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神经元丰富的磷酸酶和肌动蛋白调节因子 3(Phactr3)/核骨架相关的 PP1 抑制蛋白(Scapinin)通过其蛋白磷酸酶 1 结合结构域调节树突形态。

Neuron-enriched phosphatase and actin regulator 3 (Phactr3)/ nuclear scaffold-associated PP1-inhibiting protein (Scapinin) regulates dendritic morphology via its protein phosphatase 1-binding domain.

机构信息

Laboratory of Molecular Neurobiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

Laboratory of Molecular Neurobiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan; Laboratory of Molecular Neurobiology, Faculty of Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

出版信息

Biochem Biophys Res Commun. 2020 Jul 23;528(2):322-329. doi: 10.1016/j.bbrc.2020.05.006. Epub 2020 May 15.

DOI:10.1016/j.bbrc.2020.05.006
PMID:32423795
Abstract

Phosphatase and actin regulator 3/nuclear scaffold-associated protein phosphatase 1-inhibiting protein (Phactr3/Scapinin) is an actin- and protein phosphatase 1 (PP1)-binding protein known to negatively regulate axon elongation. In this study, we examined the expression pattern of Phactr3/Scapinin in several tissues and investigated the effect of Phactr3/Scapinin on dendritic morphology of cortical neurons. Results showed that Phactr3/Scapinin expression was up-regulated in the developing brain and enriched in neurons and in the postsynaptic density fraction, but not in astrocytes. Overexpression of wild type or mutant Phactr3/Scapinin, which lacked actin-binding activity, resulted in increased dendritic complexity and percentage of spines with a mushroom or stubby shape, as well as a decrease in spine density. However, overexpression of mutant Phactr3/Scapinin that lacked PP1-binding activity did not. Taken together, these findings suggest that Phactr3/Scapinin expression is neuronal and might contribute to synaptic formation via distinct actin- and PP1-binding domains involved in dendritic and axonal morphology, respectively.

摘要

磷酸酶和肌动蛋白调节剂 3/核支架相关蛋白磷酸酶 1 抑制蛋白(Phactr3/Scapinin)是一种肌动蛋白和蛋白磷酸酶 1(PP1)结合蛋白,已知其可负向调节轴突伸长。在这项研究中,我们研究了 Phactr3/Scapinin 在几种组织中的表达模式,并研究了 Phactr3/Scapinin 对皮质神经元树突形态的影响。结果表明,Phactr3/Scapinin 在发育中的大脑中表达上调,富集在神经元和突触后密度部分,但不在星形胶质细胞中。野生型或缺乏肌动蛋白结合活性的突变型 Phactr3/Scapinin 的过表达导致树突复杂性增加和蘑菇形或短粗形棘突的比例增加,以及棘突密度降低。然而,缺乏 PP1 结合活性的突变型 Phactr3/Scapinin 的过表达则没有。总之,这些发现表明 Phactr3/Scapinin 的表达是神经元特有的,可能通过分别涉及树突和轴突形态的不同肌动蛋白和 PP1 结合结构域,有助于突触形成。

相似文献

1
Neuron-enriched phosphatase and actin regulator 3 (Phactr3)/ nuclear scaffold-associated PP1-inhibiting protein (Scapinin) regulates dendritic morphology via its protein phosphatase 1-binding domain.神经元丰富的磷酸酶和肌动蛋白调节因子 3(Phactr3)/核骨架相关的 PP1 抑制蛋白(Scapinin)通过其蛋白磷酸酶 1 结合结构域调节树突形态。
Biochem Biophys Res Commun. 2020 Jul 23;528(2):322-329. doi: 10.1016/j.bbrc.2020.05.006. Epub 2020 May 15.
2
Scapinin, the protein phosphatase 1 binding protein, enhances cell spreading and motility by interacting with the actin cytoskeleton.Scapinin,一种蛋白磷酸酶1结合蛋白,通过与肌动蛋白细胞骨架相互作用来增强细胞铺展和运动能力。
PLoS One. 2009;4(1):e4247. doi: 10.1371/journal.pone.0004247. Epub 2009 Jan 22.
3
Scapinin-induced inhibition of axon elongation is attenuated by phosphorylation and translocation to the cytoplasm.Scapinin 通过磷酸化和易位到细胞质来减弱轴突伸长的抑制作用。
J Biol Chem. 2011 Jun 3;286(22):19724-34. doi: 10.1074/jbc.M110.205781. Epub 2011 Apr 12.
4
Scapinin, a putative protein phosphatase-1 regulatory subunit associated with the nuclear nonchromatin structure.Scapinin,一种与核非染色质结构相关的假定蛋白磷酸酶-1调节亚基。
J Biol Chem. 2003 Nov 14;278(46):45611-9. doi: 10.1074/jbc.M305227200. Epub 2003 Aug 17.
5
Phactr3/scapinin, a member of protein phosphatase 1 and actin regulator (phactr) family, interacts with the plasma membrane via basic and hydrophobic residues in the N-terminus.Phactr3/鞘磷脂结合蛋白,蛋白磷酸酶1和肌动蛋白调节因子(Phactr)家族的成员,通过N端的碱性和疏水残基与质膜相互作用。
PLoS One. 2014 Nov 18;9(11):e113289. doi: 10.1371/journal.pone.0113289. eCollection 2014.
6
Genomic organization and expression pattern of scapinin (PHACTR3) in mouse and human.小鼠和人类中Scapinin(PHACTR3)的基因组结构与表达模式
Cytogenet Genome Res. 2006;115(1):23-9. doi: 10.1159/000094797.
7
Actin-associated neurabin-protein phosphatase-1 complex regulates hippocampal plasticity.肌动蛋白相关的神经结合蛋白-蛋白磷酸酶1复合物调节海马可塑性。
J Neurochem. 2006 Sep;98(6):1841-51. doi: 10.1111/j.1471-4159.2006.04070.x. Epub 2006 Aug 8.
8
Neurabin/protein phosphatase-1 complex regulates dendritic spine morphogenesis and maturation.神经素/蛋白磷酸酶-1复合物调节树突棘的形态发生和成熟。
Mol Biol Cell. 2005 May;16(5):2349-62. doi: 10.1091/mbc.e04-12-1054. Epub 2005 Mar 2.
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Differential regulation of AMPA receptor trafficking by neurabin-targeted synaptic protein phosphatase-1 in synaptic transmission and long-term depression in hippocampus.在海马体的突触传递和长时程抑制中,通过靶向神经肌动蛋白的突触蛋白磷酸酶-1对AMPA受体转运的差异性调控。
J Neurosci. 2007 Apr 25;27(17):4674-86. doi: 10.1523/JNEUROSCI.5365-06.2007.
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The actin-binding domain of spinophilin is necessary and sufficient for targeting to dendritic spines.亲嗜素的肌动蛋白结合结构域对于靶向树突棘而言是必要且充分的。
Neuromolecular Med. 2002;2(1):61-9. doi: 10.1385/NMM:2:1:61.

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