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秦誉宁, 姚宇豪, RUBAYIZA Joshua, 何书英. 肝素寡糖抑制CoCl2诱导的HUVEC细胞糖酵解及其机制[J]. 中国药科大学学报, 2023, 54(5): 626-633. DOI: 10.11665/j.issn.1000-5048.2023042501
引用本文: 秦誉宁, 姚宇豪, RUBAYIZA Joshua, 何书英. 肝素寡糖抑制CoCl2诱导的HUVEC细胞糖酵解及其机制[J]. 中国药科大学学报, 2023, 54(5): 626-633. DOI: 10.11665/j.issn.1000-5048.2023042501
QIN Yuning, YAO Yuhao, RUBAYIZA Joshua, HE Shuying. Inhibition of CoCl2-induced glycolysis in HUVEC cells by heparin-derived oligosaccharides and its mechanism[J]. Journal of China Pharmaceutical University, 2023, 54(5): 626-633. DOI: 10.11665/j.issn.1000-5048.2023042501
Citation: QIN Yuning, YAO Yuhao, RUBAYIZA Joshua, HE Shuying. Inhibition of CoCl2-induced glycolysis in HUVEC cells by heparin-derived oligosaccharides and its mechanism[J]. Journal of China Pharmaceutical University, 2023, 54(5): 626-633. DOI: 10.11665/j.issn.1000-5048.2023042501

肝素寡糖抑制CoCl2诱导的HUVEC细胞糖酵解及其机制

Inhibition of CoCl2-induced glycolysis in HUVEC cells by heparin-derived oligosaccharides and its mechanism

  • 摘要: 以CoCl2刺激人脐静脉内皮细胞(HUVEC)建立细胞异常缺氧损伤模型,探究肝素寡糖(HDO)对HUVEC细胞中糖酵解的影响及分子机制。实验分为对照组(无血清DMEM培养基)、模型组(无血清DMEM培养基+50 μmol/L CoCl2)及HDO给药组(模型组基础上分别添加0.01、0.1、1 μmol/L HDO)。采用生化试剂盒检测HDO对HUVEC细胞葡萄糖摄取及乳酸积累的影响;采用Western blot及qPCR实验检测HIF-1α、GLUT-1及LDHA基因转录和蛋白表达的影响,并对PI3K/Akt信号通路进行检测。结果显示:HDO可以抑制HUVEC细胞的葡萄糖摄取及乳酸生成,下调HIF-1α、GLUT-1及LDHA的表达水平,影响PI3K/Akt信号通路的激活。结果表明,HDO可以通过抑制PI3K/Akt/HIF-1α信号轴的激活从而调控HUVEC细胞的糖酵解水平。

     

    Abstract: In this paper, cobalt chloride was used to stimulate human umbilical vein endothelial cells (HUVEC) to establish a model of abnormal hypoxic injury, to investigate the effect of heparin-derived oligosaccharides (HDO) on glycolysis in HUVEC cells and its molecular mechanism.The experiment was divided into the control group (FBS-free DMEM medium), the model group (FBS-free DMEM medium +50 μmol/L CoCl2), and the HDO group (modeling+0.01, 0.1, 1 μmol/L HDO).Firstly, a biochemical kit was used to detect the effects of HDO on glucose uptake and lactic acid accumulation in HUVEC cells, then Western blot and qPCR were used to detect the effects of HIF-1α, GLUT-1 and LDHA gene transcription and protein expression, and finally, PI3K/Akt signaling pathway was detected.The results showed that HDO inhibited glucose uptake and lactate production, down-regulated the expression of HIF-1α, GLUT-1, and LDHA, and affected the activation of the PI3K/Akt signaling pathway.HDO could regulate the glycolysis level of HUVEC cells by inhibiting the activation of the PI3K/Akt/HIF-1α signaling axis.

     

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