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CD4+8-和CD4-8+成熟胸腺细胞在最终发育过程中需要不同的选择后处理。

CD4+8- and CD4-8+ mature thymocytes require different post-selection processing for final development.

作者信息

Petrie H T, Strasser A, Harris A W, Hugo P, Shortman K

机构信息

Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.

出版信息

J Immunol. 1993 Aug 1;151(3):1273-9.

PMID:8101540
Abstract

Two primary types of TCR-alpha/beta+ T cells are found in the peripheral lymphoid system; CD4+8- T cells, with MHC-class II restricted TCR, and CD4-8+ T cells, which are MHC-class I restricted. Both lineages develop in the thymus from a series of common precursors. However, the precise stage at which they diverge, and the combination of factors that regulates such divergence, are not well defined. The up-regulation of CD3/TCR to high mature levels is thought to be an early event associated with positive selection for self-MHC recognition. Using purified cells from bcl-2 transgenic mice in order to overcome the limitations imposed by cell death on normal thymocytes, we find that a minor subset of CD4+8+ thymocytes expressing high levels of CD3/TCR gives rise to both CD4+8- and CD4-8+ mature cells upon intrathymic transplantation, but only to CD4-8+ in culture. Thus, in addition to demonstrating the dual lineage potential of this subset, these findings show that additional post-selection processing events are required for the production of mature thymocytes, and that CD4+8- and CD4-8+ subsets differ in the types of processing required.

摘要

在外周淋巴系统中可发现两种主要类型的TCR-α/β⁺ T细胞;具有MHC-II类限制性TCR的CD4⁺8⁻ T细胞,以及MHC-I类限制性的CD4⁻8⁺ T细胞。这两个谱系均在胸腺中由一系列共同前体发育而来。然而,它们发生分化的确切阶段以及调节这种分化的因素组合尚未明确界定。CD3/TCR上调至高成熟水平被认为是与自身MHC识别的阳性选择相关的早期事件。为了克服细胞死亡对正常胸腺细胞造成的限制,我们使用来自bcl-2转基因小鼠的纯化细胞,发现表达高水平CD3/TCR的CD4⁺8⁺胸腺细胞的一个小亚群在胸腺内移植后可产生CD4⁺8⁻和CD4⁻8⁺成熟细胞,但在培养中仅产生CD4⁻8⁺细胞。因此,除了证明该亚群具有双谱系潜能外,这些发现还表明,产生成熟胸腺细胞需要额外的选择后加工事件,并且CD4⁺8⁻和CD4⁻8⁺亚群在所需的加工类型上存在差异。

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