白细胞介素-1 对神经网络的调节

Brain plasticity (Amsterdam, Netherlands) Pub Date : 2021-08-23 eCollection Date: 2021-01-01 DOI:10.3233/BPL-200109
Daniel P Nemeth, Ning Quan
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摘要

白细胞介素-1(IL-1)是一种炎性细胞因子,已被证明可在平衡和疾病中调节神经元信号。在平衡状态下,IL-1 可调节睡眠和记忆的形成,而在疾病中,IL-1 会损害记忆并改变情感。有趣的是,IL-1 能引起行为的长期变化,这表明 IL-1 能改变神经可塑性。IL-1的神经可塑性效应是通过其同源受体白介素-1 1型受体(IL-1R1)介导的,并取决于IL-1R1表达的分布和细胞类型。最近的报告发现,IL-1R1 的表达局限于神经元、星形胶质细胞和内皮细胞的离散亚群,这表明 IL-1 可直接通过神经元 IL-1R1 或间接通过非神经元 IL-1R1 影响神经回路。在这篇综述中,我们根据最新文献分析了IL-1/IL-1R1信号可能影响神经可塑性的多种机制,并提供了可能的解释,以澄清过去报道的不一致和令人困惑的研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Modulation of Neural Networks by Interleukin-1.

Interleukin-1 (IL-1) is an inflammatory cytokine that has been shown to modulate neuronal signaling in homeostasis and diseases. In homeostasis, IL-1 regulates sleep and memory formation, whereas in diseases, IL-1 impairs memory and alters affect. Interestingly, IL-1 can cause long-lasting changes in behavior, suggesting IL-1 can alter neuroplasticity. The neuroplastic effects of IL-1 are mediated via its cognate receptor, Interleukin-1 Type 1 Receptor (IL-1R1), and are dependent on the distribution and cell type(s) of IL-1R1 expression. Recent reports found that IL-1R1 expression is restricted to discrete subpopulations of neurons, astrocytes, and endothelial cells and suggest IL-1 can influence neural circuits directly through neuronal IL-1R1 or indirectly via non-neuronal IL-1R1. In this review, we analyzed multiple mechanisms by which IL-1/IL-1R1 signaling might impact neuroplasticity based upon the most up-to-date literature and provided potential explanations to clarify discrepant and confusing findings reported in the past.

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