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蛋白激酶A介导的α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体磷酸化的新型阻断作用

Novel blockade of protein kinase A-mediated phosphorylation of AMPA receptors.

作者信息

Vanhoose Amanda M, Clements Julie M, Winder Danny G

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0615, USA.

出版信息

J Neurosci. 2006 Jan 25;26(4):1138-45. doi: 10.1523/JNEUROSCI.3572-05.2006.

Abstract

The phosphorylation state of the glutamate receptor subtype 1 (GluR1) subunit of the AMPA receptor (AMPAR) plays a critical role in synaptic expression of the receptor, channel properties, and synaptic plasticity. Several Gs-coupled receptors that couple to protein kinase A (PKA) readily recruit phosphorylation of GluR1 at S845. Conversely, activation of the ionotropic glutamate NMDA receptor (NMDAR) readily recruits dephosphorylation of the same GluR1 site through Ca2+-mediated recruitment of phosphatase activity. In a physiological setting, receptor activation often overlaps and crosstalk between coactivation of multiple signaling cascades can result in differential regulation of a given substrate. After investigating the effect of coactivation of the NMDAR and the Gs-coupled beta-adrenergic receptor on GluR1 phosphorylation state, we have observed a novel signal that prevents PKA-mediated phosphorylation of GluR1 at serine site 845. This blockade of GluR1 phosphorylation is dependent on cellular depolarization recruited by either NMDAR or AMPAR activation, independent of Ca2+ and independent of calcineurin, protein phosphatase 1, and/or protein phosphatase 2A activity. Thus, in addition to the typical kinase-phosphatase rivalry mediating protein phosphorylation state, we have identified a novel form of phospho-protein regulation that occurs at GluR1 and may also occur at several other PKA substrates.

摘要

α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)的谷氨酸受体亚型1(GluR1)亚基的磷酸化状态在该受体的突触表达、通道特性及突触可塑性中起着关键作用。几种与G蛋白偶联且与蛋白激酶A(PKA)偶联的受体能轻易促使GluR1在S845位点发生磷酸化。相反,离子型谷氨酸N-甲基-D-天冬氨酸受体(NMDAR)的激活能通过Ca2+介导的磷酸酶活性募集轻易促使同一GluR1位点发生去磷酸化。在生理环境中,受体激活常常重叠,多个信号级联的共同激活之间的串扰可导致对给定底物的差异调节。在研究NMDAR和与G蛋白偶联的β-肾上腺素能受体共同激活对GluR1磷酸化状态的影响后,我们观察到一种新信号,它可阻止PKA介导的GluR1在丝氨酸845位点的磷酸化。这种对GluR1磷酸化的阻断依赖于由NMDAR或AMPAR激活引发的细胞去极化,与Ca2+无关,也与钙调神经磷酸酶、蛋白磷酸酶1和/或蛋白磷酸酶2A的活性无关。因此,除了介导蛋白质磷酸化状态的典型激酶 - 磷酸酶竞争外,我们还发现了一种在GluR1发生的新型磷酸化蛋白调节形式,并且可能也发生在其他几种PKA底物上。

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