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J Virol, May 1998, p. 4231-4236, Vol. 72, No. 5
Universitätsklinikum Rudolf Virchow,
Received 4 June 1997/Accepted 19 January 1998
Cell-free human immunodeficiency virus type 1 (HIV-1) can be taken
up and released by a monolayer of primary human gingival cells and
remain infectious for CD4+ cells. Virus-sized latex
particles covalently coated with purified native HIV-1 envelope
glycoprotein gp120 are also transported through the primary epithelial
cells. This process is significantly stimulated by increasing the
intracellular cyclic AMP (cAMP) concentration. Inhibition experiments
with mannan and
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Epithelial Uptake and Transport of Cell-Free Human
Immunodeficiency Virus Type 1 and gp120-Coated Microparticles
-methyl-mannopyranoside indicated that
mannosyl groups are involved in the interaction between gp120 and
gingival cells. An increase of cellular oligomannosyl receptors by
incubation with the mannosidase inhibitor deoxymannojirimycin augmented
transcellular transport of the gp120-coated particles. The results
suggest that infectious HIV can penetrate gingival epithelia by a
cAMP-dependent transport mechanism involving interaction of the
lectin-like domain of gp120 and mannosyl residues on glycoproteins on
the mucosal surface. Penetration of HIV could be inhibited by soluble
glycoconjugates present in oral mucins.
*
Corresponding author. Mailing address:
Universitätsklinikum Rudolf Virchow, Institut für Klinische
Chemie und Biochemie, Augustenburger Platz 1, D-13353 Berlin, Germany.
Phone: 49-30-450 69033. Fax: 49-30-450 69900. E-mail:
akage{at}ukrv.de.
J Virol, May 1998, p. 4231-4236, Vol. 72, No. 5
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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