THE BINDING-SITE ON ICAM-1 FOR PLASMODIUM-FALCIPARUM INFECTED ERYTHROCYTES OVERLAPS, BUT IS DISTINCT FROM, THE LFA-1-BINDING SITE

被引:244
作者
BERENDT, AR
MCDOWALL, A
CRAIG, AG
BATES, PA
STERNBERG, MJE
MARSH, K
NEWBOLD, CI
HOGG, N
机构
[1] IMPERIAL CANC RES FUND, MACROPHAGE LAB, LONDON WC2A 3PX, ENGLAND
[2] IMPERIAL CANC RES FUND, BIOMOLEC MODELLING LAB, LONDON WC2A 3PX, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0092-8674(92)90207-S
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The intercellular adhesion molecule-1 (ICAM-1, CD54) is one of three putative endothelial receptors that mediate in vitro cytoadherence of P. falciparum-infected erythrocytes. Since cytoadherence to postcapillary venular endothelium is thought to be a major factor in the virulence of P. falciparum malaria, we have examined the interaction between ICAM-1 and the P. falciparum-infected cell, and have compared it with the interaction to the physiological counter receptor, the leukocyte integrin LFA-1. Our results demonstrate that the malaria-binding site resides in the first two domains of the ICAM-1 molecule and overlaps, but is distinct from, the LFA-1 site.
引用
收藏
页码:71 / 81
页数:11
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