de Deus Junia Lara, Faborode Oluwaseun Samuel, Nandi Sayan
Department of Anatomy, Howard University College of Medicine, Washington, DC, USA.
Dev Neurosci. 2024 Sep 12:1-21. doi: 10.1159/000541379.
Neural circuits are subjected to refinement throughout life. The dynamic addition and elimination (pruning) of synapses are necessary for maturation of neural circuits and synaptic plasticity. Due to their phagocytic nature, microglia have been considered as the primary mediators of synaptic pruning. Synaptic pruning can strengthen an active synapse by removing excess weaker synapses during development. Inappropriate synaptic pruning can often influence a disease outcome or an injury response.
This review offers a focused discussion on microglial roles in synaptic pruning, based on the evidence gathered from genetic manipulations in mice. Genetically labeled microglia and synapses often allow assessment of their interactions in real time. Further manipulations involving synaptically localized molecules, neuronally or glial-derived diffusible factors, and their respective cognate receptors in microglia provide critical evidence in support of a direct role of microglia in synaptic pruning.
We discuss microglial contact-dependent "eat-me," "don't-eat-me," and "find-me" signals, as well as recently identified noncontact pruning, under the contexts of neural circuit, brain region, developmental window, and an injury or a disease state.
神经回路在整个生命过程中都会经历精细化过程。突触的动态添加和消除(修剪)对于神经回路的成熟和突触可塑性是必要的。由于小胶质细胞具有吞噬特性,它们被认为是突触修剪的主要介质。在发育过程中,突触修剪可以通过去除多余的较弱突触来强化活跃的突触。不适当的突触修剪常常会影响疾病的转归或损伤反应。
本综述基于从小鼠基因操作中收集的证据,重点讨论了小胶质细胞在突触修剪中的作用。基因标记的小胶质细胞和突触通常允许实时评估它们之间的相互作用。进一步涉及突触定位分子、神经元或胶质细胞衍生的可扩散因子以及它们在小胶质细胞中各自的同源受体的操作,为支持小胶质细胞在突触修剪中的直接作用提供了关键证据。
我们在神经回路、脑区、发育窗口以及损伤或疾病状态的背景下,讨论小胶质细胞接触依赖性的“吃掉我”“别吃掉我”和“找到我”信号,以及最近发现的非接触性修剪。