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首页> 外文期刊>Mediators of inflammation >Interaction with Mesenchymal Stem Cells Provokes Natural Killer Cells for Enhanced IL-12/IL-18-Induced Interferon-Gamma Secretion
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Interaction with Mesenchymal Stem Cells Provokes Natural Killer Cells for Enhanced IL-12/IL-18-Induced Interferon-Gamma Secretion

机译:与间充质干细胞的相互作用激发天然杀伤细胞增强IL-12 / IL-18诱导的干扰素γ分泌。

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摘要

Tissue injury induces an inflammatory response accompanied by the recruitment of immune cells and of mesenchymal stem cells (MSC) that contribute to tissue regeneration. After stimulation with interleukin- (IL-) 12 and IL-18 natural killer (NK) cells secrete the proinflammatory cytokine interferon- (IFN-)γ. IFN-γplays a crucial role in the defense against infections and modulates tissue regeneration. In consideration of close proximity of NK cells and MSC at the site of injury we investigated if MSC could influence the ability of NK-cells to produce IFN-γ. Coculture experiments were performed with bone marrow-derived human MSC and human NK cells. MSC enhanced the ability of IL-12/IL-18-stimulated NK cells to secrete IFN-γin a dose-dependent manner. This activation of NK cells was dependent on cell-cell contact as well as on soluble factors. The increased IFN-γsecretion from NK cells after contact with MSC correlated with an increased level of intracellular IFN-γ. Alterations in the IL-12 signaling pathway including an increased expression of the IL-12β1 receptor subunit and an increased phosphorylation of signal transducer and activator of transcription 4 (STAT4) could be observed. In conclusion, MSC enhance the IFN-γrelease from NK cells which might improve the defense against infections at the site of injury but additionally might affect tissue regeneration.
机译:组织损伤诱导炎症反应,伴随着免疫细胞和间充质干细胞(MSC)的募集,从而有助于组织再生。用白介素-(IL-)12和IL-18刺激后,自然杀伤(NK)细胞分泌促炎性细胞因子干扰素-(IFN-)γ。 IFN-γ在抵抗感染和调节组织再生中起着至关重要的作用。考虑到NK细胞和MSC在损伤部位的紧密接近,我们研究了MSC是否可以影响NK细胞产生IFN-γ的能力。用骨髓来源的人MSC和人NK细胞进行共培养实验。 MSC增强了IL-12 / IL-18刺激的NK细胞以剂量依赖性方式分泌IFN-γ的能力。 NK细胞的激活取决于细胞与细胞之间的接触以及可溶性因子。与MSC接触后,NK细胞中IFN-γ分泌的增加与细胞内IFN-γ水平的增加有关。可以观察到IL-12信号传导途径的变化,包括IL-12β1受体亚基的表达增加以及信号转导子和转录激活子4(STAT4)的磷酸化增加。总之,MSC增强了NK细胞中IFN-γ的释放,这可能会增强对损伤部位感染的防御能力,但同时也可能影响组织再生。

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