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新型钙离子动员信使烟酰胺腺嘌呤二核苷酸磷酸的结合位点在大脑中的广泛分布。

Widespread distribution of binding sites for the novel Ca2+-mobilizing messenger, nicotinic acid adenine dinucleotide phosphate, in the brain.

作者信息

Patel S, Churchill G C, Sharp T, Galione A

机构信息

Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, United Kingdom.

出版信息

J Biol Chem. 2000 Nov 24;275(47):36495-7. doi: 10.1074/jbc.C000458200.

Abstract

Nicotinic acid adenine dinucleotide phosphate (NAADP) is a potent Ca(2+)-mobilizing agent in invertebrate eggs that has recently been shown to be active in certain mammalian and plant systems. Little, however, is known concerning the properties of putative NAADP receptors. Here, for the first time, we report binding sites for NAADP in brain. In contrast to sea urchin egg homogenates, [(32)P]NAADP bound reversibly to multiple sites in brain membranes. The rank order of potency of NAADP, 2',3'-cyclic NAADP and 3'-NAADP in displacing [(32)P]NAADP was, however, the same in the two systems and in agreement with their ability to mobilize Ca(2+) from homogenates. These data indicate that [(32)P]NAADP likely binds to receptors mediating Ca(2+) mobilization. Autoradiography revealed striking heterogeneity in the distribution of [(32)P]NAADP binding sites throughout the brain. Our data strongly support a role for NAADP-induced Ca(2+) signaling in the brain.

摘要

烟酰胺腺嘌呤二核苷酸磷酸(NAADP)是一种在无脊椎动物卵中具有强大钙离子动员能力的物质,最近已证明它在某些哺乳动物和植物系统中也具有活性。然而,关于假定的NAADP受体的特性却知之甚少。在此,我们首次报道了脑中存在NAADP的结合位点。与海胆卵匀浆不同,[³²P]NAADP可逆地结合于脑膜中的多个位点。不过,在这两个系统中,NAADP、2',3'-环NAADP和3'-NAADP在置换[³²P]NAADP时的效力顺序相同,且与它们从匀浆中动员钙离子的能力一致。这些数据表明,[³²P]NAADP可能与介导钙离子动员的受体结合。放射自显影显示,[³²P]NAADP结合位点在整个脑中的分布存在显著异质性。我们的数据有力地支持了NAADP诱导的钙离子信号在脑中发挥作用。

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