首页> 美国卫生研究院文献>Cell Regulation >GLUT4 Is Sorted to Vesicles Whose Accumulation Beneath and Insertion into the Plasma Membrane Are Differentially Regulated by Insulin and Selectively Affected by Insulin Resistance
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GLUT4 Is Sorted to Vesicles Whose Accumulation Beneath and Insertion into the Plasma Membrane Are Differentially Regulated by Insulin and Selectively Affected by Insulin Resistance

机译:GLUT4被归类为囊泡囊泡的下面和血浆膜中的积累受到胰岛素的差异调节并受到胰岛素抵抗的影响

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摘要

Insulin stimulates glucose transport by recruiting the GLUT4 glucose transporter to the plasma membrane. Here we use total internal reflection fluorescence microscopy to show that two trafficking motifs of GLUT4, a FQQI motif and a TELE-based motif, target GLUT4 to specialized vesicles that accumulate adjacent to the plasma membrane of unstimulated adipocytes. Mutations of these motifs redistributed GLUT4 to transferrin-containing recycling vesicles adjacent to the plasma membrane, and the degree of redistribution correlated with the increases of the GLUT4 mutants in the plasma membrane of basal adipocytes. These results establish that GLUT4 defaults to recycling endosomes when trafficking to specialized vesicles is disrupted, supporting the hypothesis that the specialized vesicles are derived from an endosomal compartment. Insulin stimulates both the accumulation of GLUT4 in the evanescent field and the fraction of this GLUT4 that is inserted into the plasma membrane. Unexpectedly, these two steps are differentially affected by the development of insulin resistance. We ascribe this selective insulin resistance to inherent differences in the sensitivities of GLUT4 vesicle accumulation and insertion into the plasma membrane to insulin. Differences in insulin sensitivities of various processes may be a general mechanism for the development of the physiologically important phenomenon of selective insulin resistance.
机译:胰岛素通过将GLUT4葡萄糖转运蛋白募集到质膜来刺激葡萄糖转运。在这里,我们使用全内反射荧光显微镜术来显示GLUT4的两个运输基序,一个FQQI基序和一个基于TELE的基序,将GLUT4靶向到与未刺激的脂肪细胞的质膜相邻堆积的专门囊泡。这些基序的突变将GLUT4重新分布到邻近质膜的含运铁蛋白的回收囊泡中,并且重新分布的程度与基础脂肪细胞质膜中GLUT4突变的增加相关。这些结果表明,当转运至特定囊泡时,GLUT4默认无法回收内体,这支持了特定囊泡源自内体区室的假设。胰岛素既可以刺激衰老场中GLUT4的积累,又可以刺激GLUT4插入质膜的部分。出乎意料的是,这两个步骤受胰岛素抵抗发展的影响不同。我们将这种选择性胰岛素抵抗归因于GLUT4囊泡积聚和插入质膜中对胰岛素的敏感性固有的差异。各种过程中胰岛素敏感性的差异可能是选择性胰岛素抵抗的重要生理现象发展的一般机制。

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