Augusto-Oliveira Marcus, Arrifano Gabriela de Paula, Leal-Nazaré Caio Gustavo, Chaves-Filho Adriano, Santos-Sacramento Leticia, Lopes-Araujo Amanda, Tremblay Marie-Ève, Crespo-Lopez Maria Elena
Laboratório de Farmacologia Molecular, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil; Amazonian Institute on Mercury (Instituto Amazônico do Mercúrio - IAMER).
Laboratório de Farmacologia Molecular, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil; Amazonian Institute on Mercury (Instituto Amazônico do Mercúrio - IAMER).
Neurosci Biobehav Rev. 2025 May;172:106091. doi: 10.1016/j.neubiorev.2025.106091. Epub 2025 Mar 4.
Microglia are the brain resident macrophages that respond rapidly to any insult. These non-neuroectodermal cells are decorated with plenty of receptors allowing them to recognise and respond precisely to a multitude of stimuli. To do so, microglia undergo structural and functional changes aiming to actively keep the brain's homeostasis. However, some microglial responses, when sustained or exacerbated, can contribute to neuropathology and neurodegeneration. Many microglial molecular and cellular changes were identified that display a strong correlation with neuronal damage and neuroinflammation/disease status, as well as present key sex-related differences that modulate microglial outcomes. Nevertheless, the relationship between microglial structural and functional features is just beginning to be unravelled. Several reports show that microglia undergo soma and branch remodelling in response to environmental stimuli, ageing, neurodegenerative diseases, trauma, and systemic inflammation, suggesting a complex form and function link. Also, it is reasonable overall to suppose that microglia diminishing their process length and ramification also reduce their monitoring activity of synapses, which is critical for detecting any synaptic disturbance and performing synaptic remodelling. Elucidating the complex interactions between microglial morphological plasticity and its functional implications appears essential for the understanding of complex cognitive and behavioural processes in health and neuropathological conditions.
小胶质细胞是驻留在大脑中的巨噬细胞,对任何损伤都能迅速做出反应。这些非神经外胚层细胞配备有大量受体,使它们能够精确识别并对多种刺激做出反应。为此,小胶质细胞会发生结构和功能上的变化,旨在积极维持大脑的稳态。然而,一些小胶质细胞反应如果持续或加剧,可能会导致神经病理学和神经退行性变。已发现许多小胶质细胞的分子和细胞变化与神经元损伤、神经炎症/疾病状态密切相关,并且存在调节小胶质细胞结果的关键性别相关差异。尽管如此,小胶质细胞结构和功能特征之间的关系才刚刚开始被揭示。一些报告表明,小胶质细胞会响应环境刺激、衰老、神经退行性疾病、创伤和全身炎症而发生胞体和分支重塑,这表明存在复杂的形态与功能联系。此外,总体而言有理由认为,小胶质细胞缩短其突起长度和分支也会降低其对突触的监测活动,而这对于检测任何突触紊乱和进行突触重塑至关重要。阐明小胶质细胞形态可塑性与其功能影响之间的复杂相互作用,对于理解健康和神经病理状态下的复杂认知和行为过程似乎至关重要。