穿心莲内酯通过PKC途径促进L6细胞的葡萄糖摄取和GLUT4运输。

Jingya Liao, Ziwei Yang, Yanhong Yao, Xinzhou Yang, Jinhua Shen, Ping Zhao
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摘要

葡萄糖转运蛋白4 (GLUT4)是一种调节血糖平衡的膜蛋白,与2型糖尿病密切相关。穿心莲内酯是一种从中药穿心莲中提取的二萜内酯,具有多种生物活性。本研究探讨AND对L6细胞的降糖作用及其机制。葡萄糖测定试剂盒检测L6细胞对葡萄糖的摄取。Western blot检测GLUT4的表达和蛋白激酶B (PKB/Akt)、amp依赖性蛋白激酶(AMPK)、蛋白激酶C (PKC)的磷酸化水平。同时,用激光共聚焦扫描显微镜检测myc-GLUT4-mOrange-L6细胞内Ca2+水平和GLUT4易位。结果表明,AND增强了L6细胞对葡萄糖的摄取、GLUT4的表达及与质膜的融合。同时,AND还显著激活AMPK和PKC的磷酸化,增加细胞内Ca2+的浓度。and诱导的GLUT4表达被PKC抑制剂显著抑制(Gö6983)。此外,在0 mM胞外Ca2+和0 mM胞外Ca2+ + 10 μM BAPTA-AM(胞内Ca2+螯合剂)的情况下,and诱导GLUT4易位,并显著抑制葡萄糖的摄取。因此,我们得出结论,AND通过PKC途径以Ca2+依赖的方式促进L6细胞中GLUT4的表达及其与质膜的融合,从而增加葡萄糖的摄取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Andrographolide Promotes Uptake of Glucose and GLUT4 Transport through the PKC Pathway in L6 Cells.

Andrographolide Promotes Uptake of Glucose and GLUT4 Transport through the PKC Pathway in L6 Cells.

Andrographolide Promotes Uptake of Glucose and GLUT4 Transport through the PKC Pathway in L6 Cells.

Andrographolide Promotes Uptake of Glucose and GLUT4 Transport through the PKC Pathway in L6 Cells.

Glucose transporter 4 (GLUT4) is a membrane protein that regulates blood glucose balance and is closely related to type 2 diabetes. Andrographolide (AND) is a diterpene lactone extracted from herbal medicine Andrographis paniculata, which has a variety of biological activities. In this study, the antidiabetic effect of AND in L6 cells and its mechanism were investigated. The uptake of glucose of L6 cells was detected by a glucose assay kit. The expression of GLUT4 and phosphorylation of protein kinase B (PKB/Akt), AMP-dependent protein kinase (AMPK), and protein kinase C (PKC) were detected by Western blot. At the same time, the intracellular Ca2+ levels and GLUT4 translocation in myc-GLUT4-mOrange-L6 cells were detected by confocal laser scanning microscopy. The results showed that AND enhanced the uptake of glucose, GLUT4 expression and fusion with plasma membrane in L6 cells. Meanwhile, AND also significantly activated the phosphorylation of AMPK and PKC and increased the concentration of intracellular Ca2+. AND-induced GLUT4 expression was significantly inhibited by a PKC inhibitor (Gö6983). In addition, in the case of 0 mM extracellular Ca2+ and 0 mM extracellular Ca2+ + 10 μM BAPTA-AM (intracellular Ca2+ chelator), AND induced the translocation of GLUT4, and the uptake of glucose was significantly inhibited. Therefore, we concluded that AND promoted the expression of GLUT4 and its fusion with plasma membrane in L6 cells through PKC pathways in a Ca2+-dependent manner, thereby increasing the uptake of glucose.

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