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Infection and Immunity, March 2000, p. 1080-1085, Vol. 68, No. 3
Program in Infectious Diseases, School of Public Health,
University of California, Berkeley, California
94720,1 and Departments of
Laboratory Medicine,2
Medicine,4 and Biomedical
Sciences5 and the Francis I. Proctor
Foundation,3 University of California, San
Francisco, California 94143
Received 12 July 1999/Returned for modification 30 August
1999/Accepted 15 November 1999
Using polystyrene microspheres coated with heparin or heparan
sulfate, it was shown that coated microspheres specifically bound
eukaryotic cells and were endocytosed by nonprofessional phagocytic
cells. Coated microspheres displayed properties of binding to
eukaryotic cells that were similar to those of chlamydiae, and the
microspheres were competitively inhibited by chlamydial organisms.
Endocytosis of heparin-coated beads resulted in the tyrosine
phosphorylation of a similar set of host proteins as did endocytosis of
chlamydiae; however, unlike viable chlamydial organisms, which prevent
phagolysosomal fusion, endocytosed beads were trafficked to a lysosomal
compartment. These findings suggest that heparin-coated beads and
Chlamydia trachomatis enter eukaryotic cells by similar pathways.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Eukaryotic Cell Uptake of Heparin-Coated
Microspheres: a Model of Host Cell Invasion by Chlamydia
trachomatis
*
Corresponding author. Mailing address: Program in
Infectious Diseases, 235 Earl Warren Hall, University of California,
Berkeley, CA 94720-7360. Phone: (510) 643-9900. Fax: (510) 643-5676. E-mail: rss{at}uclink4.berkeley.edu.
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