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Calcium oxalate crystals induces tight junction disruption in distal renal tubular epithelial cells by activating ROS/Akt/p38 MAPK signaling pathway

机译:草酸钙晶体通过激活ROS / AKT / P38 MAPK信号通路诱导远端肾小管上皮细胞中的紧密结突发

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摘要

Tight junction plays important roles in regulating paracellular transports and maintaining cell polarity. Calcium oxalate monohydrate (COM) crystals, the major crystalline composition of kidney stones, have been demonstrated to be able to cause tight junction disruption to accelerate renal cell injury. However, the cellular signaling involved in COM crystal-induced tight junction disruption remains largely to be investigated. In the present study, we proved that COM crystals induced tight junction disruption by activating ROS/Akt/p38 MAPK pathway. Treating Madin-Darby canine kidney (MDCK) cells with COM crystals induced a substantial increasing of ROS generation and activation of Akt that triggered subsequential activation of ASK1 and p38 mitogen-activated protein kinase (MAPK). Western blot revealed a significantly decreased expression of ZO-1 and occludin, two important structural proteins of tight junction. Besides, redistribution and dissociation of ZO-1 were observed by COM crystals treatment. Inhibition of ROS by N-acetyl-l-cysteine (NAC) attenuated the activation of Akt, ASK1, p38 MAPK, and down-regulation of ZO-1 and occludin. The redistribution and dissociation of ZO-1 were also alleviated by NAC treatment. These results indicated that ROS were involved in the regulation of tight junc-
机译:紧密交界处在调节术晶间运输和维持电池极性方面发挥重要作用。已经证明了草酸钙一水合物(COM)晶体,肾结石的主要晶体组成,以造成紧密的结粘连以加速肾细胞​​损伤。然而,涉及COM晶体诱导的紧密接线破坏的细胞信号仍然在很大程度上被研究。在本研究中,我们证明COM晶体通过激活ROS / AKT / P38 MAPK途径诱导紧密结扰。用COM晶体治疗Madin-Darby犬肾(MDCK)细胞诱导AKT的ROS生成和激活的显着增加,该Akt引发了Ask1和P38丝裂型蛋白激酶(MAPK)的后续激活。 Western印迹显示出显着降低的ZO-1和occludin表达,紧密结合的两个重要结构蛋白。此外,通过COM晶体处理观察到ZO-1的再分配和解离。 N-乙酰基-1-半胱氨酸(NAC)抑制ROS(NAC)衰减AKT,ASK1,P38 MAPK和ZO-1和occludin的下调的活化。通过NAC治疗还减轻了ZO-1的再分配和解离。这些结果表明,ROS参与了严格的JUNC-

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