首页> 外文期刊>The journal of immunology >Human Vascular Endothelial Cells Stimulate a Lower Frequency of Alloreactive CD8+ Pre-CTL and Induce Less Clonal Expansion than Matching B Lymphoblastoid Cells: Development of a Novel Limiting Dilution Analysis Method Based on CFSE Labeling of Lymphocytes
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Human Vascular Endothelial Cells Stimulate a Lower Frequency of Alloreactive CD8+ Pre-CTL and Induce Less Clonal Expansion than Matching B Lymphoblastoid Cells: Development of a Novel Limiting Dilution Analysis Method Based on CFSE Labeling of Lymphocytes

机译:与匹配的B淋巴母细胞相比,人血管内皮细胞刺激同种反应性CD8 + Pre-CTL的频率更低,并导致更少的克隆扩增:基于CFSE标记的淋巴细胞的新型极限稀释分析方法的开发

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We have previously shown that human endothelial cells (EC) are less efficient than professional APC, e.g., B lymphoblastoid cells (BLC), at stimulating allogeneic CD8+ T cells to develop into CTL. In this study we describe FACS-based limiting dilution analyses using the dilution of the intracellular dye CFSE as an indicator of CD8+ T cell alloactivation and expansion with significantly increased sensitivity compared with conventional, cytotoxicity-based assays. In addition, this assay permits the relative size of clonal CTL populations that are generated in individual CD8+ T cell cultures to be determined (clonal burst size). We have applied this method to quantitatively compare the generation of CTL at the clonal level following stimulation of allogeneic CD8+ T cells by either BLC or HUVEC derived from the same donor. CD8+ T cells expanded by allostimulation were identified as CD8+, CFSElow cells and were categorized as CTL by the expression of intracellular perforin and IFN-γ. Precursor frequencies for EC-stimulated CTL were 5- to 40-fold (mean, 7.5-fold) lower compared with BLC-stimulated CTL ( p 0.01). Concomitantly, the average clonal burst sizes in EC-stimulated CTL cultures were significantly smaller than those in conventional CTL cultures, primarily due to the occurrence of some very large clone sizes exclusively with BLC stimulation. Although EC-stimulated CTL were generated only from the memory subset of CD8+ T cells, BLC-stimulated very large burst sizes of CTL were observed from both naive and memory CD8+ T cell precursors. These data establish that both a lower frequency of reactive precursors and more limited clonal expansion, but not regulatory T cells, contribute to the reduced capacity of EC to promote alloreactive CTL differentiation compared with that of professional APC.
机译:先前我们已经表明,人内皮细胞(EC)在刺激同种异体CD8 + T细胞发展为CTL方面不如专业APC(例如B淋巴母细胞(BLC))有效。在这项研究中,我们描述了基于FACS的有限稀释分析,其中使用细胞内染料CFSE的稀释液作为CD8 + T细胞同种激活和扩增的指标,与传统的基于细胞毒性的分析方法相比,其灵敏度大大提高。另外,该测定允许确定在单个CD8 + T细胞培养物中产生的克隆CTL群体的相对大小(克隆爆发大小)。我们已应用此方法定量比较了来自同一供体的BLC或HUVEC刺激同种CD8 + T细胞后在克隆水平上CTL的生成。通过同种异体刺激扩增的CD8 + T细胞被鉴定为CD8 +,CFSElow细胞,并通过细胞内穿孔素和IFN-γ的表达归类为CTL。 EC刺激的CTL的前体频率比BLC刺激的CTL低5至40倍(平均7.5倍)(p <0.01)。相应地,EC刺激的CTL培养物中的平均克隆爆发大小显着小于常规CTL培养中的克隆爆发大小,这主要是由于仅BLC刺激而出现了一些非常大的克隆大小。尽管EC刺激的CTL仅从CD8 + T细胞的记忆子集生成,但从幼稚和记忆CD8 + T细胞前体中都观察到BLC刺激的CTL爆发非常大。这些数据表明,与专业APC相比,较低的反应性前体频率和更有限的克隆扩增(而不是调节性T细胞)均导致EC促进同种反应性CTL分化的能力降低。

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