C-type lectin Mermaid inhibits dendritic cell mediated HIV-1 transmission to CD4+ T cells

Virology. 2008 Sep 1;378(2):323-8. doi: 10.1016/j.virol.2008.05.025. Epub 2008 Jul 1.

Abstract

Dendritic cells (DCs) are important in HIV-1 transmission; DCs capture invading HIV-1 through the interaction of the gp120 oligosaccharides with the C-type lectin DC-SIGN and migrate to the lymphoid tissues where HIV-1 is transmitted to T cells. Thus, the HIV-1 envelope glycoprotein gp120 is an attractive target to prevent interactions with DCs and subsequent viral transmission. Here, we have investigated whether the structural homologue of DC-SIGN, the nematode C-type lectin Mermaid can be used to prevent HIV-1 transmission by DCs. Our data demonstrate that Mermaid interacts with high mannose structures present on HIV-1 gp120 and thereby inhibits HIV-1 binding to DC-SIGN on DCs. Moreover, Mermaid inhibits DC-SIGN-mediated HIV-1 transmission from DC to T cells. We have identified Mermaid as a non-cytotoxic agent that shares the glycan specificity with DC-SIGN and inhibits DC-SIGN-gp120 interaction. The results are important for the anti-HIV-1 microbicide development directed at preventing DC-HIV-1 interactions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-HIV Agents / pharmacology*
  • CD4-Positive T-Lymphocytes / virology*
  • Cell Adhesion Molecules / metabolism
  • Cell Line
  • Cells, Cultured
  • Dendritic Cells / virology*
  • HIV Envelope Protein gp120 / metabolism
  • HIV-1 / drug effects*
  • Helminth Proteins / pharmacology*
  • Helminth Proteins / toxicity
  • Humans
  • Lectins, C-Type / metabolism*
  • Nematoda
  • Protein Binding
  • Receptors, Cell Surface / metabolism
  • Virus Attachment

Substances

  • Anti-HIV Agents
  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • HIV Envelope Protein gp120
  • Helminth Proteins
  • Lectins, C-Type
  • Receptors, Cell Surface