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PMID: 1375271 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Monocyte attachment to activated human vascular endothelium in vitro is mediated by leukocyte adhesion molecule-1 (L-selectin) under nonstatic conditions.

The Journal of experimental medicine ·Vol. 175 ·No. 6 ·1992-06-01 ·Pages 1789-92

Spertini O, Luscinskas FW, Gimbrone MA, Tedder TF

Abstract

The receptors that mediate monocyte adhesion to cytokine-stimulated endothelial monolayers were assessed using a nonstatic (rotating) cell-attachment assay. In this system, leukocyte adhesion molecule-1 (LAM-1) (L-selectin) mediated a major portion (87 +/- 15% at 37 degrees C) of monocyte attachment to activated endothelium. mAb blocking of endothelial leukocyte adhesion molecule-1 (41% inhibition), CD18 (36%), and vascular cell adhesion molecule-1 (25%) function had lesser effects on attachment. These results suggest that LAM-1 may serve an important role in monocyte attachment to endothelium at sites of inflammation.

MeSH Terms
Antibodies, Monoclonal Antigens, CD/physiology CD18 Antigens Cell Adhesion/drug effects Cell Adhesion Molecules/biosynthesis,immunology,physiology Cell Line Endothelium, Vascular/drug effects,physiology Humans L-Selectin Monocytes/drug effects,physiology Receptors, Leukocyte-Adhesion/physiology Tumor Necrosis Factor-alpha/drug effects Umbilical Veins Vascular Cell Adhesion Molecule-1
Chemicals
Antibodies, Monoclonal Antigens, CD CD18 Antigens Cell Adhesion Molecules Receptors, Leukocyte-Adhesion Tumor Necrosis Factor-alpha Vascular Cell Adhesion Molecule-1 L-Selectin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Spertini O
Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Luscinskas F W
Gimbrone M A
Tedder T F
References (14)
14 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1992-06-01
Pages
1789-92
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2119244
Subset
IM
Grants
NIAID NIH HHS · AI-26872 · United States
NCI NIH HHS · CA-34183 · United States
NCI NIH HHS · CA-36167 · United States
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