Department of Pharmacy, BRAC University, Dhaka 1212, Bangladesh.
Biomolecules. 2018 Sep 10;8(3):93. doi: 10.3390/biom8030093.
Even though Alzheimer's disease (AD) is of significant interest to the scientific community, its pathogenesis is very complicated and not well-understood. A great deal of progress has been made in AD research recently and with the advent of these new insights more therapeutic benefits may be identified that could help patients around the world. Much of the research in AD thus far has been very neuron-oriented; however, recent studies suggest that glial cells, i.e., microglia, astrocytes, oligodendrocytes, and oligodendrocyte progenitor cells (NG2 glia), are linked to the pathogenesis of AD and may offer several potential therapeutic targets against AD. In addition to a number of other functions, glial cells are responsible for maintaining homeostasis (i.e., concentration of ions, neurotransmitters, etc.) within the central nervous system (CNS) and are crucial to the structural integrity of neurons. This review explores the: (i) role of glial cells in AD pathogenesis; (ii) complex functionalities of the components involved; and (iii) potential therapeutic targets that could eventually lead to a better quality of life for AD patients.
尽管阿尔茨海默病(AD)是科学界非常关注的问题,但它的发病机制非常复杂,尚未得到很好的理解。最近在 AD 研究方面取得了很大进展,随着这些新见解的出现,可能会发现更多的治疗益处,从而帮助世界各地的患者。迄今为止,AD 的大部分研究都非常侧重于神经元;然而,最近的研究表明,神经胶质细胞(即小胶质细胞、星形胶质细胞、少突胶质细胞和少突胶质细胞前体细胞(NG2 胶质细胞))与 AD 的发病机制有关,并可能为 AD 提供几个潜在的治疗靶点。除了许多其他功能外,神经胶质细胞还负责维持中枢神经系统(CNS)内的内环境稳定(即离子、神经递质等的浓度),对于神经元的结构完整性至关重要。本综述探讨了:(i)神经胶质细胞在 AD 发病机制中的作用;(ii)涉及的成分的复杂功能;以及(iii)最终可能为 AD 患者带来更高生活质量的潜在治疗靶点。