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    李一鸣, 钱瑶瑶, 锁进猛, 虎亚男, 彭志勇. TIFA通过NF-κB信号通路调控焦亡对脓毒症急性肾损伤的影响[J]. 临床肾脏病杂志, 2022, 22(7): 584-589. DOI: 10.3969/j.issn.1671-2390.2022.07.009
    引用本文: 李一鸣, 钱瑶瑶, 锁进猛, 虎亚男, 彭志勇. TIFA通过NF-κB信号通路调控焦亡对脓毒症急性肾损伤的影响[J]. 临床肾脏病杂志, 2022, 22(7): 584-589. DOI: 10.3969/j.issn.1671-2390.2022.07.009
    Li Yi-ming, Qian Yao-yao, Suo Jin-meng, Hu Ya-nan, Peng Zhi-yong. Effect of TRAF-interacting protein with FHA domain-containing protein A on acute kidney injury during sepsis by regulating pyroptosis through NF-κB[J]. Journal of Clinical Nephrology, 2022, 22(7): 584-589. DOI: 10.3969/j.issn.1671-2390.2022.07.009
    Citation: Li Yi-ming, Qian Yao-yao, Suo Jin-meng, Hu Ya-nan, Peng Zhi-yong. Effect of TRAF-interacting protein with FHA domain-containing protein A on acute kidney injury during sepsis by regulating pyroptosis through NF-κB[J]. Journal of Clinical Nephrology, 2022, 22(7): 584-589. DOI: 10.3969/j.issn.1671-2390.2022.07.009

    TIFA通过NF-κB信号通路调控焦亡对脓毒症急性肾损伤的影响

    Effect of TRAF-interacting protein with FHA domain-containing protein A on acute kidney injury during sepsis by regulating pyroptosis through NF-κB

    • 摘要: 目的 探讨肿瘤坏死因子受体相关因子相互作用的具有叉形头相关结构域的蛋白(TRAF-interacting protein with FHA domain-containing protein A,TIFA)对肾小管上皮细胞焦亡的影响,以及是否通过核因子-κB(nuclear factor-κB,NF-κB)信号通路发挥作用。方法 收集重症监护病房12对脓毒症和诊断脓毒症后发生急性肾损伤(acute kidney injury,AKI)患者的血液标本,检测2组患者中血肌酐的含量和TIFA的含量。用TIFA siRNA敲低人肾小管上皮细胞中的TIFA,Toll样受体(toll-like receptor,TLR)4及TLR9激动剂刺激肾小管上皮细胞,蛋白质印迹法检测TIFA、Caspase-1、GSDMD表达,JC-1检测线粒体膜电位。采用盲肠结扎穿孔的方法构建脓毒症模型,小鼠腹腔注射TLR4抑制剂,检测小鼠肾脏组织病理、焦亡情况,观察脓毒症小鼠生存率。结果 脓毒症患者发生肾损伤后的尿液中TIFA增高。在肾小管上皮细胞中,敲低TIFA可抑制焦亡相关蛋白Caspase-1、GSDMD表达,减少炎症因子白细胞介素(interleukin,IL)-1β和IL-18产生,降低线粒体膜电位。在脓毒症AKI小鼠中,抑制TLR4信号通路可抑制TIFA和NF-κB,减少炎症因子IL-1β和IL-18产生,改善肾脏病理,提高脓毒症小鼠生存率。结论 在脓毒症AKI中TIFA可能通过抑制NF-κB信号通路降低焦亡发生,靶向TIFA的治疗可能是改善脓毒症AKI的有效方法。

       

      Abstract: Objective To explore the effect of TRAF-interacting protein with FHA domaincontaining protein A(TIFA)on pyroptosis of renal tubular epithelial cells and examine whether or not it operates through NF-κB signaling pathway. Methods Blood specimens were collected from 12 septic patients with acute kidney injury(AKI)in intensive care unit(ICU). The levels of creatinine and TIFA were measured. The expressions of TIFA,caspase-1 and GSDMD were detected by Western blot and mitochondrial membrane potential by JC-1. Septic model was established by cecal ligation and puncture and the mice received an intraperitoneal injection of TLR4 inhibitor for detecting renal injury and the expression of TIFA. Results Urinary TIFA rose after renal injury in septic patients. In renal tubular epithelial cells,a knockdown of TIFA could suppress the expressions of Caspase-1 and GSDMD and minimize the change of mitochondrial membrane potential. In septic AKI mice,an inhibition of TLR4 signaling pathway could suppress TIFA and NF-κB,reduce the production of inflammatory cytokines IL-1β and IL-18 and improve renal pathology and survival rate. Conclusion TIFA may reduce pyroptosis by inhibiting NF-κB signaling pathway in septic AKI. Targeted treatment of TIFA may improve septic AKI.

       

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