Transepithelial transport of HIV-1 by M cells is receptor-mediated.
Détails
ID Serval
serval:BIB_7F4A301E9B37
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Transepithelial transport of HIV-1 by M cells is receptor-mediated.
Périodique
Proceedings of the National Academy of Sciences of the United States of America
ISSN
0027-8424
Statut éditorial
Publié
Date de publication
2002
Peer-reviewed
Oui
Volume
99
Numéro
14
Pages
9410-4
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't - Publication Status: ppublish
Résumé
Human colon carcinoma Caco-2 cell monolayers undergo conversion into cells that share morphological and functional features of M cells when allowed to interact with B lymphocytes. A lymphotropic (X4) HIV-1 strain crosses M cell monolayers and infects underlying CD4(+) target cells. Transport requires both lactosyl cerebroside and CXCR4 receptors, which are expressed on the apical surface of Caco-2 and M cells. Antibodies specific for each receptor block transport. In contrast, a monotropic (R5) HIV-1 strain is unable to cross M cell monolayers and infect underlying monocytes, despite efficient transport of latex beads. Caco-2 and M cells do not express CCR5, but transfection of these cells with CCR5 cDNA restores transport of R5 virus, which demonstrates that HIV-1 transport across M cells is receptor-mediated. The follicle-associated epithelium covering human gut lymphoid follicles expresses CCR5, but not CXCR4, and lactosyl cerebroside, suggesting that HIV-1 infection may occur through M cells and enterocytes at these sites.
Mots-clé
Biological Transport, Active, Caco-2 Cells, DNA, Complementary, Enterocytes, Epithelial Cells, Galactosylceramides, Gene Expression, HIV-1, Humans, Peyer's Patches, Receptors, CCR5, Receptors, CXCR4, Receptors, HIV, Transfection
Pubmed
Web of science
Open Access
Oui
Création de la notice
25/01/2008 17:02
Dernière modification de la notice
20/08/2019 15:40