Molecular Medical Bioscience Laboratory, Department of Medical Life Science, Yokohama City University Graduate School of Medical Life Science, Yokohama 230-0045, Japan.
Department of Anatomy & Developmental Biology, Faculty of Medicine, Shimane University, Izumo 693-8501, Japan.
Cells. 2024 Aug 17;13(16):1369. doi: 10.3390/cells13161369.
Neurite outgrowth is a crucial process for organizing neuronal circuits in neuronal development and regeneration after injury. Regenerative failure in the adult mammalian central nervous system (CNS) is attributed to axonal growth inhibitors such as the Nogo protein that commonly binds to Nogo receptor-1 (NgR1). We previously reported that lateral olfactory tract usher substance (LOTUS) functions as an endogenous antagonist for NgR1 in forming neuronal circuits in the developing brain and improving axonal regeneration in the adult injured CNS. However, another molecular and cellular function of LOTUS remains unknown. In this study, we found that cultured retinal explant neurons extend their neurites on the LOTUS-coating substrate. This action was also observed in cultured retinal explant neurons derived from -deficient mouse embryos, indicating that the promoting action of LOTUS on neurite outgrowth may be mediated by unidentified LOTUS-binding protein(s). We therefore screened the binding partner(s) of LOTUS by using a liquid chromatography-tandem mass spectrometry (LC-MS/MS). LC-MS/MS analysis and pull-down assay showed that LOTUS interacts with Teneurin-4 (Ten-4), a cell adhesion molecule. RNAi knockdown of inhibited neurite outgrowth on the LOTUS substrate in retinoic acid (RA)-treated Neuro2A cells. Furthermore, a soluble form of Ten-4 attenuates the promoting action on neurite outgrowth in cultured retinal explant neurons on the LOTUS substrate. These results suggest that LOTUS promotes neurite outgrowth by interacting with Ten-4. Our findings may provide a new molecular mechanism of LOTUS to contribute to neuronal circuit formation in development and to enhance axonal regeneration after CNS injury.
神经突生长是神经元发育和损伤后再生过程中组织神经元回路的关键过程。成年哺乳动物中枢神经系统 (CNS) 的再生失败归因于轴突生长抑制剂,如普遍与 NgR1 结合的 Nogo 蛋白。我们之前报道过,外侧嗅束引导物质 (LOTUS) 在形成发育中大脑中的神经元回路和改善成年损伤 CNS 中的轴突再生方面,作为 NgR1 的内源性拮抗剂发挥作用。然而,LOTUS 的另一个分子和细胞功能仍然未知。在这项研究中,我们发现培养的视网膜外植体神经元在 LOTUS 涂层基质上延伸其神经突。在源自 -缺陷小鼠胚胎的培养的视网膜外植体神经元中也观察到了这种作用,表明 LOTUS 对神经突生长的促进作用可能是由未鉴定的 LOTUS 结合蛋白 (s) 介导的。因此,我们通过使用液相色谱-串联质谱 (LC-MS/MS) 筛选 LOTUS 的结合伴侣 (s)。LC-MS/MS 分析和下拉测定表明,LOTUS 与细胞粘附分子 Teneurin-4 (Ten-4) 相互作用。在 RA 处理的 Neuro2A 细胞中,RNAi 敲低 抑制了 LOTUS 基质上的神经突生长。此外,Ten-4 的可溶性形式减弱了 LOTUS 基质上培养的视网膜外植体神经元中对神经突生长的促进作用。这些结果表明,LOTUS 通过与 Ten-4 相互作用促进神经突生长。我们的发现可能为 LOTUS 提供了一个新的分子机制,有助于发育中的神经元回路形成,并增强 CNS 损伤后的轴突再生。