INVOLVEMENT OF PLATELET ENDOTHELIAL-CELL ADHESION MOLECULE-1 IN NEUTROPHIL RECRUITMENT IN-VIVO

被引:419
作者
VAPORCIYAN, AA
DELISSER, HM
YAN, HC
MENDIGUREN, II
THOM, SR
JONES, ML
WARD, PA
ALBELDA, SM
机构
[1] UNIV PENN,MED CTR,DEPT MED,DIV PULM & CRIT CARE,PHILADELPHIA,PA 19104
[2] WISTAR INST ANAT & BIOL,PHILADELPHIA,PA 19104
[3] UNIV MICHIGAN,SCH MED,DEPT PATHOL,ANN ARBOR,MI 48109
[4] UNIV PENN,MED CTR,INST ENVIRONM MED,PHILADELPHIA,PA 19104
关键词
D O I
10.1126/science.8248808
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
During inflammation, neutrophils migrate from the vascular lumen into extravascular sites. In vitro assays have suggested that platelet-endothelial cell adhesion molecule-1 [PECAM-1 (CD31)], a member of the immunoglobulin superfamily, is required for the transmigration of neutrophils across endothelial monolayers. Antibody to human PECAM-1, which cross-reacts with rat PECAM-1, was found to block not only in vivo accumulation of rat neutrophils into the peritoneal cavity and the alveolar compartment of the lung but also neutrophil accumulation in human skin grafts transplanted onto immunodeficient mice. On the basis of these findings in three different models of inflammation, it appears that PECAM-1 is required for neutrophil transmigration in vivo and may thus be a potential therapeutic target.
引用
收藏
页码:1580 / 1582
页数:3
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