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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对同种异体抗原的细胞毒性反应的诱导

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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 from 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:在混合淋巴细胞反应测定中,间充质干细胞(MSC)无法诱导同种异体反应。由于MSC表达HLA I类分子,因此我们在这里研究了它们是否可以被溶细胞性T淋巴细胞(CTL)识别为同种异体靶标。为此目的,在用同种人骨髓供体来源的同种异体单核细胞(MNC)或MSC刺激T细胞后,测量CTL前体(CTLp)的频率。在培养的第10天,以标准铬释放测定法测量MSC的裂解。此外,将从同一个供体产生的同种异体PHA blast T细胞或B-EBV淋巴母细胞样细胞系(LCL)用作裂解的阳性对照。我们的结果表明,当使用异源MNC刺激T细胞时,针对MSC目标的CTLp频率较高。但是,当使用MSC作为刺激物时,无论使用何种靶标,即MSC,PHA blast T细胞或EBV-B LCL,CTLp频率都会发生明显变化。此外,当刺激同种反应性T细胞后,将分级浓度的MSC与MNC一起添加时,我们观察到了朝向MSC靶标的CTLp频率呈剂量依赖性下降。通过从培养开始添加外源rh-IL-2,部分克服了对MSC裂解的抑制。另外,当刺激同种异体性T细胞时,当从MSC培养物中收获的上清液代替MSC而代替异种MSC时,完全抑制了这种抑制作用。总之,我们的结果表明,可以被预激活的同种反应性CTL识别为靶标的MSC可能能够通过分泌抑制因子来抑制CTL前体分化为CTL效应子。

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