Koller Emily J, Chakrabarty Paramita
Department of Neuroscience, University of Florida, Gainesville, FL, United States.
Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, United States.
Front Mol Neurosci. 2020 Aug 21;13:151. doi: 10.3389/fnmol.2020.00151. eCollection 2020.
The inability of individual neurons to compensate for aging-related damage leads to a gradual loss of functional plasticity in the brain accompanied by progressive impairment in learning and memory. Whereas this loss in neuroplasticity is gradual during normal aging, in neurodegenerative diseases such as Alzheimer's disease (AD), this loss is accelerated dramatically, leading to the incapacitation of patients within a decade of onset of cognitive symptoms. The mechanisms that underlie this accelerated loss of neuroplasticity in AD are still not completely understood. While the progressively increasing proteinopathy burden, such as amyloid β (Aβ) plaques and tau tangles, definitely contribute directly to a neuron's functional demise, the role of non-neuronal cells in controlling neuroplasticity is slowly being recognized as another major factor. These non-neuronal cells include astrocytes, microglia, and oligodendrocytes, which through regulating brain homeostasis, structural stability, and trophic support, play a key role in maintaining normal functioning and resilience of the neuronal network. It is believed that chronic signaling from these cells affects the homeostatic network of neuronal and non-neuronal cells to an extent to destabilize this harmonious milieu in neurodegenerative diseases like AD. Here, we will examine the experimental evidence regarding the direct and indirect pathways through which astrocytes and microglia can alter brain plasticity in AD, specifically as they relate to the development and progression of tauopathy. In this review article, we describe the concepts of neuroplasticity and glial plasticity in healthy aging, delineate possible mechanisms underlying tau-induced plasticity dysfunction, and discuss current clinical trials as well as future disease-modifying approaches.
单个神经元无法代偿与衰老相关的损伤,导致大脑中功能可塑性逐渐丧失,同时学习和记忆能力不断受损。在正常衰老过程中,这种神经可塑性的丧失是渐进的,而在诸如阿尔茨海默病(AD)等神经退行性疾病中,这种丧失会急剧加速,导致患者在出现认知症状后的十年内丧失行动能力。AD中神经可塑性加速丧失的潜在机制仍未完全明确。虽然诸如淀粉样β(Aβ)斑块和tau缠结等蛋白质病变负担的逐渐增加肯定直接导致神经元功能死亡,但非神经元细胞在控制神经可塑性方面的作用正逐渐被视为另一个主要因素。这些非神经元细胞包括星形胶质细胞、小胶质细胞和少突胶质细胞,它们通过调节脑内稳态、结构稳定性和营养支持,在维持神经网络的正常功能和恢复力方面发挥关键作用。据信,这些细胞的慢性信号传导在一定程度上影响神经元和非神经元细胞的稳态网络,从而破坏像AD这样的神经退行性疾病中的这种和谐环境。在此处,我们将研究关于星形胶质细胞和小胶质细胞可通过直接和间接途径改变AD脑可塑性的实验证据,特别是它们与tau蛋白病的发生和发展的关系。在这篇综述文章中,我们描述了健康衰老过程中神经可塑性和胶质可塑性的概念,阐述了tau诱导的可塑性功能障碍的潜在机制,并讨论了当前的临床试验以及未来的疾病修饰方法。