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Low-intensity pulsed ultrasound in combination with SonoVue induces cytotoxicity of human renal glomerular endothelial cells via repression of the ERK1/2 signaling pathway

机译:低强度脉冲超声与SonoVue联合通过抑制ERK1 / 2信号通路诱导人肾小球肾小管内皮细胞的细胞毒性

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摘要

>Objectives: Low-intensity pulsed ultrasound (LIPUS) and SonoVue have been used widely for diagnosis and therapeutic treatment. The effects of LIPUS and SonoVue on the microvascular system and underlying molecular mechanisms have not been established.>Methods: Cultured human renal glomerular endothelial cells (HRGECs) were treated with 5-min ultrasonic irradiation, 20% SonoVue or the combination of both treatments. Cell proliferation, viablity, and apoptosis were measured by MTT assay, Trypan blue exclusion assay and flow cytometry, respectively. Activation of extracellular regulated protein kinases (ERK) were examined by Western blot.>Results: We found that LIPUS and SonoVue alone do not induce cytotoxicity of HRGECs; however, the combination of the two treatments reduces cell proliferation and increases cell death. In addition, the combination of LIPUS and SonoVue suppressed the activation of ERK 1/2 in HRGRCs. With pretreatment of the inhibitor of ERK1/2 signaling, PD98059, LIPUS, and SonoVue does not induce additional cell death and inhibition of proliferation.>Conclusions: LIPUS combined with SonoVue induces cytotoxicity of HRGECs via repression of the ERK1/2 signaling pathway.
机译:>目标:低强度脉冲超声(LIPUS)和SonoVue已被广泛用于诊断和治疗。尚未确定LIPUS和SonoVue对微血管系统的影响及其潜在的分子机制。>方法:将培养的人肾小球内皮细胞(HRGEC)用5分钟超声照射,20%SonoVue或两种治疗方法的结合。通过MTT测定,锥虫蓝排除测定和流式细胞术分别测量细胞增殖,通透性和凋亡。 >结果:我们发现,单独的LIPUS和SonoVue不会诱导HRGECs的细胞毒性。但是,两种治疗方法的结合会降低细胞增殖并增加细胞死亡。此外,LIPUS和SonoVue的组合抑制了HRGRCs中ERK 1/2的活化。通过对ERK1 / 2信号抑制剂的预处理,PD98059,LIPUS和SonoVue不会诱导额外的细胞死亡和增殖抑制。>结论: LIPUS与SonoVue联合通过抑制ERK1诱导HRGEC的细胞毒性。 / 2信号通路。

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