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The neuronal Ca2+-binding protein 2 (NECAB2) interacts with the adenosine A(2A) receptor and modulates the cell surface expression and function of the receptor

机译:神经元Ca2 +结合蛋白2(NECAB2)与腺苷A(2A)受体相互作用,并调节该受体的细胞表面表达和功能

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Heptaspanning membrane also known as G protein-coupled receptors (GPCR) do interact with a variety of intracellular proteins whose function is regulate receptor traffic and/or signaling. Using a yeast two-hybrid screen, NECAB2, a neuronal calcium binding protein, was identified as a binding partner for the adenosine A(2A) receptor (A(2A)R) interacting with its C-terminal domain. Co-localization, co-immunoprecipitation and pull-down experiments showed a close and specific interaction between A2AR and NECAB2 in both transfected HEK-293 cells and also in rat striatum. Immunoclectron microscopy detection of NECAB2 and A2AR in the rat striatopallidall structures indicated that both proteins are co-distributed in the same glutamatergic nerve terminals. The interaction of NECAB2 with A2AR modulated the cell surface expression, the ligand-dependent internalization and the receptor-mediated activation of the MAPK pathway. Overall, these results show that A2AR interacts with NECAB2 in striatal neurones co-expressing the two proteins and that the interaction is relevant for A(2A)R function. (c) 2007 Elsevier Inc. All rights reserved.
机译:庚烷膜也称为G蛋白偶联受体(GPCR)确实与多种细胞内蛋白相互作用,其功能是调节受体的运输和/或信号传导。使用酵母双杂交筛选,NECAB2,一种神经元钙结合蛋白,被确定为与其C末端域相互作用的腺苷A(2A)受体(A(2A)R)的结合伴侣。共同定位,共同免疫沉淀和下拉实验表明,在转染的HEK-293细胞和大鼠纹状体中,A2AR和NECAB2之间都有密切而特异性的相互作用。免疫电镜检测到的大鼠纹状体allallall结构中的NECAB2和A2AR表明,这两种蛋白共同分布在相同的谷氨酸能神经末梢。 NECAB2与A2AR的相互作用调节了细胞表面表达,配体依赖性内在化和MAPK途径的受体介导的活化。总体而言,这些结果表明,A2AR与共表达两种蛋白质的纹状体神经元中的NECAB2相互作用,并且该相互作用与A(2A)R功能有关。 (c)2007 Elsevier Inc.保留所有权利。

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