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Interleukin-1 beta induces differential adhesiveness on human endothelial cell surfaces.

作者信息

Sung K L, Saldivar E, Phillips L

机构信息

Department of Orthopaedics, School of Medicine, University of California, San Diego, La Jolla 92093-0412.

出版信息

Biochem Biophys Res Commun. 1994 Jul 29;202(2):866-72. doi: 10.1006/bbrc.1994.2010.

DOI:10.1006/bbrc.1994.2010
PMID:7519425
Abstract

The adhesive strength between HL-60 and endothelial cells activated with IL-1 beta was investigated according to the region (area) on the endothelial cell surface where the HL-60 cell was attached (nuclear, junctional, or cytoplasmic). Using a micropipette single-cell manipulation system, we demonstrated that the increase of adhesive force was due to the activation of the endothelial cell with IL-1 beta and a function of the region of the endothelial cell. The increase in adhesion strength due to the increased expression of E-Selectin on the endothelial cell was studied by the addition of monoclonal antibodies against E-Selectin, ICAM-1, VCAM, and PECAM-1. Our findings suggest that the greatest adhesive strength was seen in the junctional region where the antibodies could not block the adhesion. However, the contribution of E-Selectin was significant in the nuclear region.

摘要

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