Bhandoola A, Cibotti R, Punt J A, Granger L, Adams A J, Sharrow S O, Singer A
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Immunity. 1999 Mar;10(3):301-11. doi: 10.1016/s1074-7613(00)80030-8.
During positive selection, immature thymocytes commit to either the CD4+ or CD8+ T cell lineage ("commitment") and convert from short-lived thymocytes into long-lived T cells ("rescue"). By formal precursor-progeny analysis, we now identify what is likely to be the initial positive selection step signaled by alpha beta TCR, which we have termed "induction". During induction, RAG mRNA expression is downregulated, but lineage commitment does not occur. Rather, lineage commitment (which depends upon the MHC class specificity of the alpha beta TCR) only occurs after downregulation of RAG expression and the consequent fixation of alpha beta TCR specificity. We propose that positive selection can be viewed as a sequence of increasingly selective developmental steps (induction-->commitment-->rescue) that are signaled by alpha beta TCR engagements of intrathymic ligands.
在阳性选择过程中,未成熟胸腺细胞分化为CD4⁺或CD8⁺T细胞谱系(“分化”),并从短命的胸腺细胞转变为长寿的T细胞(“拯救”)。通过正式的前体-子代分析,我们现在确定了可能是由αβTCR发出信号的初始阳性选择步骤,我们将其称为“诱导”。在诱导过程中,RAG mRNA表达下调,但谱系分化并未发生。相反,谱系分化(其取决于αβTCR的MHC类别特异性)仅在RAG表达下调以及随后αβTCR特异性固定后才会发生。我们提出,阳性选择可被视为一系列由胸腺内配体的αβTCR结合所发出信号的、选择性越来越高的发育步骤(诱导→分化→拯救)。