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. 1990 Apr 1;171(4):1369-74.
doi: 10.1084/jem.171.4.1369.

Inducible cell adhesion molecule 110 (INCAM-110) is an endothelial receptor for lymphocytes. A CD11/CD18-independent adhesion mechanism

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Inducible cell adhesion molecule 110 (INCAM-110) is an endothelial receptor for lymphocytes. A CD11/CD18-independent adhesion mechanism

G E Rice et al. J Exp Med. .

Abstract

Inducible cell adhesion molecule 110 (INCAM-110) is a 110-kD glycoprotein expressed on cytokine-activated human vascular endothelial cells. mAb blocking studies indicate that INCAM-110 and intercellular adhesion molecule 1 (ICAM-1) independently support the adhesion of lymphocytes to activated human umbilical vein endothelial cell monolayers. Anti-CD11a/CD18 antibodies with anti-INCAM-110 mAb E1/6 produce greater inhibition of lymphocyte adhesion than either reagent alone, suggesting that INCAM-110 and LFA-1 are not an obligate receptor-ligand pair. Blood monocytes, but not polymorphonuclear leukocytes, also appear to bind endothelial INCAM-110. Endothelial expression of INCAM-110 is upregulated at sites of inflammation, suggesting a role in the recruitment of mononuclear leukocytes.

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References

    1. Proc Natl Acad Sci U S A. 1987 Dec;84(24):9238-42 - PubMed
    1. J Cell Biol. 1988 Jul;107(1):321-31 - PubMed
    1. J Immunol. 1986 Jul 1;137(1):245-54 - PubMed
    1. J Immunol. 1986 Sep 15;137(6):1893-6 - PubMed
    1. J Cell Physiol. 1988 Nov;137(2):305-9 - PubMed

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