Common cytokine receptor gamma chain family cytokines activate MAPK, PI3K, and JAK/STAT pathways in microglia to influence Alzheimer’s Disease

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Hannah Zuppe, Erin Reed
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引用次数: 0

Abstract

Dementia is an umbrella term used to describe deterioration of cognitive function. It is the seventh leading cause of death and is one of the major causes of dependence among older people globally. Alzheimer’s Disease (AD) contributes to approximately 60–70% of dementia cases and is characterized by the accumulation of amyloid plaques and tau tangles in the brain. Neuroinflammation is now widely accepted as another disease hallmark, playing a role in both the response to and the perpetuation of disease processes. Microglia are brain-resident immune cells that are initially effective at clearing amyloid plaques but contribute to the damaging inflammatory milieu of the brain as disease progresses. Circulating peripheral immune cells contribute to this inflammatory environment through cytokine secretion, creating a positive feedback loop with the microglia. One group of these peripherally derived cytokines acting on microglia is the common cytokine receptor γ chain family. These cytokines bind heterodimer receptors to activate three major signaling pathways: MAPK, PI3K, and JAK/STAT. This perspective will look at the mechanisms of these three pathways in microglia and highlight the future directions of this research and potential therapeutics.
常见细胞因子受体γ链家族细胞因子激活小胶质细胞中的 MAPK、PI3K 和 JAK/STAT 通路,从而影响阿尔茨海默病的病情
痴呆症是描述认知功能退化的总称。它是全球第七大死亡原因,也是导致老年人依赖他人的主要原因之一。阿尔茨海默病(AD)约占痴呆症病例的 60-70%,其特征是淀粉样蛋白斑块和 tau 结在大脑中的积累。神经炎症现已被广泛认为是另一种疾病特征,在疾病的反应和持续过程中都发挥着作用。小胶质细胞是驻留在大脑中的免疫细胞,最初能有效清除淀粉样蛋白斑块,但随着疾病的发展,它们会加剧大脑中的破坏性炎症环境。循环中的外周免疫细胞通过分泌细胞因子促进这种炎症环境,与小胶质细胞形成正反馈循环。这些作用于小胶质细胞的外周衍生细胞因子中有一类是常见的细胞因子受体γ链家族。这些细胞因子与异源二聚体受体结合,激活三种主要信号通路:MAPK、PI3K 和 JAK/STAT。本视角将探讨这三种途径在小胶质细胞中的作用机制,并重点介绍这一研究的未来方向和潜在疗法。
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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