International Immunology, Vol. 13, No. 1, 63-73,
January 2001
© 2001 Japanese Society for Immunology
Genetic control of peripheral TCRAV usage by representation in the preselection repertoire and MHC allele-specific overselection
Institute for Virology and Immunobiology, University of Würzburg, Versbacher Strasse 7, 97078 Würzburg, Germany
1 Immunogenetics Laboratory, Babraham Institute, Cambridge CB2 4AT, UK
2 Present Address: UPCM, Unite CNRS 1590, CHU Purpan, 31300 Toulouse, France
Correspondence to: T. Hünig
TCRAV segments contribute significantly to MHC restriction as illustrated by their general preference for either the CD4 or CD8 T cell subset and additional, MHC allele-specific overselection during T cell differentiation. The 10-fold over-representation of the TCRAV8S2 (VA8S2) segment in CD8 over CD4 T cells by the RT1f haplotype of LEW.1F rats provides the most striking example of MHC allele-specific overselection of a VA segment reported so far. Also in alloreactivity, VA8S2+ CD8 cells from RT1f– rats are preferentially expanded by RT1f+ stimulators. We have identified the class I molecule, Af, mediating VA8S2 overselection and report that it differs only in four amino acids at the MHC–TCR interface from the class I molecule Aa, which is neutral with regard to selection of VA8S2. We also provide an extensive survey of the TCRAV8 family and show that among 14 functional VA8 segments in LEW rats, the dramatic Af-dependent overselection is unique for VA8S2. Surprisingly, VA8S2 expression in CD8 T cells of RT1f+ rats derived from a Sprague-Dawley stock was only 3% as compared to the 12% observed in LEW.1F. The VA8S2 segment of Sprague-Dawley (VA8S2SD) differs from VA8S2 of the LEW background (VA8S2l) in only two amino acids, one of which is located in CDR2 and could thus participate in allele-specific recognition of Af. However, analysis of the pre- and postselection thymic repertoires of Sprague-Dawley and LEW.1F rats and of the repertoire of CD8 cells from both strains expanded in the alloreactive response to RT1f revealed that the difference in VA8S2 representation between the two backgrounds is explained by differential availability in the preselection repertoires and not by a difference in overselection. Sequence comparisons of Af and Aa and of both VA8S2 segments suggest a predominant role of CDR1 in hyper-reactivity to Af. Thus, the VA composition of the mature TCR repertoire is influenced by Tcra locus polymorphisms at two levels: the regulation of VA usage in the preselection repertoire and the composition of structural elements which contribute to specific VA–MHC interactions during thymic selection.
Keywords: alloreactivity, MHC recognition, rat, RT1, T cell repertoire, thymic selection
The first two authors contributed equally to this work
Transmitting editor: H. R. MacDonald
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