| Literature DB >> 32423795 |
Tomoaki Miyata1, Keietsu Kikuchi1, Daisuke Ihara2, Maki Kaito1, Yuta Ishibashi1, Tomoyuki Hakamata1, Tetsuya Yamada1, Mitsuru Ishikawa3, Miho Mizukoshi1, Shizuku Shoji1, Mamoru Fukuchi4, Masaaki Tsuda1, Yamato Hida5, Toshihisa Ohtsuka5, Marisa Kaneda1, Akiko Tabuchi6.
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.Entities:
Keywords: Actin; Dendrite; Dendritic spine; Nuclear scaffold-associated PP1-Inhibiting protein; Phosphatase and actin regulator; Protein phosphatase
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Year: 2020 PMID: 32423795 DOI: 10.1016/j.bbrc.2020.05.006
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575