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人骨髓间充质基质细胞通过 TNF-α 介导的 NF-κB 激活调节 T 细胞反应。

Human mesenchymal stromal cells modulate T-cell responses through TNF-α-mediated activation of NF-κB.

机构信息

Mesenchymal and Hematopoietic Stem Cell Laboratory, Foundation for Stem Cell Research, Fundación Inbiomed, San Sebastián, Spain.

出版信息

Eur J Immunol. 2014 Feb;44(2):480-8. doi: 10.1002/eji.201343668. Epub 2013 Dec 4.

Abstract

Although mesenchymal stromal cells (MSCs) possess the capacity to modulate immune responses, little is known about the mechanisms that underpin these processes. In this study, we show that immunosupression is mediated by activation of nuclear factor kappa B (NF-κB) in human MSCs. This pathway is activated by TNF-α that is generated following TCR stimulation of T cells. Inhibition of NF-κB through silencing of IκB kinase β or the TNF-α receptor abolishes the immunosuppressive capacity of MSCs. Our data also indicate that MSC-associated NF-κB activation primarily leads to inhibition of T-cell proliferation with little effect on expression of the activation markers CD69 and CD25. Thus, our data support the hypothesis that the TNF-α/NF-κB signalling pathway is required for the initial priming of immunosuppressive function in human MSCs. Interestingly, drugs that interfere with NF-κB activation significantly antagonise the immunoregulatory effect of MSCs, which could have important implications for immunosuppression regimens in the clinic.

摘要

虽然间充质基质细胞(MSCs)具有调节免疫反应的能力,但对于支持这些过程的机制知之甚少。在这项研究中,我们表明免疫抑制是通过人 MSCs 中核因子 kappa B(NF-κB)的激活介导的。该途径通过 T 细胞 TCR 刺激后产生的肿瘤坏死因子-α(TNF-α)激活。通过沉默 IκB 激酶 β 或 TNF-α 受体抑制 NF-κB,可消除 MSCs 的免疫抑制能力。我们的数据还表明,MSC 相关的 NF-κB 激活主要导致 T 细胞增殖抑制,而对激活标志物 CD69 和 CD25 的表达影响很小。因此,我们的数据支持这样一种假设,即 TNF-α/NF-κB 信号通路是人类 MSCs 中初始免疫抑制功能的初始启动所必需的。有趣的是,干扰 NF-κB 激活的药物可显著拮抗 MSCs 的免疫调节作用,这对于临床免疫抑制方案可能具有重要意义。

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