The somatically generated portion of T cell receptor CDR3α contributes to the MHC allele specificity of the T cell receptor

Elife. 2017 Nov 17:6:e30918. doi: 10.7554/eLife.30918.

Abstract

Mature T cells bearing αβ T cell receptors react with foreign antigens bound to alleles of major histocompatibility complex proteins (MHC) that they were exposed to during their development in the thymus, a phenomenon known as positive selection. The structural basis for positive selection has long been debated. Here, using mice expressing one of two different T cell receptor β chains and various MHC alleles, we show that positive selection-induced MHC bias of T cell receptors is affected both by the germline encoded elements of the T cell receptor α and β chain and, surprisingly, dramatically affected by the non germ line encoded portions of CDR3 of the T cell receptor α chain. Thus, in addition to determining specificity for antigen, the non germline encoded elements of T cell receptors may help the proteins cope with the extremely polymorphic nature of major histocompatibility complex products within the species.

Keywords: CDR3 alpha; T cell receptor; immunology; major histocompatibility complex; mouse; selection; thymus.

Publication types

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

MeSH terms

  • Alleles*
  • Animals
  • Histocompatibility Antigens / genetics
  • Histocompatibility Antigens / metabolism*
  • Major Histocompatibility Complex*
  • Mice
  • Protein Binding
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Substrate Specificity

Substances

  • Histocompatibility Antigens
  • Receptors, Antigen, T-Cell