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扩充性血液透析疗法通过调节 VEGF、TNF-α 和 AP-1 信号改善尿毒症引起的全身微炎症和内皮功能障碍。

Expanded Hemodialysis Therapy Ameliorates Uremia-Induced Systemic Microinflammation and Endothelial Dysfunction by Modulating VEGF, TNF-α and AP-1 Signaling.

机构信息

Department of Nephrology and Internal Intensive Care Medicine, Charité Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), Berlin, Germany.

BIH Center for Regenerative Therapies (BCRT), Charité Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), Berlin, Germany.

出版信息

Front Immunol. 2021 Nov 11;12:774052. doi: 10.3389/fimmu.2021.774052. eCollection 2021.

Abstract

ABSTRACT

Systemic chronic microinflammation and altered cytokine signaling, with adjunct cardiovascular disease (CVD), endothelial maladaptation and dysfunction is common in dialysis patients suffering from end-stage renal disease and associated with increased morbidity and mortality. New hemodialysis filters might offer improvements. We here studied the impact of novel improved molecular cut-off hemodialysis filters on systemic microinflammation, uremia and endothelial dysfunction. Human endothelial cells (ECs) were incubated with uremic serum obtained from patients treated with two different hemodialysis regimens in the Permeability Enhancement to Reduce Chronic Inflammation (PERCI-II) crossover clinical trial, comparing High-Flux (HF) and Medium Cut-Off (MCO) membranes, and then assessed for their vascular endothelial growth factor (VEGF) production and angiogenesis. Compared to HF membranes, dialysis with MCO membranes lead to a reduction in proinflammatory mediators and reduced endothelial VEGF production and angiogenesis. Cytokine multiplex screening identified tumor necrosis factor (TNF) superfamily members as promising targets. The influence of TNF-α and its soluble receptors (sTNF-R1 and sTNF-R2) on endothelial VEGF promoter activation, protein release, and the involved signaling pathways was analyzed, revealing that this detrimental signaling was indeed induced by TNF-α and mediated by AP-1/c-FOS signaling. In conclusion, uremic toxins, in particular TNF-signaling, promote endothelial maladaptation, VEGF expression and aberrant angiogenesis, which can be positively modulated by dialysis with novel MCO membranes.

TRANSLATIONAL PERSPECTIVE AND GRAPHICAL ABSTRACT

Systemic microinflammation, altered cytokine signaling, cardiovascular disease, and endothelial maladaptation/dysfunction are common clinical complications in dialysis patients suffering from end-stage renal disease. We studied the impact of novel improved medium-cut-off hemodialysis filters on uremia and endothelial dysfunction. We can show that uremic toxins, especially TNF-signaling, promote endothelial maladaptation, VEGF expression and aberrant angiogenesis, which can be positively modulated by dialysis with novel improved medium-cut-off membranes.

摘要

摘要

患有终末期肾病的透析患者常伴有全身慢性微炎症和细胞因子信号改变,以及并发的心血管疾病、血管内皮适应不良和功能障碍,这些并发症与发病率和死亡率的增加有关。新型血液透析滤过器可能会有所改善。本研究旨在探讨新型改良的分子截留血液透析滤过器对全身微炎症、尿毒症和血管内皮功能障碍的影响。将尿毒症患者的尿毒症血清与两种不同血液透析方案(Permeability Enhancement to Reduce Chronic Inflammation 交叉临床试验中的高通量(HF)和中分子截留(MCO)膜)处理的患者的尿毒症血清一起孵育,然后评估其血管内皮生长因子(VEGF)的产生和血管生成。与 HF 膜相比,MCO 膜透析可减少促炎介质,降低内皮 VEGF 的产生和血管生成。细胞因子多重筛选确定肿瘤坏死因子(TNF)超家族成员是有前途的靶点。分析 TNF-α及其可溶性受体(sTNF-R1 和 sTNF-R2)对血管内皮 VEGF 启动子激活、蛋白释放及相关信号通路的影响,结果表明,这种有害信号确实是由 TNF-α诱导的,由 AP-1/c-FOS 信号介导。结论:尿毒症毒素,特别是 TNF 信号,可促进血管内皮适应不良、VEGF 表达和异常血管生成,新型 MCO 膜透析可正向调节这些改变。

翻译视角和图表摘要

全身微炎症、细胞因子信号改变、心血管疾病和血管内皮适应不良/功能障碍是患有终末期肾病的透析患者的常见临床并发症。我们研究了新型改良中分子截留血液透析滤过器对尿毒症和血管内皮功能障碍的影响。我们可以表明,尿毒症毒素,特别是 TNF 信号,可促进血管内皮适应不良、VEGF 表达和异常血管生成,新型改良中分子截留膜透析可正向调节这些改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da2a/8632537/a277be659615/fimmu-12-774052-g007.jpg

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