Pereira-Iglesias Marta, Maldonado-Teixido Joel, Melero Alejandro, Piriz Joaquin, Galea Elena, Ransohoff Richard M, Sierra Amanda
Achucarro Basque Center for Neuroscience, Leioa, Spain.
Department of Neuroscience, University of the Basque Country EHU/UPV, Leioa, Spain.
Nat Neurosci. 2025 Jan;28(1):15-23. doi: 10.1038/s41593-024-01818-w. Epub 2024 Dec 11.
Over a decade ago, it was discovered that microglia, the brain's immune cells, engulf synaptic material in a process named microglial pruning. This term suggests that microglia actively sculpt brain circuits by tagging and phagocytosing unwanted synapses. However, live imaging studies have yet to demonstrate how microglial synapse elimination occurs. To address this issue, we propose a new conceptual framework distinguishing between two potential mechanisms of synapse elimination, culling and scavenging. During culling, microglia may use a contractile ring to sever the neuronal plasma membrane, removing the unwanted synapse. During scavenging, synapse elimination is neuronal-driven, and the neuronal plasma membrane fission machinery sheds off synapses that are later phagocytosed by microglia. We will discuss the current limitations of studying microglial synapse elimination and evaluate evidence supporting either culling or scavenging. Discerning between these mechanisms is essential for determining the therapeutic value of phagocytosis modulators in diseases with altered brain connectivity.
十多年前,人们发现小胶质细胞,即大脑的免疫细胞,在一个名为小胶质细胞修剪的过程中吞噬突触物质。这个术语表明,小胶质细胞通过标记和吞噬不需要的突触来积极塑造大脑回路。然而,实时成像研究尚未证明小胶质细胞消除突触的过程是如何发生的。为了解决这个问题,我们提出了一个新的概念框架,区分突触消除的两种潜在机制,即剔除和清除。在剔除过程中,小胶质细胞可能会使用收缩环切断神经元质膜,去除不需要的突触。在清除过程中,突触消除是由神经元驱动的,神经元质膜裂变机制会脱落突触,随后这些突触会被小胶质细胞吞噬。我们将讨论目前研究小胶质细胞突触消除的局限性,并评估支持剔除或清除机制的证据。区分这些机制对于确定吞噬作用调节剂在大脑连接性改变的疾病中的治疗价值至关重要。