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N-甲基-D-天冬氨酸受体亚基NR3A在大脑中与微管相关蛋白1S相互作用。

The NMDAR subunit NR3A interacts with microtubule-associated protein 1S in the brain.

作者信息

Eriksson Maria, Samuelsson Helena, Samuelsson Eva-Britt, Liu Leyuan, McKeehan Wallace L, Benedikz Eirikur, Sundström Erik

机构信息

Karolinska Institutet, Department of Neurobiology, Care Sciences and Society, 141 86 Stockholm, Sweden.

出版信息

Biochem Biophys Res Commun. 2007 Sep 14;361(1):127-32. doi: 10.1016/j.bbrc.2007.06.179. Epub 2007 Jul 16.

Abstract

When screening a brain cDNA library, we found that the N-methyl-D-aspartate receptor subunit NR3A binds to microtubule-associated protein (MAP) 1S/chromosome 19 open reading frame 5 (C19ORF5). The interaction was confirmed in vitro and in vivo, and binding of MAP1S was localized to the membrane-proximal part of the NR3A C-terminus. MAP1S belongs to the same family as MAP1A and MAP1B, and was found to be abundant in both postnatal and adult rat brain. In hippocampal neurons the distribution-pattern of MAP1S resembled that of beta-tubulin III, but a fraction of the protein colocalized with synaptic markers synapsin and postsynaptic density protein 95 (PSD95), in beta-tubulin III-negative filopodia-like protrusions. There was coexistance between MAP1S and NR3A immunoreactivity in neurite shafts and occasionally in filopodia-like processes. MAP1S potentially links NR3A to the cytoskeleton, and may stabilize NR3A-containing receptors at the synapse and regulate their movement between synaptic and extrasynaptic sites.

摘要

在筛选脑cDNA文库时,我们发现N-甲基-D-天冬氨酸受体亚基NR3A与微管相关蛋白(MAP)1S/19号染色体开放阅读框5(C19ORF5)结合。这种相互作用在体外和体内均得到证实,且MAP1S的结合定位于NR3A C末端的膜近端部分。MAP1S与MAP1A和MAP1B属于同一家族,且在新生和成年大鼠脑中均大量存在。在海马神经元中,MAP1S的分布模式类似于β-微管蛋白III,但在β-微管蛋白III阴性的丝状伪足样突起中,有一部分该蛋白与突触标记物突触素和突触后致密蛋白95(PSD95)共定位。在神经突轴中,偶尔在丝状伪足样突起中,MAP1S和NR3A免疫反应性共存。MAP1S可能将NR3A与细胞骨架联系起来,并可能在突触处稳定含NR3A的受体,并调节它们在突触和突触外位点之间的移动。

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