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PMID: 1714725 Published · ppublish English Journal Article

Expression and functional characterization of a soluble form of vascular cell adhesion molecule 1.

Biochemical and biophysical research communications ·Vol. 178 ·No. 3 ·1991-08-15 ·Pages 1498-504

Lobb R, Chi-Rosso G, Leone D, Rosa M, Newman B, Luhowskyj S, Osborn L, Schiffer S, Benjamin C, Dougas I

Abstract

Vascular cell adhesion molecule 1 (VCAM1) is a leukocyte adhesion molecule induced on human endothelium in vitro and in vivo by inflammatory stimuli. A truncated cDNA for VCAM1 was constructed, stably expressed in Chinese Hamster Ovary (CHO) cells, and the secreted recombinant soluble form of VCAM1 (rsVCAM1) purified to homogeneity by immunoaffinity chromatography. Immobilized rsVCAM1 is a functional adhesion protein, and selectively binds only VLA4-expressing cells, including human B and T lymphocytes, NK cells, and certain lymphoblastoid cell lines. T cell subset analyses indicate preferential binding of CD8+ memory cells. rsVCAM1 should prove valuable for the further study of the role of VCAM1 during inflammatory and immune responses in vivo.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Adhesion/drug effects Cell Adhesion Molecules/genetics,isolation & purification,pharmacology Cell Line Cell Membrane/physiology Codon Cytoplasm/physiology Genetic Vectors Humans Molecular Sequence Data Recombinant Proteins/isolation & purification,pharmacology T-Lymphocyte Subsets/immunology,physiology Transfection Vascular Cell Adhesion Molecule-1
Chemicals
Cell Adhesion Molecules Codon Recombinant Proteins Vascular Cell Adhesion Molecule-1
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Lobb R
Biogen Inc., Cambridge, MA 02142.
Chi-Rosso G
Leone D
Rosa M
Newman B
Luhowskyj S
Osborn L
Schiffer S
Benjamin C
Dougas I
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1991-08-15
Pages
1498-504
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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