Khan Aiza, Sergi Consolato M
Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada.
Division of Anatomic Pathology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada.
Front Pharmacol. 2022 Jun 29;13:902259. doi: 10.3389/fphar.2022.902259. eCollection 2022.
Neuraminidase 1 (NEU1) is considered to be the most abundant and ubiquitous mammalian enzyme, with a broad tissue distribution. It plays a crucial role in a variety of cellular mechanisms. The deficiency of NEU1 has been implicated in various pathological manifestations of sialidosis and neurodegeneration. Thus, it is a novel therapeutic target for neurodegenerative changes in the Alzheimer's brain. However, to manipulate NEU1 as a therapeutic target, it is imperative to understand that, although NEU1 is commonly known for its lysosomal catabolic function, it is also involved in other pathways. NEU1 is involved in immune response modulation, elastic fiber assembly modulation, insulin signaling, and cell proliferation. In recent years, our knowledge of NEU1 has continued to grow, yet, at the present moment, current data is still limited. In addition, the unique biochemical properties of NEU1 make it challenging to target it as an effective therapeutic option for sialidosis, which is a rare disease but has an enormous patient burden. However, the fact that NEU1 has been linked to the pathology of Alzheimer's disease, which is rapidly growing worldwide, makes it more relevant to be studied and explored. In the present study, the authors have discussed various cellular mechanisms involving NEU1 and how they are relevant to sialidosis and Alzheimer's disease.
神经氨酸酶1(NEU1)被认为是哺乳动物中含量最丰富且分布最广泛的酶,具有广泛的组织分布。它在多种细胞机制中发挥着关键作用。NEU1的缺乏与涎酸贮积症和神经退行性变的各种病理表现有关。因此,它是阿尔茨海默病大脑神经退行性变化的一个新的治疗靶点。然而,要将NEU1作为治疗靶点进行操控,必须明白,尽管NEU1通常以其溶酶体分解代谢功能而闻名,但它也参与其他途径。NEU1参与免疫反应调节、弹性纤维组装调节、胰岛素信号传导和细胞增殖。近年来,我们对NEU1的认识不断增加,但目前,现有数据仍然有限。此外,NEU1独特的生化特性使其难以成为涎酸贮积症(一种罕见但患者负担巨大的疾病)的有效治疗选择。然而,NEU1与阿尔茨海默病的病理相关,而阿尔茨海默病在全球范围内正在迅速增加,这使得对其进行研究和探索更具意义。在本研究中,作者讨论了涉及NEU1的各种细胞机制以及它们与涎酸贮积症和阿尔茨海默病的相关性。