Department of Nephrology, The Children's Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang 310003, P.R. China.
Mol Med Rep. 2017 Aug;16(2):1465-1471. doi: 10.3892/mmr.2017.6753. Epub 2017 Jun 12.
The present study was performed to investigate the effect of Huaiqihuang (HQH) on hyperglycemia (HG)-induced mitochondrial dysfunction and endoplasmic reticulum (ER) stress in MPC5 podocytes. The effects of HQH and HG on cell viability were assessed using an MTT assay. mRNA and protein expression levels were evaluated using reverse transcription-quantitative polymerase chain reaction and western blot analysis, respectively. Cell apoptosis was assessed using terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling, whereas reactive oxygen species production and alterations in mitochondrial membrane potential were assessed using flow cytometry. DNA damage was evaluated using a comet assay. The results demonstrated that treatment of podocytes with HQH markedly suppressed the HG‑induced generation of reactive oxygen species. HQH also significantly improved mitochondrial membrane potential in podocytes exposed to HG. When the podocytes were treated with HG, Ca2+ levels were significantly increased, compared with those in the control group, whereas treatment of the podocytes with HQH significantly reversed the HG‑induced upregulation of Ca2+ secretion. Treatment of the podocytes with HQH significantly reversed the HG‑induced upregulation of glucose‑related protein 78 (GRP78) and C/EBP‑homologous protein, which were used as indicators of ER stress. Furthermore, GRP78 loss‑of‑function attenuated HG‑induced podocyte dysfunction, including cell apoptosis and DNA damage. In conclusion, beneficial effects of HQH on HG‑induced MPC5 podocyte dysfunction were observed, and occurred through the suppression of mitochondrial dysfunction and ER stress.
本研究旨在探讨槐杞黄(HQH)对高血糖(HG)诱导的 MPC5 足细胞线粒体功能障碍和内质网(ER)应激的影响。通过 MTT 测定法评估 HQH 和 HG 对细胞活力的影响。通过逆转录定量聚合酶链反应和 Western blot 分析分别评估 mRNA 和蛋白质表达水平。通过末端脱氧核苷酸转移酶脱氧尿苷三磷酸缺口末端标记法评估细胞凋亡,而通过流式细胞术评估活性氧(ROS)的产生和线粒体膜电位的变化。通过彗星试验评估 DNA 损伤。结果表明,HQH 处理足细胞可显著抑制 HG 诱导的 ROS 产生。HQH 还可显著改善 HG 暴露的足细胞中线粒体膜电位。当足细胞用 HG 处理时,与对照组相比,Ca2+水平显著增加,而 HQH 处理可显著逆转 HG 诱导的 Ca2+分泌上调。HQH 处理可显著逆转 HG 诱导的葡萄糖相关蛋白 78(GRP78)和 C/EBP 同源蛋白的上调,这两种蛋白被用作 ER 应激的指标。此外,GRP78 功能丧失可减弱 HG 诱导的足细胞功能障碍,包括细胞凋亡和 DNA 损伤。总之,HQH 对 HG 诱导的 MPC5 足细胞功能障碍具有有益作用,其机制是通过抑制线粒体功能障碍和 ER 应激。