| Literature DB >> 10435577 |
R E Berg1, M F Princiotta, S Irion, J A Moticka, K R Dahl, U D Staerz.
Abstract
Thymocytes are positively selected for alphabeta T cell antigen receptors (TCR) that recognize antigen in conjunction with self-major histocompatibility complex (MHC) molecules. MHC bound peptides participate in positive selection; however, their role has remained controversial. A TCR transgenic mouse was established using a TCR restricted to the MHC class Ib molecule, H2-M3. Having defined H2-M3 as the positively selecting MHC molecule, the severely limited number of H2-M3 binding peptides allowed us to characterize an NADH dehydrogenase subunit 1 (ND1)-derived peptide as the physiological ligand of positive selection. This peptide bears no apparent sequence homology to the cognate peptide, is expressed ubiquitously, and yet does not interfere with peripheral T cells. Our studies also suggest that positive selection becomes promiscuous at high epitope densities.Entities:
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Year: 1999 PMID: 10435577 DOI: 10.1016/s1074-7613(00)80079-5
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745