Programming for recognition and programming for response. Separate developmental subroutines in the murine thymus.

Thymus Pub Date : 1994-01-01
E V Rothenberg, R A Diamond, D Chen
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Abstract

Pre-T cells become programmed with the capacity to make functional responses to activating stimuli in a process that occurs prior to, and independently of, T-cell receptor gene rearrangement and T-cell receptor-dependent positive selection. In spite of this early programming, as differentiation proceeds further the cells enter a stage in which they appear to be unable to make any functional responses. This 'eclipse' phase begins when the cells undergo successful T-cell receptor beta-chain rearrangement and ends, with the return of their functional competence, only when they successfully traverse positive selection. These results suggest that pre-T cells are subject to two distinct subroutines of differentiation, which cannot operate at the same time: one which confers function and one which confers and selects recognition specificity. To provide a possible molecular basis for the relationship between these two processes, we consider specific alterations in response-associated transcription factors that may cause the changes in responsiveness observed during programming for recognition. The interplay of the two differentiation subroutines is proposed to be a consequence of the use of common transcription factors in different combinatorial contexts for functional responses, assembly of T-cell receptor complexes, and selection.

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识别编程和响应编程。小鼠胸腺的独立发育子程序。
在t细胞受体基因重排和t细胞受体依赖的阳性选择之前,预t细胞被编程为具有对激活刺激做出功能性反应的能力。尽管有这种早期编程,但随着分化的进一步进行,细胞进入了一个似乎无法做出任何功能性反应的阶段。当细胞成功地经历t细胞受体β链重排时,这个“日食”阶段开始,只有当它们成功地通过正选择时,它们的功能能力才会恢复。这些结果表明,前t细胞受到两种不同的分化子程序的影响,它们不能同时起作用:一种是赋予功能,另一种是赋予和选择识别特异性。为了为这两个过程之间的关系提供可能的分子基础,我们考虑了响应相关转录因子的特定改变,这些改变可能导致在编程识别过程中观察到的响应性变化。两种分化子程序的相互作用被认为是在不同的组合环境中使用共同转录因子的结果,用于功能反应,t细胞受体复合物的组装和选择。
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