Eriksson Maria, Samuelsson Helena, Samuelsson Eva-Britt, Liu Leyuan, McKeehan Wallace L, Benedikz Eirikur, Sundström Erik
Karolinska Institutet, Department of Neurobiology, Care Sciences and Society, 141 86 Stockholm, Sweden.
Biochem Biophys Res Commun. 2007 Sep 14;361(1):127-32. doi: 10.1016/j.bbrc.2007.06.179. Epub 2007 Jul 16.
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.
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。