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