Yokoi Fumiaki, Tanaka Yuuna, Sakai Akari, Isogai Nao, Miyata Shiori, Mitsui Shinichi
Department of Rehabilitation Sciences, Gunma University Graduate School of Health Sciences, 3-39-22, Showa-Machi, Maebashi, Gunma, 371-8514, Japan.
Department of Occupational Therapy, School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Geroscience. 2025 May 23. doi: 10.1007/s11357-025-01694-7.
Truncating mutation in motopsin (neurotrypsin/PRSS12) gene causes an autosomal recessive non-syndromic intellectual disability. Since motopsin cleaves agrin, motopsin deficiency causes accumulation of long form agrin. Agrin binds amyloid β (Aβ) and accelerates Aβ fibril formation in Alzheimer's disease (AD). Down's syndrome (DS) exhibits AD-like neuropathological changes. Agrin also contributes to Parkinson's disease (PD). Degeneration of cholinergic neurons is relevant to AD, whereas degeneration of dopaminergic neurons causes PD and PD-associated cognitive impairment and dementia. Although there is a functional relationship between agrin and amyloidosis, it has not been clear whether motopsin deficiency induces amyloid neuropathy or not. Here, motopsin knock-out (KO) mice increased hippocampal amyloid and phosphorylated tau deposits. Agrin and amyloid oligomers were colocalized in the amyloid angiopathy. Motopsin KO mice also exhibited motor deficits. Motopsin KO male mice decreased cholinergic neurons in the vertical limb of the diagonal band of Broca and dopaminergic neurons in the substantia nigra compacta and the ventral tegmental area, and showed long-term memory deficits for object recognition, hypoactivity, and shorter sleeping time. Motopsin KO female mice decreased cholinergic neurons in the medial septum and showed hyperactivity. The results suggest that this intellectual disability is produced by a complex mechanism relating to AD, DS, PD, PD-associated cognitive impairment, and cerebrovascular dementia. The results also suggest that motopsin KO mouse can be a novel animal model for these diseases. Development of therapeutics, that reduce amyloid and phosphorylated tau deposits and protect cholinergic and dopaminergic neurons, will be useful to prevent the progress of this disease.
视动蛋白(神经胰蛋白酶/PRSS12)基因的截短突变会导致常染色体隐性非综合征性智力障碍。由于视动蛋白可切割聚集蛋白聚糖,视动蛋白缺乏会导致长型聚集蛋白聚糖积累。聚集蛋白聚糖与淀粉样β蛋白(Aβ)结合,并加速阿尔茨海默病(AD)中Aβ纤维的形成。唐氏综合征(DS)表现出类似AD的神经病理变化。聚集蛋白聚糖也与帕金森病(PD)有关。胆碱能神经元的退化与AD相关,而多巴胺能神经元的退化会导致PD以及与PD相关的认知障碍和痴呆。尽管聚集蛋白聚糖与淀粉样变性之间存在功能关系,但视动蛋白缺乏是否会诱发淀粉样神经病变尚不清楚。在此,视动蛋白基因敲除(KO)小鼠的海马淀粉样蛋白和磷酸化tau蛋白沉积增加。聚集蛋白聚糖和淀粉样寡聚体在淀粉样血管病中共定位。视动蛋白KO小鼠还表现出运动缺陷。视动蛋白KO雄性小鼠在布罗卡斜角带垂直支中的胆碱能神经元以及黑质致密部和腹侧被盖区中的多巴胺能神经元减少,并表现出物体识别的长期记忆缺陷、活动减退和睡眠时间缩短。视动蛋白KO雌性小鼠在内侧隔区的胆碱能神经元减少,并表现出活动亢进。结果表明,这种智力障碍是由与AD、DS、PD、PD相关的认知障碍和脑血管性痴呆相关的复杂机制产生的。结果还表明,视动蛋白KO小鼠可以成为这些疾病的新型动物模型。开发能够减少淀粉样蛋白和磷酸化tau蛋白沉积并保护胆碱能和多巴胺能神经元的治疗方法,将有助于预防这种疾病的进展。