Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Fuku-ura 3-9, Kanazawa Ward, Yokohama 236-0004, Japan.
Biochem Biophys Res Commun. 2012 Feb 10;418(2):390-5. doi: 10.1016/j.bbrc.2012.01.033. Epub 2012 Jan 18.
Myelin-derived axon growth inhibitors, such as Nogo, bind to Nogo receptor-1 (NgR1) and thereby limit the action of axonal regeneration after injury in the adult central nervous system. Recently, we have found that cartilage acidic protein-1B (Crtac1B)/lateral olfactory tract usher substance (LOTUS) binds to NgR1 and functions as an endogenous NgR1 antagonist. To examine the functional domain of LOTUS in the antagonism to NgR1, analysis using the deletion mutants of LOTUS was performed and revealed that the carboxyl-terminal region (UA/EC domain) of LOTUS bound to NgR1. The UA/EC fragment of LOTUS overexpressed together with NgR1 in COS7 cells abolished the binding of Nogo66 to NgR1. Overexpression of the UA/EC fragment in cultured chick dorsal root ganglion neurons suppressed Nogo66-induced growth cone collapse. These findings suggest that the UA/EC region is a functional domain of LOTUS serving for an antagonistic action to NgR1.
髓鞘来源的轴突生长抑制剂,如 Nogo,与 Nogo 受体-1(NgR1)结合,从而限制成年中枢神经系统损伤后的轴突再生作用。最近,我们发现软骨酸性蛋白-1B(Crtac1B)/外侧嗅束引导物质(LOTUS)与 NgR1 结合,并作为内源性 NgR1 拮抗剂发挥作用。为了研究 LOTUS 在拮抗 NgR1 中的功能域,对 LOTUS 的缺失突变体进行了分析,结果表明 LOTUS 的羧基末端区域(UA/EC 结构域)与 NgR1 结合。在 COS7 细胞中与 NgR1 共表达 LOTUS 的 UA/EC 片段可消除 Nogo66 与 NgR1 的结合。在培养的鸡背根神经节神经元中过表达 UA/EC 片段可抑制 Nogo66 诱导的生长锥塌陷。这些发现表明 UA/EC 区域是 LOTUS 的一个功能域,可拮抗 NgR1。