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网络化大脑中神经炎症的双重性质。

The dual nature of neuroinflammation in networked brain.

作者信息

Müller Ludmila, Di Benedetto Svetlana, Müller Viktor

机构信息

Max Planck Institute for Human Development, Center for Lifespan Psychology, Berlin, Germany.

出版信息

Front Immunol. 2025 Aug 20;16:1659947. doi: 10.3389/fimmu.2025.1659947. eCollection 2025.

Abstract

Neuroinflammation is a dynamic, context-sensitive process that plays essential roles in brain development, maintenance, and response to injury. It reflects a finely balanced neuroimmune state-facilitating repair and adaptation under homeostatic conditions, while also contributing to dysfunction when dysregulated or chronically activated. In this mini-review, we examine the cellular and molecular mechanisms underlying neuroinflammatory responses, focusing on the roles of microglia and astrocytes, their bidirectional communication with neurons, and their interaction with peripheral immune signals. We describe how various stimuli-including aging, protein aggregates, and cellular stress-modulate glial function and shift immune activity toward protective or deleterious outcomes. Special attention is given to endogenous regulatory pathways, including cytokine signaling, receptor-mediated crosstalk, and immunometabolic cues that determine the resolution or persistence of inflammation. We further discuss shared and disease-specific features of neuroinflammation across neurological disorders, offering a systems-level perspective on how immune activity contributes to neural resilience or degeneration. This integrated view aims to inform future studies on neuroimmune dynamics in health and disease.

摘要

神经炎症是一个动态的、依赖于环境的过程,在大脑发育、维持以及对损伤的反应中发挥着重要作用。它反映了一种精细平衡的神经免疫状态——在稳态条件下促进修复和适应,而在失调或长期激活时也会导致功能障碍。在这篇综述中,我们研究了神经炎症反应的细胞和分子机制,重点关注小胶质细胞和星形胶质细胞的作用、它们与神经元的双向通讯以及它们与外周免疫信号的相互作用。我们描述了包括衰老、蛋白质聚集体和细胞应激在内的各种刺激如何调节胶质细胞功能,并将免疫活动转向保护性或有害性结果。特别关注内源性调节途径,包括细胞因子信号传导、受体介导的串扰以及决定炎症消退或持续的免疫代谢线索。我们进一步讨论了神经系统疾病中神经炎症的共同特征和疾病特异性特征,从系统层面阐述了免疫活动如何影响神经弹性或退化。这种综合观点旨在为未来关于健康和疾病中神经免疫动力学的研究提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaf7/12404926/a2c5a674fc37/fimmu-16-1659947-g001.jpg

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