Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10065, USA.
J Neurochem. 2010 Jul;114(1):182-90. doi: 10.1111/j.1471-4159.2010.06743.x. Epub 2010 Apr 9.
The Wiskott-Aldrich syndrome protein (WASP)-family verprolin homologous protein 1 (WAVE1) is a key regulator of Arp (actin-related protein) 2/3 complex-mediated actin polymerization. We have established previously that the state of phosphorylation of WAVE1 at three distinct residues controls its ability to regulate actin polymerization and spine morphology. Cyclin-dependent kinase 5 phosphorylates WAVE1 at Ser310, Ser397 and Ser441 to a high basal stoichiometry, resulting in inhibition of WAVE1 activity. Our previous and current studies show that WAVE1 can be dephosphorylated at all three sites and thereby activated upon stimulation of the D1 subclass of dopamine receptors and of the NMDA subclass of glutamate receptors, acting through cAMP and Ca(2+) signaling pathways, respectively. Specifically, we have identified protein phosphatase-2A and protein phosphatase-2B as the effectors for these second messengers. These phosphatases act on different sites to mediate receptor-induced signaling pathways, which would lead to activation of WAVE1.
Wiskott-Aldrich 综合征蛋白 (WASP)-家族丝氨酸/苏氨酸蛋白激酶同源物 1(WAVE1)是 Arp(肌动蛋白相关蛋白)2/3 复合物介导的肌动蛋白聚合的关键调节因子。我们之前已经证实,WAVE1 在三个不同残基的磷酸化状态控制其调节肌动蛋白聚合和脊柱形态的能力。细胞周期蛋白依赖性激酶 5 在 Ser310、Ser397 和 Ser441 处将 WAVE1 磷酸化至高基础比例,从而抑制 WAVE1 活性。我们之前和目前的研究表明,WAVE1 可以在所有三个位点去磷酸化,从而在 D1 类多巴胺受体和 NMDA 类谷氨酸受体的刺激下被激活,分别通过 cAMP 和 Ca(2+)信号通路。具体而言,我们已经确定蛋白磷酸酶-2A 和蛋白磷酸酶-2B 是这些第二信使的效应物。这些磷酸酶在不同的位点起作用,介导受体诱导的信号通路,从而导致 WAVE1 的激活。