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小胶质细胞通过去除抑制性突触来实现跨模态可塑性。

Microglia enable cross-modal plasticity by removing inhibitory synapses.

机构信息

Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

KOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, Osaka University, Suita 565-0871, Japan.

出版信息

Cell Rep. 2023 May 30;42(5):112383. doi: 10.1016/j.celrep.2023.112383. Epub 2023 Apr 21.

Abstract

Cross-modal plasticity is the repurposing of brain regions associated with deprived sensory inputs to improve the capacity of other sensory modalities. The functional mechanisms of cross-modal plasticity can indicate how the brain recovers from various forms of injury and how different sensory modalities are integrated. Here, we demonstrate that rewiring of the microglia-mediated local circuit synapse is crucial for cross-modal plasticity induced by visual deprivation (monocular deprivation [MD]). MD relieves the usual inhibition of functional connectivity between the somatosensory cortex and secondary lateral visual cortex (V2L). This results in enhanced excitatory responses in V2L neurons during whisker stimulation and a greater capacity for vibrissae sensory discrimination. The enhanced cross-modal response is mediated by selective removal of inhibitory synapse terminals on pyramidal neurons by the microglia in the V2L via matrix metalloproteinase 9 signaling. Our results provide insights into how cortical circuits integrate different inputs to functionally compensate for neuronal damage.

摘要

跨模态可塑性是指重新分配与剥夺感觉输入相关的大脑区域,以提高其他感觉模态的能力。跨模态可塑性的功能机制可以说明大脑如何从各种形式的损伤中恢复,以及不同感觉模态如何整合。在这里,我们证明了小胶质细胞介导的局部回路突触的重新布线对于视觉剥夺(单眼剥夺[MD])诱导的跨模态可塑性至关重要。MD 缓解了体感皮层和次级外侧视觉皮层(V2L)之间功能连接的通常抑制。这导致在胡须刺激期间 V2L 神经元的兴奋性反应增强,并且对触须感觉的辨别能力更强。通过基质金属蛋白酶 9 信号,V2L 中的小胶质细胞选择性地去除锥体神经元上的抑制性突触末梢,从而介导增强的跨模态反应。我们的结果提供了有关皮质回路如何整合不同输入以功能上补偿神经元损伤的见解。

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