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  4. Transepithelial transport of HIV-1 by M cells is receptor-mediated
 
research article

Transepithelial transport of HIV-1 by M cells is receptor-mediated

Fotopoulos, Grigorios
•
Harari, Alexandre
•
Michetti, Pierre
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2002
Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS)

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.

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Type
research article
DOI
10.1073/pnas.142586899
Author(s)
Fotopoulos, Grigorios
Harari, Alexandre
Michetti, Pierre
Trono, Didier  
Pantaleo, Giuseppe
Kraehenbuhl, Jean-Pierre
Date Issued

2002

Publisher

National Academy of Sciences

Published in
Proceedings Of The National Academy Of Sciences Of The United States Of America (PNAS)
Volume

99

Issue

14

Start page

9410

End page

4

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LVG  
Available on Infoscience
September 5, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/215881
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