INTERCELLULAR-ADHESION MOLECULE-2 (CD102) BINDS TO THE LEUKOCYTE INTEGRIN CD11B/CD18 THROUGH THE A-DOMAIN

被引:0
|
作者
XIE, JL
LI, R
KOTOVUORI, P
VERMOTDESROCHES, C
WIJDENES, J
ARNAOUT, MA
NORTAMO, P
GAHMBERG, CG
机构
[1] HELSINKI UNIV, DEPT BIOSCI, DIV BIOCHEM, SF-00014 HELSINKI, FINLAND
[2] MASSACHUSETTS GEN HOSP, DEPT MED, LEUKOCYTE BIOL & INFLAMMAT PROGRAM, BOSTON, MA 02114 USA
[3] HARVARD UNIV, SCH MED, BOSTON, MA 02114 USA
来源
JOURNAL OF IMMUNOLOGY | 1995年 / 155卷 / 07期
关键词
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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
The interactions between the leukocyte-specific beta 2-integrins cluster of differentiation (CD) Ag CD11/CD18 and their ligands, the intercellular adhesion molecules (ICAMs), play important roles in many adhesion-dependent leukocyte functions. ICAM-1 is known to be a ligand for both CD11a/CD18 and CD11b/CD18. ICAM-2, whose two extracellular Ig domains show the highest homology to the two NH2-terminal domains of ICAM-1, has been previously shown to be a ligand for CD11a/CD18. We recently found that a 22-amino acid CD11a/CD18-binding peptide, P1, derived from the first domain of ICAM-2, also binds to purified CD11b/CD18. In the present study, we demonstrate that the ICAM-2 protein interacts with CD11b/CD18, and the binding is through the CD11b A domain.
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页码:3619 / 3628
页数:10
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