Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal - 576104, Karnataka, India.
Department of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal - 576104, Karnataka, India.
Ageing Res Rev. 2024 Dec;102:102566. doi: 10.1016/j.arr.2024.102566. Epub 2024 Oct 29.
Neurofilaments are intermediate filaments present in neurons. These provide structural support and maintain the size and shape of the neurons. Dysregulation, mutation, and aggregation of neurofilaments raise the levels of these proteins in the blood and cerebrospinal fluid (CSF), which are characteristic features of axonal damage and certain rare neurological diseases, such as Giant Axonal Neuropathy and Charcot-Mare-Tooth disease. Understanding the structure, dynamics, and function of neurofilaments has been greatly enhanced by a diverse range of biochemical and preclinical investigations conducted over more than four decades. Recently, there has been a resurgence of interest in post-translational modifications of neurofilaments, such as phosphorylation, aggregation, mutation, oxidation, etc. Over the past twenty years, several rare disorders have been studied from structural alterations of neurofilaments. These disorders are monitored by fluid biomarkers such as neurofilament light chains. Currently, there are many tools, such as Enzyme-Linked Immunosorbent Assay, Electrochemiluminescence Assay, Single-Molecule Array, Western/immunoblotting, etc., in use to assess the neurofilament proteins in Blood and CSF. However, all these techniques utilize expensive, non-specific, or antibody-based methods, which make them unsuitable for routine screening of neurodegenerative disorders. This provides room to search for newer sensitive, cost-effective, point-of-care tools for rapid screening of the disease. For a long time, the molecular mechanisms of neurofilaments have been poorly understood due to insufficient research attempts, and a deeper understanding of them remains elusive. Therefore, this review aims to highlight the available literature on molecular mechanisms of neurofilaments and the function of neurofilaments in axonal transport, axonal conduction, axonal growth, and neurofilament aggregation, respectively. Further, this review discusses the role of neurofilaments as potential biomarkers for the identification of several neurodegenerative diseases in clinical laboratory practice.
神经丝是存在于神经元中的中间丝。它们提供结构支持并维持神经元的大小和形状。神经丝的失调、突变和聚集会导致这些蛋白质在血液和脑脊液(CSF)中的水平升高,这是轴突损伤和某些罕见神经疾病的特征,如巨轴索神经病和夏科-马里-图病。通过四十多年来进行的各种生化和临床前研究,对神经丝的结构、动态和功能有了更深入的了解。最近,人们对神经丝的翻译后修饰(如磷酸化、聚集、突变、氧化等)重新产生了兴趣。在过去的二十年中,已经从神经丝的结构改变研究了几种罕见疾病。这些疾病通过神经丝轻链等体液生物标志物进行监测。目前,有许多工具,如酶联免疫吸附试验、电化学发光测定、单分子阵列、Western/免疫印迹等,用于评估血液和脑脊液中的神经丝蛋白。然而,所有这些技术都使用昂贵、非特异性或基于抗体的方法,这使得它们不适合常规筛查神经退行性疾病。这为寻找新的、更敏感、更具成本效益的即时护理工具来快速筛查疾病提供了空间。由于研究尝试不足,神经丝的分子机制长期以来一直知之甚少,对其的深入了解仍然难以捉摸。因此,本综述旨在重点介绍神经丝的分子机制以及神经丝在轴突运输、轴突传导、轴突生长和神经丝聚集中的功能的现有文献。此外,本综述还讨论了神经丝作为几种神经退行性疾病在临床实验室实践中识别的潜在生物标志物的作用。