Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield, Sheffield, UK.
Histol Histopathol. 2022 Mar;37(3):189-212. doi: 10.14670/HH-18-404. Epub 2021 Dec 9.
Adenosine deaminase (ADA) is a purine metabolism enzyme that catalyses the breakdown of adenosine and deoxyadenosine. The enzyme is important in several cellular processes, including the innate immune response and cellular differentiation, and it is also an important enzyme for the maintenance of brain homeostasis, in part due to its regulation of adenosine. Aberrant regulation of ADA enzyme activity has been linked to several neurodegenerative diseases and diseases that can result in neurological impairment. However, the mechanisms behind altered ADA regulation and how this leads to the development of neurological dysfunction are poorly characterised. This review summarises the current research on ADA and its role and regulation in disease pathology, with a focus on the central nervous system (CNS) and the neurodegenerative disease, amyotrophic lateral sclerosis (ALS).
腺苷脱氨酶(ADA)是一种嘌呤代谢酶,可催化腺苷和脱氧腺苷的分解。该酶在包括先天免疫反应和细胞分化在内的多个细胞过程中发挥着重要作用,它也是维持脑内稳态的重要酶,部分原因是其对腺苷的调节。ADA 酶活性的异常调节与几种神经退行性疾病和可能导致神经功能障碍的疾病有关。然而,改变的 ADA 调节的机制以及这如何导致神经功能障碍的发展仍未被充分描述。本综述总结了目前关于 ADA 及其在疾病发病机制中的作用和调节的研究,重点关注中枢神经系统(CNS)和神经退行性疾病肌萎缩侧索硬化症(ALS)。