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首页> 外文期刊>Biochemistry >EHD2 Interacts with the Insulin-Responsive Glucose Transporter (GLUT4) in Rat Adipocytes and May Participate in Insulin-Induced GLUT4 Recruitment
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EHD2 Interacts with the Insulin-Responsive Glucose Transporter (GLUT4) in Rat Adipocytes and May Participate in Insulin-Induced GLUT4 Recruitment

机译:EHD2与大鼠脂肪细胞中的胰岛素反应性葡萄糖转运蛋白(GLUT4)相互作用,并且可能参与胰岛素诱导的GLUT4募集。

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摘要

Insulin-induced GLUT4 recruitment to the plasma membrane involves GLUT4 trafficking through multiple subcellular compartments regulated by multiple proteins,many of which are yet to be identified.Here we describe a 65 kDa protein found in purified GLUT4 vesicles of rat adipocytes as a potential GLUT4 traffic regulatory protein.On the basis of MALDI-TOF MS,RT-PCR,gene cloning,protein sequencing,and immunoreactivity data,we identified this protein as EHD2,a member of the EH domain-containing proteins that have been implicated in vesicle trafficking.EHD2 in rat adipocytes was 85% membrane-associated,including approximately 10% in immunopurified GLUT4 vesicles.This association of EHD2 with GLUT4 vesicles occurred in PM and three distinct endosomal fractions and was not significantly affected by cellular insulin treatment.In co-immunoprecipitation experiments,however,EHD2 physically interacted with GLUT4 in each of these fractions,and cellular insulin treatment selectively enhanced this interaction in an endosomal fraction thought to contain GLUT4 exocytic vesicles.EHD2 also interacted with the clathrin adaptor middle chain subunit mu_1,mu_2,and rCALM in GST pull-down experiments.Significantly,an affinity-purified EHD2 antibody and a peptide corresponding to the EHD2 sequence Glu~(428)-Glu~(535) drastically (by 75% and 35%,respectively) suppressed the insulin-induced increase in the plasma membrane GLUT4 contents in SLO-permeabilized rat adipocytes without affecting the basal GLUT4 distribution.These findings strongly suggest that EHD2 interacts with GLUT4 in rat adipocytes and may play a key role in insulin-induced GLUT4 recruitment to the plasma membrane.
机译:胰岛素诱导的GLUT4募集到质膜涉及GLUT4通过受多种蛋白质调控的多个亚细胞区室的运输,其中许多尚待确定。在此,我们将在大鼠脂肪细胞的纯化GLUT4囊泡中发现的65 kDa蛋白质描述为潜在的GLUT4流量。根据MALDI-TOF MS,RT-PCR,基因克隆,蛋白测序和免疫反应性数据,我们将该蛋白鉴定为EHD2,它是与EH结构域相关的蛋白的一个成员,该蛋白与囊泡运输有关。大鼠脂肪细胞中EHD2的膜相关率为85%,其中免疫纯化的GLUT4囊泡中约为10%.EHD2与GLUT4囊泡的这种关系发生在PM和三个不同的内体组分中,并且不受细胞胰岛素治疗的明显影响。 ,但是,EHD2在其中每个部分中都与GLUT4发生了物理相互作用,而细胞胰岛素治疗选择性地增强了这种作用在GST下拉实验中,EHD2还与网格蛋白衔接子中间链亚基mu_1,mu_2和rCALM相互作用。EHD2还与网格蛋白衔接子中链亚基mu_1,mu_2和rCALM相互作用。重要的是,亲和纯化的EHD2抗体和对应于EHD2的肽序列Glu〜(428)-Glu〜(535)显着(分别为75%和35%)抑制了胰岛素诱导的SLO透化大鼠脂肪细胞中质膜GLUT4含量的增加,而没有影响基础GLUT4的分布。强烈建议EHD2与大鼠脂肪细胞中的GLUT4相互作用,并且可能在胰岛素诱导的GLUT4募集到质膜中起关键作用。

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