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小胶质细胞代谢重编程:神经退行性疾病的新见解和治疗策略。

Microglial Metabolic Reprogramming: Emerging Insights and Therapeutic Strategies in Neurodegenerative Diseases.

机构信息

Shenzhen Bao'an Traditional Chinese Medicine Hospital, Shenzhen, China.

School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, China.

出版信息

Cell Mol Neurobiol. 2023 Oct;43(7):3191-3210. doi: 10.1007/s10571-023-01376-y. Epub 2023 Jun 21.

Abstract

Microglia, the resident immune cells of the central nervous system, play a critical role in maintaining brain homeostasis. However, in neurodegenerative conditions, microglial cells undergo metabolic reprogramming in response to pathological stimuli, including Aβ plaques, Tau tangles, and α-synuclein aggregates. This metabolic shift is characterized by a transition from oxidative phosphorylation (OXPHOS) to glycolysis, increased glucose uptake, enhanced production of lactate, lipids, and succinate, and upregulation of glycolytic enzymes. These metabolic adaptations result in altered microglial functions, such as amplified inflammatory responses and diminished phagocytic capacity, which exacerbate neurodegeneration. This review highlights recent advances in understanding the molecular mechanisms underlying microglial metabolic reprogramming in neurodegenerative diseases and discusses potential therapeutic strategies targeting microglial metabolism to mitigate neuroinflammation and promote brain health. Microglial Metabolic Reprogramming in Neurodegenerative Diseases This graphical abstract illustrates the metabolic shift in microglial cells in response to pathological stimuli and highlights potential therapeutic strategies targeting microglial metabolism for improved brain health.

摘要

小胶质细胞是中枢神经系统的固有免疫细胞,在维持脑内环境稳定方面发挥着关键作用。然而,在神经退行性疾病中,小胶质细胞会对包括 Aβ 斑块、Tau 缠结和α-突触核蛋白聚集在内的病理刺激发生代谢重编程。这种代谢转变的特征是从氧化磷酸化 (OXPHOS) 向糖酵解转变,葡萄糖摄取增加,乳酸、脂质和琥珀酸的生成增强,糖酵解酶的表达上调。这些代谢适应性导致小胶质细胞功能发生改变,例如炎症反应放大和吞噬能力减弱,从而加剧神经退行性变。这篇综述强调了理解神经退行性疾病中小胶质细胞代谢重编程的分子机制的最新进展,并讨论了针对小胶质细胞代谢的潜在治疗策略,以减轻神经炎症并促进大脑健康。

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