Antigen-presenting function of mouse CD1: one molecule with two different kinds of antigenic ligands

L Brossay1, N Burdin, S Tangri

  • 1Division of Developmental Immunology, La Jolla, Institute of Allergy and Immunology, San Diego, California, USA. Brossay@liai.org

Immunological Reviews
|August 13, 1998
PubMed

Insights

Mouse CD1 (mCD1) molecules present peptides and lipids to T cells. Autoreactive T cells distinguish cell types expressing mCD1, suggesting unique ligand roles in immune responses.

Area of Science:

  • Immunology
  • Molecular Biology
  • Structural Biology

Background:

  • Mouse CD1 (mCD1) is an antigen-presenting molecule on bone marrow-derived cells.
  • mCD1 presents peptides to CD8+ T cells and is recognized by autoreactive NK1.1+ T cells.
  • NK T cells' cytokine production suggests immunoregulatory roles.

Purpose of the Study:

  • To investigate the role of mCD1-bound autologous ligands in T-cell stimulation.
  • To understand how mCD1 accommodates diverse ligands, including peptides and lipids.

Main Methods:

  • Analysis of mCD1-autoreactive T cell responses to different cell types.
  • Assessment of T cell recognition of alpha-galactosylceramide presented by mCD1.
  • Examination of the mCD1 crystal structure and its antigen-binding site.

Main Results:

  • mCD1-autoreactive T cells differentiate between cell types expressing similar mCD1 levels.
  • Some mCD1-restricted T cells recognize alpha-galactosylceramide, while others do not.
  • The mCD1 antigen-binding site is deep and narrow, favoring lipid antigens over peptides.

Conclusions:

  • Autologous ligands bound to mCD1 are critical for T-cell stimulation.
  • mCD1's structure suggests a preference for lipid antigens, posing questions about accommodating peptide antigens.

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