Kawamoto Yuko, Tada Mikiko, Asano Tetsuya, Nakamura Haruko, Jitsuki-Takahashi Aoi, Makihara Hiroko, Kubota Shun, Hashiguchi Shunta, Kunii Misako, Ohshima Toshio, Goshima Yoshio, Takeuchi Hideyuki, Doi Hiroshi, Nakamura Fumio, Tanaka Fumiaki
Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Front Neurol. 2022 Sep 27;13:994676. doi: 10.3389/fneur.2022.994676. eCollection 2022.
In amyotrophic lateral sclerosis (ALS), neurodegeneration is characterized by distal axonopathy that begins at the distal axons, including the neuromuscular junctions, and progresses proximally in a "dying back" manner prior to the degeneration of cell bodies. However, the molecular mechanism for distal axonopathy in ALS has not been fully addressed. Semaphorin 3A (Sema3A), a repulsive axon guidance molecule that phosphorylates collapsin response mediator proteins (CRMPs), is known to be highly expressed in Schwann cells near distal axons in a mouse model of ALS. To clarify the involvement of Sema3A-CRMP signaling in the axonal pathogenesis of ALS, we investigated the expression of phosphorylated CRMP1 (pCRMP1) in the spinal cords of 35 patients with sporadic ALS and seven disease controls. In ALS patients, we found that pCRMP1 accumulated in the proximal axons and co-localized with phosphorylated neurofilaments (pNFs), which are a major protein constituent of spheroids. Interestingly, the pCRMP1:pNF ratio of the fluorescence signal in spheroid immunostaining was inversely correlated with disease duration in 18 evaluable ALS patients, indicating that the accumulation of pCRMP1 may precede that of pNFs in spheroids or promote ALS progression. In addition, overexpression of a phospho-mimicking CRMP1 mutant inhibited axonal outgrowth in Neuro2A cells. Taken together, these results indicate that pCRMP1 may be involved in the pathogenesis of axonopathy in ALS, leading to spheroid formation through the proximal progression of axonopathy.
在肌萎缩侧索硬化症(ALS)中,神经退行性变的特征是远端轴突病,其始于包括神经肌肉接头在内的远端轴突,并在细胞体变性之前以“回退”方式向近端进展。然而,ALS中远端轴突病的分子机制尚未得到充分阐明。信号素3A(Sema3A)是一种可使塌陷反应介导蛋白(CRMPs)磷酸化的排斥性轴突导向分子,已知在ALS小鼠模型中,其在远端轴突附近的施万细胞中高度表达。为了阐明Sema3A-CRMP信号在ALS轴突发病机制中的作用,我们研究了35例散发性ALS患者和7例疾病对照者脊髓中磷酸化CRMP1(pCRMP1)的表达。在ALS患者中,我们发现pCRMP1在近端轴突中积累,并与磷酸化神经丝(pNFs)共定位,pNFs是球体的主要蛋白质成分。有趣的是,在18例可评估的ALS患者中,球体免疫染色中荧光信号的pCRMP1:pNF比值与疾病持续时间呈负相关,这表明pCRMP1在球体中的积累可能先于pNFs,或促进ALS进展。此外,磷酸化模拟CRMP1突变体的过表达抑制了Neuro2A细胞中的轴突生长。综上所述,这些结果表明pCRMP1可能参与了ALS轴突病的发病机制,通过轴突病的近端进展导致球体形成。