Shirai Remina, Cho Mizuka, Isogai Mikinori, Fukatsu Shoya, Okabe Miyu, Okawa Maho, Miyamoto Yuki, Torii Tomohiro, Yamauchi Junji
Laboratory of Molecular Neurology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Department of Pharmacology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.
Neurol Int. 2023 Aug 11;15(3):980-993. doi: 10.3390/neurolint15030063.
Frontotemporal dementia and/or amyotrophic lateral sclerosis type 7 (FTD/ALS7) is an autosomal dominant neurodegenerative disorder characterized by the onset of FTD and/or ALS, mainly in adulthood. Patients with some types of mutations, including the Thr104Asn (T104N) mutation of charged multivesicular body protein 2B (CHMP2B), have predominantly ALS phenotypes, whereas patients with other mutations have predominantly FTD phenotypes. A few mutations result in patients having both phenotypes approximately equally; however, the reason why phenotypes differ depending on the position of the mutation is unknown. CHMP2B comprises one part of the endosomal sorting complexes required for transport (ESCRT), specifically ESCRT-III, in the cytoplasm. We describe here, for the first time, that CHMP2B with the T104N mutation inhibits neuronal process elongation in the N1E-115 cell line, a model line undergoing neuronal differentiation. This inhibitory phenotype was accompanied by changes in marker protein expression. Of note, CHMP2B with the T104N mutation, but not the wild-type form, was preferentially accumulated in the Golgi body. Of the four major Golgi stress signaling pathways currently known, the pathway through Arf4, the small GTPase, was specifically upregulated in cells expressing CHMP2B with the T104N mutation. Conversely, knockdown of Arf4 with the cognate small interfering (si)RNA recovered the neuronal process elongation inhibited by the T104N mutation. These results suggest that the T104N mutation of CHMP2B inhibits morphological differentiation by triggering Golgi stress signaling, revealing a possible therapeutic molecular target for recovering potential molecular and cellular phenotypes underlying FTD/ALS7.
额颞叶痴呆和/或7型肌萎缩侧索硬化症(FTD/ALS7)是一种常染色体显性神经退行性疾病,其特征为FTD和/或ALS主要在成年期发病。某些类型突变的患者,包括带电多囊泡体蛋白2B(CHMP2B)的Thr104Asn(T104N)突变患者,主要表现为ALS表型,而其他突变患者主要表现为FTD表型。少数突变导致患者出现两种表型的比例大致相同;然而,表型因突变位置而异的原因尚不清楚。CHMP2B是细胞质中转运所需的内体分选复合物(ESCRT)的一部分,具体来说是ESCRT-III。我们首次在此描述,具有T104N突变的CHMP2B抑制N1E-115细胞系中的神经元突起伸长,N1E-115细胞系是一个正在进行神经元分化的模型细胞系。这种抑制表型伴随着标记蛋白表达的变化。值得注意的是,具有T104N突变的CHMP2B而非野生型形式优先积聚在高尔基体中。在目前已知的四条主要高尔基体应激信号通路中,通过小GTP酶Arf4的通路在表达具有T104N突变的CHMP2B的细胞中特异性上调。相反,用同源小干扰(si)RNA敲低Arf4可恢复受T104N突变抑制的神经元突起伸长。这些结果表明,CHMP2B的T104N突变通过触发高尔基体应激信号抑制形态分化,揭示了恢复FTD/ALS7潜在分子和细胞表型的一个可能的治疗分子靶点。