Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Wicking Dementia Research and Education Centre, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Neurobiol Aging. 2021 Sep;105:340-348. doi: 10.1016/j.neurobiolaging.2021.03.010. Epub 2021 Mar 27.
Tauopathies are a group of neurodegenerative diseases that involve pathological changes to the tau protein. Neuroinflammation is a commonly reported feature of tauopathies that has been demonstrated to exacerbate tau pathology and, hence, neurodegeneration. Microglia can mediate the inflammatory response in order to maintain brain homeostasis. In the aged brain, microglia are reported to undergo morphological and functional changes, adopting a pro-inflammatory profile and loss of homeostatic functions. Dystrophic and dysfunctional microglia are associated with tau pathology in the healthy and diseased brain which is proposed to contribute to disease development and progression. Microglia have also been recently demonstrated to possess sexually dimorphic roles in the developing, adult and aged brain. The sex differences in microglial functionality suggest that microglia may contribute to tauopathies which may differ between sexes. This review highlights the detrimental loop between age-related microglial changes and tau pathology with implications for microglial sexual dichotomy.
tau 病是一组涉及 tau 蛋白病理性改变的神经退行性疾病。神经炎症是 tau 病的一个常见特征,已被证明会加剧 tau 病理和神经退行性变。小胶质细胞可以介导炎症反应,以维持大脑内环境平衡。在衰老的大脑中,小胶质细胞被报道会发生形态和功能上的改变,表现出促炎表型和失去内稳态功能。在健康和患病的大脑中,与 tau 病理相关的是功能障碍和功能障碍的小胶质细胞,这被认为有助于疾病的发展和进展。最近还发现小胶质细胞在发育、成年和衰老的大脑中具有性别二态性作用。小胶质细胞功能的性别差异表明,小胶质细胞可能会导致 tau 病,而 tau 病在不同性别之间可能存在差异。这篇综述强调了与年龄相关的小胶质细胞变化和 tau 病理之间的恶性循环,这对小胶质细胞的性别二态性有影响。