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Human mesenchymal stem cells suppress induction of cytotoxic response to alloantigens

机译:人间充质干细胞抑制诱导血糖蛋白的细胞毒性反应

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Mesenchymal stem cells (MSC) fail to induce allogeneic responses in mixed lymphocyte reaction assays. Because MSC express HLA class I molecules, here we investaged whether they could be recognized as allogeneic targets by cytolytic T lymphocytes (CTL),. With this aim, CTL precursor (CTLp) frequencies were measured following stimulation of T cells with either allogeneic mononuclear cells (MNC) or MSC originated from the same human bone marrow donor. Lysis of MSC was measured at day 10 of culture in standard chromium release assays In addition, allogeneic PHA blast T cells or B-EBV lymphoblastoid cell lines (LCLs) generated from the same donor were used as positive controls of lysis. Our results showed that when allogeneic MNC were used to stimulate T cells, a high CTLp frequency was detected towards MSC targets. However, when MSC were used as stimulators, CTLp frequencies were markedly altered whatever the targets used, i.e.: MSC, PHA blast T cells or EBV-B LCLs. Moreover, when graded concentrations of MSC were added together with MNC upon stimulation of alloreactive T cells, we observed a dose-dependent decrease in CTLp frequencies towards MSC targets. This inhibition of MSC lysis was partially overcomed by adding exogenous rh-IL-2 fiom the beginning of cultures. In addition, this suppressive effect was totally reproduced when, instead of MSC, supernatant harvested from MSC cultures was added to allogeneic MNC, upon stimulation of alloreactive T cells. In conclusion, our results demonstrate that MSC which can be recognized as targets by pre-activated alloreactive CTLs, may be able to suppress differentiation of CTL precursors into CTL effectors through secretion of suppressive factors.
机译:间质干细胞(MSC)不能诱导在混合淋巴细胞反应测定同种异体反应。由于MSC表达HLA I类分子,在这里我们investaged他们是否可以被认为是由细胞毒性T淋巴细胞同种异体目标(CTL),.为了这个目的,CTL前体(CTLP)频率测量T细胞的刺激后与任一同种异体的单核细胞(MNC)或MSC源自同一人骨髓供体。 MSC的裂解在标准铬释放试验另外培养的第10天测量的,同种异体的PHA母T细胞或B-EBV淋巴母来自相同供体产生的细胞系(的LCL)用作裂解的阳性对照。我们的研究结果表明,当同种异体MNC用于刺激T细胞,被朝着目标MSC检测到高频率CTLP。但是,当MSC用作刺激器,CTLP频率均显着改变所使用的任何目标,即:MSC,PHA胚T细胞或EBV-B的LCL。此外,当MSC的梯度浓度连同MNC在同种异体反应性T细胞的刺激增加,我们观察到在朝向MSC目标CTLP频率的剂量依赖性降低。 MSC裂解的这种抑制部分被添加外源的rh-IL-2培养FIOM的开始克服了。此外,这种抑制效果完全再现时,而不是MSC,上清液从MSC培养物中收获加入到同种异体MNC,在同种异体反应性T细胞的刺激。总之,我们的结果表明,MSC可以被识别为通过预激活同种异体CTL的目标,或许能够CTL前体为CTL效应的抑制分化通过抑制因子的分泌。

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