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The T-cell receptor is not hardwired to engage MHC ligands.
Holland, Stephen J; Bartok, Istvan; Attaf, Meriem; Genolet, Raphael; Luescher, Immanuel F; Kotsiou, Eleni; Richard, Ashkenaz; Wang, Edward; White, Matthew; Coe, David J; Chai, Jian-Guo; Ferreira, Cristina; Dyson, Julian.
Afiliación
  • Holland SJ; Molecular Immunology Section, Division of Immunology and Inflammation, Imperial College London, Hammersmith Hospital, London W12 0NN, United Kingdom. holland@ie-freiburg.mpg.de
Proc Natl Acad Sci U S A ; 109(45): E3111-8, 2012 Nov 06.
Article en En | MEDLINE | ID: mdl-23077253
The bias of αß T cells for MHC ligands has been proposed to be intrinsic to the T-cell receptor (TCR). Equally, the CD4 and CD8 coreceptors contribute to ligand restriction by colocalizing Lck with the TCR when MHC ligands are engaged. To determine the importance of intrinsic ligand bias, the germ-line TCR complementarity determining regions were extensively diversified in vivo. We show that engagement with MHC ligands during thymocyte selection and peripheral T-cell activation imposes remarkably little constraint over TCR structure. Such versatility is more consistent with an opportunist, rather than a predetermined, mode of interface formation. This hypothesis was experimentally confirmed by expressing a hybrid TCR containing TCR-γ chain germ-line complementarity determining regions, which engaged efficiently with MHC ligands.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Antígenos de Linfocitos T alfa-beta / Complejo Mayor de Histocompatibilidad Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2012 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Antígenos de Linfocitos T alfa-beta / Complejo Mayor de Histocompatibilidad Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2012 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos