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一种与磷脂酶C和腺苷酸环化酶偶联的人嘌呤能P2Y受体的克隆。

Cloning of a human purinergic P2Y receptor coupled to phospholipase C and adenylyl cyclase.

作者信息

Communi D, Govaerts C, Parmentier M, Boeynaems J M

机构信息

Institute of Interdisciplinary Research, School of Medicine, Erasme Hospital, Université Libre de Bruxelles, 1070 Brussels, Belgium.

出版信息

J Biol Chem. 1997 Dec 19;272(51):31969-73. doi: 10.1074/jbc.272.51.31969.

Abstract

Clones encoding a new human P2Y receptor, provisionally called P2Y11, have been isolated from human placenta complementary DNA and genomic DNA libraries. The 1113-base pair open reading frame is interrupted by one intron. The P2Y11 receptor is characterized by considerably larger second and third extracellular loops than the subtypes described so far. The deduced amino acid sequence exhibits 33% amino acid identity with the P2Y1 receptor, its closest homolog. Northern blot analysis detected human P2Y11 receptor messenger RNA in spleen and HL-60 cells. The level of P2Y11 transcripts was strongly increased in these cells after granulocyte differentiation induced by retinoic acid or dimethyl sulfoxide. The new receptor was stably expressed in 1321N1 astrocytoma and CHO-K1 cells, where it couples to the stimulation of both the phosphoinositide and adenylyl cyclase pathways, a unique feature among the P2Y family. The rank order of agonists potency was: ATP > 2-methylthio-ATP >>> ADP, whereas UTP and UDP were inactive, indicating that it behaves as a selective purinoceptor.

摘要

已从人胎盘互补DNA和基因组DNA文库中分离出编码一种新的人P2Y受体(暂称为P2Y11)的克隆。1113个碱基对的开放阅读框被一个内含子中断。P2Y11受体的特征是其第二和第三细胞外环比目前描述的亚型大得多。推导的氨基酸序列与最接近的同源物P2Y1受体具有33%的氨基酸同一性。Northern印迹分析在脾脏和HL-60细胞中检测到人P2Y11受体信使RNA。在用视黄酸或二甲基亚砜诱导粒细胞分化后,这些细胞中P2Y11转录本的水平显著增加。新受体在1321N1星形细胞瘤细胞和CHO-K1细胞中稳定表达,在这些细胞中它与磷酸肌醇和腺苷酸环化酶途径的刺激偶联,这是P2Y家族中的一个独特特征。激动剂效力的顺序为:ATP > 2-甲硫基-ATP >>> ADP,而UTP和UDP无活性,表明它表现为一种选择性嘌呤受体。

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