Characterization of a proteasome and TAP-independent presentation of intracellular epitopes by HLA-B27 molecules. - RIIP - Réseau International des Instituts Pasteur Accéder directement au contenu
Article Dans Une Revue Journal of Biological Chemistry Année : 2012

Characterization of a proteasome and TAP-independent presentation of intracellular epitopes by HLA-B27 molecules.

Résumé

Nascent HLA-class I molecules are stabilized by proteasome-derived peptides in the ER and the new complexes proceed to the cell surface through the post-ER vesicles. It has been shown, however, that less stable complexes can exchange peptides in the Trans Golgi Network (TGN). HLA-B27 are the most studied HLA-class I molecules due to their association with Ankylosing Spondylitis (AS). Chimeric proteins driven by TAT of HIV have been exploited by us to deliver viral epitopes, whose cross-presentation by the HLA-B27 molecules was proteasome and TAP-independent and not restricted to Antigen-Presenting Cells (APC). Here, using these chimeric proteins as epitope suppliers, we compared with each other and with the HLA-A2 molecules, the two HLA-B*2705 and B*2709 alleles differing at residue 116 (D116H) and differentially associated with AS. We found that the antigen presentation by the two HLA-B27 molecules was proteasome-, TAP-, and APC-independent whereas the presentation by the HLA-A2 molecules required proteasome, TAP and professional APC. Assuming that such difference could be due to the unpaired, highly reactive Cys-67 distinguishing the HLA-B27 molecules, C67S mutants in HLA-B*2705 and B*2709 and V67C mutant in HLA-A*0201 were also analyzed. The results showed that this mutation did not influence the HLA-A2-restricted antigen presentation while it drastically affected the HLA-B27-restricted presentation with, however, remarkable differences between B*2705 and B*2709. The data, together with the occurrence on the cell surface of unfolded molecules in the case of C67S-B*2705 mutant but not in that of C67S-B*2709 mutant, indicates that Cys-67 has a more critical role in stabilizing the B*2705 rather than the B*2709 complexes.

Domaines

Immunologie

Dates et versions

pasteur-00965699 , version 1 (25-03-2014)

Identifiants

Citer

Adriana Magnacca, Irene Persiconi, Elisa Nurzia, Silvana Caristi, Francesca Meloni, et al.. Characterization of a proteasome and TAP-independent presentation of intracellular epitopes by HLA-B27 molecules.. Journal of Biological Chemistry, 2012, 287 (36), pp.30358-67. ⟨10.1074/jbc.M112.384339⟩. ⟨pasteur-00965699⟩

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