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小鼠TCRαβ⁺CD4⁻CD8⁻胸腺细胞的胸腺内选择

Intrathymic selection of murine TCR alpha beta+CD4-CD8- thymocytes.

作者信息

Egerton M, Scollay R

机构信息

Walter and Eliza Hall Institute of Medical Research, Royal Parade, Parkville, Australia.

出版信息

Int Immunol. 1990;2(2):157-63. doi: 10.1093/intimm/2.2.157.

DOI:10.1093/intimm/2.2.157
PMID:2128465
Abstract

The CD4-CD8- thymocyte population contains the precursors of all other thymocytes. However, it also contains a significant proportion of cells which express surface TCR alpha beta, and have little or no precursor activity. Like peripheral T cells, but unlike most other thymocytes, these TCR alpha beta+CD4-CD8- thymocytes do not express heat stable antigen. Both the origin and developmental status of these cells are unclear, and are the subject of this report. We have measured the proportion of V beta 8.1+ cells amongst TCR+HSA-CD4-CD8- thymocytes in MIs-1a versus MIs-1b mice, in order to determine whether they have undergone negative selection. The proportions were similar in both strains, in contrast to mature T cells, indicating that neither they nor their precursors had undergone clonal deletion. We also measured the accumulation of these cells over the early life of the animal and found that it was extremely slow. Our data also show that although TCR-V beta 8.1+ cells are reactive to MIs-1a in association with MHC class II, most mature TCR-V beta 8.1+ cells in MIs-1b mice are CD8+, suggesting an additional reactivity with MHC class I. We raise the possibility that TCR-V beta 8.1+CD4-CD8- thymocytes are derived from TCR-V beta 8.1+CD4+CD8+ thymocytes, and that the reactivity of TCR-V beta 8.1 with both MHC classes I and II has resulted in the down-regulation of both CD4 and CD8.

摘要

CD4-CD8-胸腺细胞群体包含所有其他胸腺细胞的前体。然而,它也包含相当比例的细胞,这些细胞表达表面TCRαβ,且几乎没有或完全没有前体活性。与外周T细胞一样,但与大多数其他胸腺细胞不同,这些TCRαβ+CD4-CD8-胸腺细胞不表达热稳定抗原。这些细胞的起源和发育状态尚不清楚,是本报告的主题。我们测量了MIs-1a与MIs-1b小鼠中TCR+HSA-CD4-CD8-胸腺细胞中Vβ8.1+细胞的比例,以确定它们是否经历了阴性选择。与成熟T细胞相反,两种品系中的比例相似,这表明它们及其前体均未经历克隆缺失。我们还测量了这些细胞在动物早期生命中的积累情况,发现其极其缓慢。我们的数据还表明,尽管TCR-Vβ8.1+细胞与MIs-1a结合MHC II类具有反应性,但MIs-1b小鼠中大多数成熟的TCR-Vβ8.1+细胞是CD8+,这表明它们与MHC I类还有额外的反应性。我们提出了TCR-Vβ8.1+CD4-CD8-胸腺细胞源自TCR-Vβ8.1+CD4+CD8+胸腺细胞的可能性,并且TCR-Vβ8.1与MHC I类和II类的反应性导致了CD4和CD8的下调。

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Intrathymic selection of murine TCR alpha beta+CD4-CD8- thymocytes.小鼠TCRαβ⁺CD4⁻CD8⁻胸腺细胞的胸腺内选择
Int Immunol. 1990;2(2):157-63. doi: 10.1093/intimm/2.2.157.
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An NK1.1+ CD4+8- single-positive thymocyte subpopulation that expresses a highly skewed T-cell antigen receptor V beta family.一个表达高度偏向性T细胞抗原受体Vβ家族的NK1.1⁺ CD4⁺8⁻单阳性胸腺细胞亚群。
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Phenotype, ontogeny, and repertoire of CD4-CD8- T cell receptor alpha beta + thymocytes. Variable influence of self-antigens on T cell receptor V beta usage.CD4-CD8-T细胞受体αβ+胸腺细胞的表型、个体发生及谱系。自身抗原对T细胞受体Vβ使用的可变影响。
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Timing of deletion of autoreactive V beta 6+ cells and down-modulation of either CD4 or CD8 on phenotypically distinct CD4+8+ subsets of thymocytes expressing intermediate or high levels of T cell receptor.在表达中高水平T细胞受体的胸腺细胞的表型不同的CD4⁺8⁺亚群上,自身反应性Vβ6⁺细胞的缺失时间以及CD4或CD8的下调情况。
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Fc gamma RII/III and CD2 expression mark distinct subpopulations of immature CD4-CD8- murine thymocytes: in vivo developmental kinetics and T cell receptor beta chain rearrangement status.FcγRII/III和CD2表达标记未成熟CD4-CD8-小鼠胸腺细胞的不同亚群:体内发育动力学和T细胞受体β链重排状态。
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Kidney Int. 2022 Jul;102(1):25-37. doi: 10.1016/j.kint.2022.02.035. Epub 2022 Apr 9.
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Double negative regulatory T cells in transplantation and autoimmunity: recent progress and future directions.
移植和自身免疫中的双重负调控 T 细胞:最新进展和未来方向。
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Quick recovery in the generation of self-reactive CD4low natural killer (NK) T cells by an alternative intrathymic pathway when restored from acute thymic atrophy.当从急性胸腺萎缩恢复时,通过另一种胸腺内途径快速恢复自身反应性CD4低自然杀伤(NK)T细胞的产生。
Clin Exp Immunol. 1999 Sep;117(3):587-95. doi: 10.1046/j.1365-2249.1999.00988.x.
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Autoreactive CD4- CD8- alpha beta T cells to vaccinate adjuvant arthritis.针对佐剂性关节炎的自身反应性CD4 - CD8 - αβ T细胞。
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A monoclonal antibody, DL10, which recognizes a sugar moiety of MHC class I antigens expressed on NK cells, NK+ T cells, and granulocytes in humans.一种单克隆抗体DL10,它能识别在人类自然杀伤细胞、自然杀伤T细胞和粒细胞上表达的MHC I类抗原的糖部分。
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Self-reactive forbidden clones are confined to pathways of intermediate T-cell receptor cell differentiation even under immunosuppressive conditions.即使在免疫抑制条件下,自身反应性禁忌克隆也局限于中间T细胞受体细胞分化途径。
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