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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Bone marrow ‐ mesenchymal stem cells impact on the U937 cells in the presence of staphylococcal enterotoxin B ( SEB SEB )
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Bone marrow ‐ mesenchymal stem cells impact on the U937 cells in the presence of staphylococcal enterotoxin B ( SEB SEB )

机译:骨髓 - 间充质干细胞在葡萄球菌肠毒素B(SEB SEB)存在下对U937细胞的影响

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Summary The growing resistance against conventional chemotherapy in acute myeloid leukemia ( AML ) is a noticeable clinical concern. Therefore, many researchers are looking for novel substances to overcome drug resistance in cancer. Staphylococcal enterotoxin B ( SEB ) is a superantigen ( SA g) and a promising compound which has lethal effects on malignant cells. In this unprecedented study, SEB was used against U937 cells in a co‐culture system in the presence of human bone marrow‐mesenchymal stem cells ( hBM ‐ MSC s). The effects of hBM ‐ MSC s on the proliferation and survival of U937 cell line with SEB was assessed using MTT assay and AnnexinV/ PI flowcytometry, respectively. Moreover, the expression of IL ‐6, IL ‐10, TGF ‐β, and inhibitor of nuclear factor kappa‐B kinase ( IKK b) was evaluated by real‐time PCR technique. The same experiments were also carried out using hBM ‐ MSC s‐conditioned medium ( hBM ‐ MSC s‐ CM ). The results showed that SEB reduced the proliferation and survival of U937 cell line, but hBM ‐ MSC s or hBM ‐ MSC s‐ CM suppressed the effects of SEB . Furthermore, real‐time PCR demonstrated that SEB could decrease the expression of IL ‐6, IL ‐10, and TGF ‐β in hBM ‐ MSC s ( P ??.05), while the production of IKK b was increased in comparison with the control group. These findings help us to have a broader understanding ofthe usage of SEB in the treatment of haematological malignancies, especially if it is targeted against hBM ‐ MSC s to disrupt their supportive effects on malignant cells.
机译:发明内容对急性髓鞘性白血病(AML)的常规化疗的巨大抗性是一个明显的临床关注。因此,许多研究人员正在寻找新的物质来克服癌症的耐药性。葡萄球菌肠毒素B(SEB)是一种超抗原(SA G)和具有对恶性细胞致命作用的有希望的化合物。在这个前所未有的研究中,在存在人骨髓间充质干细胞(HBM-MSC S)的存在下,SEB用于综合培养系统中的U937细胞。利用MTT测定和膜蛋白(Annexinv / Pi流胞流学评估HBM - MSC S对u937细胞系增殖和存活的影响。此外,通过实时PCR技术评价IL -6,IL -10,TGF-β和核因子Kappa-B激酶(IKK B)的抑制剂的表达。使用HBM-MSC S条件培养基(HBM - MSC S-CM)也进行相同的实验。结果表明,SEB降低了U937细胞系的增殖和存活,但HBM - MSC S或HBM-MSC S-CM抑制了SEB的效果。此外,实时PCR证明SEB可降低HBM-MSC S(P = 05)中IL-6,IL -10和TGF-β的表达,而IKK B的产生增加与对照组比较。这些发现有助于我们更广泛地了解SEB在治疗血液恶性恶性肿瘤中的使用,特别是如果它针对HBM - MSC的靶向,以破坏它们对恶性细胞的支持作用。

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