T Cell Responses Modulated Through Interaction Between CD8αα and the Nonclassical MHC Class I Molecule, TL

Author:

Leishman Andrew J.1,Naidenko Olga V.1,Attinger Antoine1,Koning Frits12,Lena Christopher J.1,Xiong Yi3,Chang Hsiu-Ching3,Reinherz Ellis3,Kronenberg Mitchell1,Cheroutre Hilde1

Affiliation:

1. Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, CA 92121, USA.

2. Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, Netherlands.

3. Laboratory of Immunobiology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.

Abstract

The thymus leukemia antigen (TL) is a nonclassical class I molecule, expressed abundantly on intestinal epithelial cells. We show that, in contrast to other major histocompatibility complex (MHC) class I molecules that bind CD8αβ, TL preferentially binds the homotypic form of CD8α (CD8αα). Thus, TL tetramers react specifically to CD8αα-expressing cells, including most intestinal intraepithelial lymphocytes. Compared with CD8αβ, which recognizes the same MHC as the T cell receptor (TCR) and thus acts as a TCR coreceptor, high-affinity binding of CD8αα to TL modifies responses mediated by TCR recognition of antigen presented by distinct MHC molecules. These findings define a novel mechanism of lymphocyte regulation through CD8αα and MHC class I.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference29 articles.

1. Structure of a gene encoding a murine thymus leukemia antigen, and organization of Tla genes in the BALB/c mouse.

2. Expression of the thymus leukemia antigen in mouse intestinal epithelium.

3. Teitell M., et al., Crit. Rev. Immunol. 14, 1 (1994).

4. Soluble TL ( T18 d ) heavy chain was amplified by the polymerase chain reaction and cloned ahead of the BirA tag coding sequence into the Sal I/Bam HI sites of the mCD1/β 2 -microglobulin (β 2 m) pBacp10pH expression vector replacing the CD1d heavy chain. Baculovirus transfection recombinant protein production and biotinylation were done as previously described (26). TL tetramers were conjugated to streptavidin Tricolor (Caltag) or Neutravidin-PE (Molecular Probes). Tetramer staining was carried out as described (26) with 2.5 to 5 μg of tetramer protein. For blocking 1 μg of anti-TL antibody 18/20 or 0.5 μg of an CD8α-specific antibody (Caltag) was used; the 53-6.7 CD8α-specific antibody does not block TL tetramer staining.

5. Supplemental web material is available on Science Online at www.sciencemag.org/cgi/content/full/294/5548/1936/DC1.

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