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Release of Cytokines from Human Umbilical Vein Endothelial Cells Treated with Platinum Compounds in vitro

机译:铂化合物体外处理后从人脐静脉内皮细胞释放细胞因子

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摘要

Endothelial cells (EC) produce cytokines, such as interleukin (IL)‐1, IL‐6, IL‐8 and granulocyte‐macrophage colony‐stimulating factor (GM‐CSF). These cytokines have an important role in the proliferation and differentiation of hematopoietic progenitor cells. On the other hand, anticancer agents generally cause hematopoietic disorders. However, little is known about the effects of chemotherapeutic agents on the secretion of cytokines from EC. Therefore, we investigated if treatment with platinum compounds may stimulate EC to secrete cytokines. EC newly isolated from a human umbilical vein were exposed to cisplatin, carboplatin, or TRK‐710 for 80 min, then the cells were washed and placed in fresh medium. The levels of cytokines in the fresh medium were measured by the ELISA method, the levels of intracellular hydrogen peroxide (H2O2) were measured by flow cytometry, and the rhodamine 123‐stained live mitochondria of the EC were observed under a confocal laser microscope. Platinum compounds induced cytokine production in human EC: cisplatin most prominently induced the release of IL‐1 and IL‐6, and TRK‐710 had the greatest ability to induce the release of GM‐CSF. Intracellular H2O2 production and IL‐8 release were transiently induced immediately after treatment with platinum compounds, leading to IL‐1 release when H2O2 production was eliminated. These results may provide new insights into the hematological toxicity induced by anticancer agents and the role of IL‐1 and IL‐6 secreted from EC in this toxicity.
机译:内皮细胞(EC)产生细胞因子,例如白介素(IL)-1,IL-6,IL-8和粒细胞巨噬细胞集落刺激因子(GM-CSF)。这些细胞因子在造血祖细胞的增殖和分化中具有重要作用。另一方面,抗癌剂通常引起造血疾病。然而,关于化学治疗剂对EC分泌细胞因子的影响知之甚少。因此,我们调查了用铂化合物治疗是否可以刺激EC分泌细胞因子。将新从人脐静脉分离出的EC暴露于顺铂,卡铂或TRK-710中80分钟,然后洗涤细胞并将其置于新鲜培养基中。通过ELISA方法测量新鲜培养基中的细胞因子水平,通过流式细胞仪测量细胞内过氧化氢(H2O2)水平,并在共聚焦激光显微镜下观察EC的若丹明123染色的活线粒体。铂化合物诱导人EC中细胞因子的产生:顺铂最主要地诱导IL-1和IL-6的释放,而TRK-710具有最大的诱导GM-CSF释放的能力。用铂类化合物处理后立即瞬时诱导细胞内H2O2的产生和IL-8的释放,当消除H2O2的产生时导致IL-1的释放。这些结果可能为抗癌药引起的血液学毒性以及EC分泌的IL-1和IL-6在这种毒性中的作用提供新的见解。

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