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P2Y11受体与P2Y1受体的异源寡聚化控制着P2Y11受体的内化和配体选择性。

Hetero-oligomerization of the P2Y11 receptor with the P2Y1 receptor controls the internalization and ligand selectivity of the P2Y11 receptor.

作者信息

Ecke Denise, Hanck Theodor, Tulapurkar Mohan E, Schäfer Rainer, Kassack Matthias, Stricker Rolf, Reiser Georg

机构信息

Institut für Neurobiochemie, Medizinische Fakultät, Otto-von-Guericke-Universität Magdeburg, Leipziger Str. 44, 39120 Magdeburg, Germany.

出版信息

Biochem J. 2008 Jan 1;409(1):107-16. doi: 10.1042/BJ20070671.

Abstract

Nucleotides signal through purinergic receptors such as the P2 receptors, which are subdivided into the ionotropic P2X receptors and the metabotropic P2Y receptors. The diversity of functions within the purinergic receptor family is required for the tissue-specificity of nucleotide signalling. In the present study, hetero-oligomerization between two metabotropic P2Y receptor subtypes is established. These receptors, P2Y1 and P2Y11, were found to associate together when co-expressed in HEK293 cells. This association was detected by co-pull-down, immunoprecipitation and FRET (fluorescence resonance energy transfer) experiments. We found a striking functional consequence of the interaction between the P2Y11 receptor and the P2Y1 receptor where this interaction promotes agonist-induced internalization of the P2Y11 receptor. This is remarkable because the P2Y11 receptor by itself is not able to undergo endocytosis. Co-internalization of these receptors was also seen in 1321N1 astrocytoma cells co-expressing both P2Y11 and P2Y1 receptors, upon stimulation with ATP or the P2Y1 receptor-specific agonist 2-MeS-ADP. 1321N1 astrocytoma cells do not express endogenous P2Y receptors. Moreover, in HEK293 cells, the P2Y11 receptor was found to functionally associate with endogenous P2Y1 receptors. Treatment of HEK293 cells with siRNA (small interfering RNA) directed against the P2Y1 receptor diminished the agonist-induced endocytosis of the heterologously expressed GFP-P2Y11 receptor. Pharmacological characteristics of the P2Y11 receptor expressed in HEK293 cells were determined by recording Ca2+ responses after nucleotide stimulation. This analysis revealed a ligand specificity which was different from the agonist profile established in cells expressing the P2Y11 receptor as the only metabotropic nucleotide receptor. Thus the hetero-oligomerization of the P2Y1 and P2Y11 receptors allows novel functions of the P2Y11 receptor in response to extracellular nucleotides.

摘要

核苷酸通过嘌呤能受体(如P2受体)发出信号,P2受体又可细分为离子型P2X受体和代谢型P2Y受体。嘌呤能受体家族功能的多样性是核苷酸信号传导组织特异性所必需的。在本研究中,确定了两种代谢型P2Y受体亚型之间的异源寡聚化。当在HEK293细胞中共表达时,发现这些受体P2Y1和P2Y11会相互结合。通过共下拉、免疫沉淀和FRET(荧光共振能量转移)实验检测到了这种结合。我们发现P2Y11受体与P2Y1受体之间相互作用产生了一个显著的功能结果,即这种相互作用促进了激动剂诱导的P2Y11受体内化。这很值得注意,因为P2Y11受体自身无法发生内吞作用。在用ATP或P2Y1受体特异性激动剂2-MeS-ADP刺激时,在共表达P2Y11和P2Y1受体的1321N1星形细胞瘤细胞中也观察到了这些受体的共同内化。1321N1星形细胞瘤细胞不表达内源性P2Y受体。此外,在HEK293细胞中,发现P2Y11受体与内源性P2Y1受体在功能上相关联。用针对P2Y受体的小干扰RNA(siRNA)处理HEK293细胞,可减少激动剂诱导的异源表达绿色荧光蛋白标记的P2Y11受体的内吞作用。通过记录核苷酸刺激后的Ca2+反应,确定了HEK293细胞中表达的P2Y11受体的药理学特性。该分析揭示了一种不同于在仅表达P2Y11受体作为唯一代谢型核苷酸受体的细胞中所确定的激动剂谱的配体特异性。因此,P2Y1和P2Y11受体的异源寡聚化使P2Y11受体能够响应细胞外核苷酸发挥新的功能。

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