Achucarro Basque Center for Neuroscience, Parque Científico, University of the Basque Country (UPV/EHU), Leioa, Spain.
Department of Neuroscience, University of the Basque Country (UPV/EHU), Leioa, Spain.
Front Immunol. 2020 Mar 27;11:506. doi: 10.3389/fimmu.2020.00506. eCollection 2020.
From development to aging and disease, the brain parenchyma is under the constant threat of debris accumulation, in the form of dead cells and protein aggregates. To prevent garbage buildup, the brain is equipped with efficient phagocytes: the microglia. Microglia are similar, but not identical to other tissue macrophages, and in this review, we will first summarize the differences in the origin, lineage and population maintenance of microglia and macrophages. Then, we will discuss several principles that govern macrophage phagocytosis of apoptotic cells (efferocytosis), including the existence of redundant recognition mechanisms ("find-me" and "eat-me") that lead to a tight coupling between apoptosis and phagocytosis. We will then describe that resulting from engulfment and degradation of apoptotic cargo, phagocytes undergo an epigenetic, transcriptional and metabolic rewiring that leads to trained immunity, and discuss its relevance for microglia and brain function. In summary, we will show that neuroimmunologists can learn many lessons from the well-developed field of macrophage phagocytosis biology.
从发育到衰老和疾病,脑实质一直受到以死细胞和蛋白质聚集体形式存在的碎片积累的威胁。为了防止垃圾堆积,大脑配备了高效的吞噬细胞:小胶质细胞。小胶质细胞与其他组织巨噬细胞相似,但又不完全相同,在这篇综述中,我们首先将总结小胶质细胞和巨噬细胞在起源、谱系和群体维持方面的差异。然后,我们将讨论几个控制巨噬细胞吞噬凋亡细胞(吞噬作用)的原则,包括存在冗余的识别机制(“找我”和“吃我”),这些机制导致凋亡和吞噬作用紧密偶联。然后,我们将描述吞噬和降解凋亡货物后吞噬细胞经历的表观遗传、转录和代谢重编程,导致训练免疫,并讨论其与小胶质细胞和大脑功能的相关性。总之,我们将表明神经免疫学家可以从小胶质细胞吞噬作用生物学这一成熟领域学到很多经验。