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首页> 外文期刊>FEBS Letters >Analyses of the co‐localization of cellubrevin and the GLUT4 glucose transporter in rat and human insulin‐responsive tissues
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Analyses of the co‐localization of cellubrevin and the GLUT4 glucose transporter in rat and human insulin‐responsive tissues

机译:在大鼠和人类胰岛素反应性组织中纤维尿素和GLUT4葡萄糖转运蛋白的共定位分析

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>We have investigated the subcellular distribution and association of cellubrevin, a low molecular weight protein implicated in the process of membrane fusion, with intracellular membranes containing the insulin-sensitive GLUT4 glucose transporter from rat adipocytes, rat skeletal muscle and human skeletal muscle. SDS-PAGE and immunoblot analyses of subcellular fractions of adipocytes and skeletal muscle indicated a positive correlation between the distribution of GLUT4 and cellubrevin in intracellular membrane fractions tested from all tissues. The identity of the polypeptide reacting with antiserum against cellubrevin was further confirmed on the basis of its susceptibility to proteolysis by tetanus toxin. Immunoisolation of GLUT4-containing vesicles from a microsomal fraction enriched with GLUT4 and cellubrevin revealed that cellubrevin could be coprecipitated with GLUT4 vesicles from adipocytes. In contrast, intracellular GLUT4 vesicles isolated from both rat and human skeletal muscle were devoid of any detectable immunoreactivity towards cellubrevin. The observation that cellubrevin does not colocalise with intracellular GLUT4 in skeletal muscle from two different species, rat and human, would strongly suggest that it is unlikely to participate in the insulininduced delivery of GLUT4 to the cell surface in skeletal muscle.
机译:>我们已经研究了纤维微蛋白的亚细胞分布和缔合,纤维微蛋白是一种与膜融合过程有关的低分子量蛋白,其细胞内膜含有来自大鼠脂肪细胞,大鼠骨骼肌和人骨骼肌的胰岛素敏感性GLUT4葡萄糖转运蛋白。 SDS-PAGE和对脂肪细胞和骨骼肌亚细胞部分的免疫印迹分析表明,从所有组织测试的细胞内膜部分中GLUT4和Cellubrevin的分布呈正相关。基于其对破伤风毒素的蛋白水解敏感性,进一步证实了与抗纤维尿素抗血清反应的多肽的身份。从富含GLUT4和Cellubrevin的微粒体部分中对GLUT4囊泡进行免疫分离显示,Cellubrevin可以与来自脂肪细胞的GLUT4囊泡共沉淀。相反,从大鼠和人骨骼肌中分离的细胞内GLUT4囊泡对纤维蛋白没有任何可检测的免疫反应性。 Cellubrevin不能与大鼠和人类这两个不同物种的骨骼肌中的细胞内GLUT4共定位的观察结果强烈表明,它不太可能参与胰岛素诱导的GLUT4传递至骨骼肌细胞表面。

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