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轴突起始段相关小胶质细胞。

Axon initial segment-associated microglia.

作者信息

Baalman Kelli, Marin Miguel A, Ho Tammy Szu-Yu, Godoy Marlesa, Cherian Leela, Robertson Claudia, Rasband Matthew N

机构信息

Department of Neuroscience.

Program in Developmental Biology, and.

出版信息

J Neurosci. 2015 Feb 4;35(5):2283-92. doi: 10.1523/JNEUROSCI.3751-14.2015.

Abstract

Microglia are the brain's resident immune cells and function as the main defense against pathogens or injury. However, in the absence of disease, microglia have other functions in the normal brain. For example, previous studies showed that microglia contribute to circuit refinement and synaptic plasticity in the developing and adult brain, respectively. Thus, microglia actively participate in regulating neuronal excitability and function. Here, we report that in the cortex, but not other brain regions, a subset of microglia extend a single process that specifically associates and overlaps with the axon initial segment (AIS), the site where action potentials are generated. Similar associations were not observed with dendrites or distal axons. Microglia-AIS interactions appear early in development, persist throughout adulthood, and are conserved across species including mice, rats, and primates. However, these interactions are lost after microglial activation following brain injury, suggesting that such interactions may be part of healthy brain function. Loss of microglial CX3CR1 receptors, or the specialized extracellular matrix surrounding the AIS, did not disrupt the interaction. However, loss of AIS proteins by the neuron-specific deletion of the master AIS scaffold AnkyrinG disrupted microglia-AIS interactions. These results reveal a unique population of microglia that specifically interact with the AIS in the adult cortex.

摘要

小胶质细胞是大脑中的常驻免疫细胞,是抵御病原体或损伤的主要防线。然而,在没有疾病的情况下,小胶质细胞在正常大脑中还有其他功能。例如,先前的研究表明,小胶质细胞分别在发育中的大脑和成年大脑中促进神经回路的优化和突触可塑性。因此,小胶质细胞积极参与调节神经元的兴奋性和功能。在此,我们报告,在皮层而非其他脑区,一部分小胶质细胞伸出单个突起,该突起与轴突起始段(AIS)特异性关联并重叠,轴突起始段是动作电位产生的部位。在树突或轴突远端未观察到类似的关联。小胶质细胞与轴突起始段的相互作用在发育早期出现,在成年期持续存在,并且在包括小鼠、大鼠和灵长类动物在内的物种中保守。然而,脑损伤后小胶质细胞激活会导致这些相互作用消失,这表明此类相互作用可能是健康脑功能的一部分。小胶质细胞CX3CR1受体的缺失,或轴突起始段周围的特殊细胞外基质的缺失,均未破坏这种相互作用。然而,通过神经元特异性缺失主要的轴突起始段支架锚蛋白G导致轴突起始段蛋白缺失,会破坏小胶质细胞与轴突起始段的相互作用。这些结果揭示了在成年皮层中与轴突起始段特异性相互作用的独特小胶质细胞群体。

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Axon initial segment-associated microglia.轴突起始段相关小胶质细胞。
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