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首页> 外文期刊>Journal of Ginseng Research >Protective effect of Korean Red Ginseng against FK506-induced damage in LLC-PK1 cells
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Protective effect of Korean Red Ginseng against FK506-induced damage in LLC-PK1 cells

机译:高丽红参对FK506诱导的LLC-PK1细胞损伤的保护作用

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Background Compound FK506 is an immunosuppressant agent that is frequently used to prevent rejection of solid organs upon transplant. However, nephrotoxicity due to apoptosis and inflammatory response mediated by FK506 limit its usefulness. In this study, the protective effect of Korean Red Ginseng (KRG) against FK506-induced damage in LLC-PK1 pig kidney epithelial cells was investigated. Methods LLC-PK1 cells were exposed to FK506 with KRG and cell viability was measured. Western blotting and RT-PCR analyses evaluated protein expression of MAPKs, caspase-3, and KIM-1. TLR-4 gene expression was assessed. Caspase-3 activities were also determined. The number of apoptotic cells was measured using an image-based cytometric assay. Results The reduction in LLC-PK1 cell viability by 60μM FK506 was recovered by KRG cotreatment in a dose-dependent manner. The phosphorylation of p38, p44/42 MAPKs (ERK), KIM-1, cleaved caspase-3, and TLR-4 mRNA expression was increased markedly in LLC-PK1 cells treated with 60μM FK506. However, with the exception of p-ERK, elevated levels of p-p38, KIM-1, cleaved caspase-3, and TLR-4 mRNA expression were significantly decreased after cotreatment with KRG. Activity level of caspase-3 was also attenuated by KRG cotreatment. Moreover, image-based cytometric assay showed that apoptotic cell death was increased by 60μM FK506 treatment, whereas it was decreased after cotreatment with KRG. Conclusion Taken together, these results suggest that the molecular mechanism of KRG in the FK506-induced nephrotoxicity may lead to the development of an adjuvant for the inhibition of adverse effect FK506 in the kidney.
机译:背景技术化合物FK506是一种免疫抑制剂,经常用于防止移植后实体器官的排斥。然而,由于FK506介导的细胞凋亡和炎性反应而引起的肾毒性限制了其用途。在这项研究中,研究了韩国红参(KRG)对FK506诱导的LLC-PK1猪肾上皮细胞损伤的保护作用。方法将LLC-PK1细胞与KRG一起暴露于FK506中,测定细胞活力。蛋白质印迹和RT-PCR分析评估了MAPK,caspase-3和KIM-1的蛋白表达。评估TLR-4基因表达。还确定了Caspase-3活性。使用基于图像的细胞计数测定法测量凋亡细胞的数目。结果通过KRG共处理以剂量依赖的方式恢复了60μMFK506使LLC-PK1细胞活力降低。在用60μMFK506处理的LLC-PK1细胞中,p38,p44 / 42 MAPKs(ERK),KIM-1,裂解的caspase-3和TLR-4 mRNA的磷酸化显着增加。但是,除p-ERK外,与KRG共同治疗后,p-p38,KIM-1,裂解的caspase-3和TLR-4 mRNA表达水平显着降低。 CRG协同处理也减弱了caspase-3的活性水平。此外,基于图像的细胞计数分析表明,凋亡细胞死亡通过60μMFK506处理增加,而在与KRG共同处理后减少。结论综上所述,这些结果表明KRG在FK506诱导的肾毒性中的分子机制可能导致开发抑制FK506在肾脏中的不良反应的佐剂。

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