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

Proc Natl Acad Sci U S A. 2002 Jul 9;99(14):9410-4. doi: 10.1073/pnas.142586899. Epub 2002 Jul 1.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport, Active
  • Caco-2 Cells
  • DNA, Complementary / genetics
  • Enterocytes / metabolism
  • Enterocytes / virology
  • Epithelial Cells / metabolism
  • Epithelial Cells / virology
  • Galactosylceramides / genetics
  • Galactosylceramides / physiology
  • Gene Expression
  • HIV-1 / pathogenicity*
  • HIV-1 / physiology
  • Humans
  • Peyer's Patches / metabolism
  • Peyer's Patches / virology
  • Receptors, CCR5 / genetics
  • Receptors, CCR5 / physiology
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / physiology
  • Receptors, HIV / genetics
  • Receptors, HIV / physiology*
  • Transfection

Substances

  • DNA, Complementary
  • Galactosylceramides
  • Receptors, CCR5
  • Receptors, CXCR4
  • Receptors, HIV