A Subset of CD4 <sup>+</sup> Thymocytes Selected by MHC Class I Molecules

Albert Bendelac(National Institute of Allergy and Infectious Diseases), Nigel Killeen(Howard Hughes Medical Institute), Dan R. Littman(Howard Hughes Medical Institute), Ronald H. Schwartz(National Institute of Allergy and Infectious Diseases)
Science
March 25, 1994
Cited by 457

Abstract

To complete their maturation, most immature thymocytes depend on the simultaneous engagement of their antigen receptor [alpha beta T cell receptor (TCR)] and their CD4 or CD8 coreceptors with major histocompatibility complex class II or I ligands, respectively. However, a normal subset of mature alpha beta TCR+ thymocytes did not follow these rules. These thymocytes expressed NK1.1 and a restricted set of alpha beta TCRs that are intrinsically class I-reactive because their positive selection was class I-dependent but CD8-independent. These cells were CD4+ and CD4-8- but never CD8+, because the presence of CD8 caused negative selection. Thus, neither CD4 nor CD8 contributes signals that direct their maturation into the CD4+ and CD4-8- lineages.


Related Papers