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Evaluation of TCR Vβ subfamily T cell expansion in NOD/SCID mice transplanted with human cord blood hematopoietic stem cells

机译:移植人脐血造血干细胞的NOD / SCID小鼠中TCRVβ亚家族T细胞扩增的评估

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摘要

Examination of the T cell receptor (TCR) gene repertoire is important in the analysis of the immune status of models, because clonal expansion of T cells permits the identification of specific antigen responses of T cells. Little is known about T-cell immunity in the humanized NOD/SCID mouse model. TCR Vβ repertoire usage and clonality were analyzed to investigate the distribution and clonal expansion of TCR Vβ subfamily T cells in NOD/SCID mice transplanted with human cord blood (CB) hematopoietic stem cells. The NOD/SCID mice were sublethally irradiated (60Co, 300cGy) to eliminate residual innate immunity in the host. The experimental mice were transplanted intravenously with CB CD34+ cells sorted by MACS. After 6 weeks, RNA was obtained from peripheral blood, bone marrow and thymus of the study animals. The gene expression and clonality of the TCR Vβ repertoire were determined by RT-PCR and GeneScan techniques. A restricted range of TCR Vβ usage was exhibited in the bone marrow of mice, which included TCR Vβ 1, 2, 9, 13 and 19. Further, oligoclonal expression of some TCR Vβ subfamilies (Vβ9, 13, 19) was identified by GeneScan technique. To investigate the reason for oligoclonal expansion of the TCR Vβ subfamily T cells from CB in mouse models, the T-cell culture with tissue-antigen of NOD/SCID mouse was performed in vitro. The cells from peripheral blood mononuclear cells and bone marrow, spleen, thymus in NOD/SCID mice were frozen and thawed, and used as tissue-antigen. CB mononuclear cells were separately cultured with the component from those murine cells for 15-20 days. Oligoclonal expression or oligoclonal trend of some TCR Vβ subfamilies (Vβ10, 11 and Vβ2, 15, 16, 19) was detected in T cells after stimulation with tissue-antigen of NOD/SCID mouse. Interestingly, a similar clonal expansion of the TCR Vβ11 subfamily was found in T cells cultured with peripheral blood, bone marrow and spleen respectively. The TCR Vβ subfamily T cells could be reconstituted in humanized NOD/SCID mouse transplanted with CD34+ cells from CB. The restricted expression and clonal expansion of some CB T cell clones may be induced by tissue-antigens of NOD/SCID mice.
机译:在分析模型的免疫状态时,T细胞受体(TCR)基因库的检查很重要,因为T细胞的克隆扩增可以鉴定T细胞的特异性抗原反应。关于人源化NOD / SCID小鼠模型中T细胞免疫的了解甚少。分析了TCRVβ库的用法和克隆性,以研究TCRVβ亚家族T细胞在人脐血(CB)造血干细胞移植后的NOD / SCID小鼠中的分布和克隆扩增。皮下注射NOD / SCID小鼠( 60 Co,300cGy),以消除宿主体内残留的先天免疫力。用MACS分选出的CB CD34 + 细胞进行静脉移植。 6周后,从研究动物的外周血,骨髓和胸腺中获得RNA。通过RT-PCR和GeneScan技术确定TCRVβ库的基因表达和克隆性。在小鼠的骨髓中显示出有限的TCRVβ使用范围,其中包括TCRVβ1、2、9、13和19。此外,GeneScan还鉴定了某些TCRVβ亚家族(Vβ9、13、19)的寡克隆表达。技术。为了研究小鼠模型中来自CB的TCRVβ亚家族T细胞寡克隆扩增的原因,在体外进行了具有NOD / SCID小鼠组织抗原的T细胞培养。将来自NOD / SCID小鼠的外周血单核细胞和骨髓,脾,胸腺的细胞冷冻并融化,并用作组织抗原。将CB单核细胞与来自那些鼠细胞的组分分别培养15-20天。用NOD / SCID小鼠的组织抗原刺激后,在T细胞中检测到某些TCRVβ亚家族的寡克隆表达或寡克隆趋势(Vβ10、11和Vβ2、15、16、19)。有趣的是,在分别用外周血,骨髓和脾培养的T细胞中发现了TCRVβ11亚家族的类似克隆扩增。 TCRVβ亚家族T细胞可以在人源化NOD / SCID小鼠体内重建,该小鼠移植了来自CB的CD34 + 细胞。 NOB / SCID小鼠的组织抗原可能诱导某些CB T细胞克隆的表达受限和克隆扩增。

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  • 来源
    《Hematology》 |2007年第4期|325-330|共6页
  • 作者单位

    Department of Microbiology and Immunology, Medical College of Jinan University, Guangzhou 510632, P. R. China;

    Institute of Hematology, Medical College of Jinan University, Guangzhou 510632, P. R. China;

    Institute of Hematology, Medical College of Jinan University, Guangzhou 510632, P. R. China;

    Department of Microbiology and Immunology, Medical College of Jinan University, Guangzhou 510632, P. R. China;

    Department of Microbiology and Immunology, Medical College of Jinan University, Guangzhou 510632, P. R. China;

    Institute of Hematology, Medical College of Jinan University, Guangzhou 510632, P. R. China;

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  • 入库时间 2022-08-17 23:34:42

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