUPEROXIDE ANION RELEASE BY MONOCYTES AND NEUTROPHILS THROUGH P-SELECTIN (CD62)

被引:0
|
作者
NAGATA, K
TSUJI, T
TODOROKI, N
KATAGIRI, Y
TANOUE, K
YAMAZAKI, H
HANAI, N
IRIMURA, T
机构
[1] UNIV TOKYO,FAC PHARMACEUT SCI,DIV CHEM TOXICOL & IMMUNOCHEM,7-3-1 HONGO,BUNKYO KU,TOKYO 113,JAPAN
[2] TOKYO METROPOLITAN INST MED SCI,DEPT CARDIOVASC RES,TOKYO 113,JAPAN
[3] KYOWA HAKKO KOGYO CO LTD,TOKYO RES LABS,MACHIDA 194,JAPAN
来源
JOURNAL OF IMMUNOLOGY | 1993年 / 151卷 / 06期
关键词
D O I
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中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activated platelets expressing P-selectin on their surfaces are known to adhere to monocytes and neutrophils. We examined the possibility that the leukocytes are functionally modified by their adhesion to activated platelets. We used human peripheral blood monocytes and neutrophils and measured superoxide anion generation by these cells cultured with platelets. The levels of superoxide anion production were found to be markedly elevated when thrombin-activated platelets were used. The extent of this enhancement was much smaller when leukocytes were cultured with resting platelets than activated platelets. The increase depended on incubation time and platelet concentration. The membranes prepared from activated platelets also induced superoxide anion production, but the culture supernatant of activated platelets did not. The enhanced superoxide anion production was inhibited by anti-P-selectin antibody, anti-sialyl-Lewis X antibody, or a soluble recombinant P-selectin fusion protein. These results indicate that the adhesion of activated platelets to the leukocytes through P-selectin was a crucial step for the activation of leukocyte function, and support the idea that activated platelets are actively involved in inflammation processes.
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页码:3267 / 3273
页数:7
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