Chowdhury Helena H, Kreft Marko, Jensen Jørgen, Zorec Robert
Celica, Biomedical, Tehnološki park 24, 1000 Ljubljana, Slovenia.
Department of Physical Performance, Norwegian School of Sports Sciences, P.O. Box N-4014 Ullevål Stadion, 0806 Oslo, Norway.
Int J Mol Sci. 2014 Oct 2;15(10):17827-37. doi: 10.3390/ijms151017827.
Glucose is an important source of energy for mammalian cells and enters the cytosol via glucose transporters. It has been thought for a long time that glucose entering the cytosol is swiftly phosphorylated in most cell types; hence the levels of free glucose are very low, beyond the detection level. However, the introduction of new fluorescence resonance energy transfer-based glucose nanosensors has made it possible to measure intracellular glucose more accurately. Here, we used the fluorescent indicator protein (FLIPglu-600µ) to monitor cytosolic glucose dynamics in mouse 3T3-L1 cells in which glucose utilization for glycogen synthesis was inhibited. The results show that cells exhibit a low resting cytosolic glucose concentration. However, in cells with inhibited glycogen synthase activation, insulin induced a robust increase in cytosolic free glucose. The insulin-induced increase in cytosolic glucose in these cells is due to an imbalance between the glucose transported into the cytosol and the use of glucose in the cytosol. In untreated cells with sensitive glycogen synthase activation, insulin stimulation did not result in a change in the cytosolic glucose level. This is the first report of dynamic measurements of cytosolic glucose levels in cells devoid of the glycogen synthesis pathway.
葡萄糖是哺乳动物细胞重要的能量来源,通过葡萄糖转运蛋白进入细胞质。长期以来,人们一直认为,在大多数细胞类型中,进入细胞质的葡萄糖会迅速被磷酸化;因此,游离葡萄糖水平非常低,低于检测水平。然而,新型基于荧光共振能量转移的葡萄糖纳米传感器的出现,使得更准确地测量细胞内葡萄糖成为可能。在此,我们使用荧光指示剂蛋白(FLIPglu-600µ)来监测小鼠3T3-L1细胞中细胞质葡萄糖的动态变化,其中糖原合成的葡萄糖利用受到抑制。结果表明,细胞呈现出较低的静息细胞质葡萄糖浓度。然而,在糖原合酶激活受到抑制的细胞中,胰岛素诱导细胞质游离葡萄糖显著增加。这些细胞中胰岛素诱导的细胞质葡萄糖增加,是由于转运到细胞质中的葡萄糖与细胞质中葡萄糖的利用之间失衡所致。在糖原合酶激活敏感的未处理细胞中,胰岛素刺激并未导致细胞质葡萄糖水平发生变化。这是关于缺乏糖原合成途径的细胞中细胞质葡萄糖水平动态测量的首次报道。