Student Research Committee, Urmia University of Medical Sciences, Sero Road, Urmia, 5715799313, Iran.
Systematic Review and Meta-Analysis Expert Group (SRMEG), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Cell Commun Signal. 2023 Mar 14;21(1):60. doi: 10.1186/s12964-023-01072-w.
Alzheimer's disease (AD), the most common neurodegenerative disease worldwide, is caused by loss of neurons and synapses in central nervous system. Several causes for neuronal death in AD have been introduced, the most important of which are extracellular amyloid β (Aβ) accumulation and aggregated tau proteins. Increasing evidence suggest that targeting the process of Aβ production to reduce its deposition can serve as a therapeutic option for AD management. In this regard, therapeutic interventions shown that a disintegrin and metalloproteinase domain-containing protein (ADAM) 10, involved in non-amyloidogenic pathway of amyloid precursor protein processing, is known to be a suitable candidate. Therefore, this review aims to examine the molecular properties of ADAM10, its role in AD, and introduce it as a therapeutic target to reduce the progression of the disease. Video abstract.
阿尔茨海默病(AD)是全球最常见的神经退行性疾病,由中枢神经系统神经元和突触丧失引起。已经提出了 AD 中神经元死亡的几个原因,其中最重要的是细胞外淀粉样β(Aβ)积累和聚集的tau 蛋白。越来越多的证据表明,靶向 Aβ产生过程以减少其沉积可以作为 AD 管理的治疗选择。在这方面,治疗干预表明,参与淀粉样前体蛋白加工的非淀粉样途径的解整合素和金属蛋白酶域蛋白(ADAM)10 是一个合适的候选物。因此,本综述旨在研究 ADAM10 的分子特性、它在 AD 中的作用,并将其作为治疗靶点介绍以减缓疾病进展。视频摘要。