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神经元作为免疫调节因子:从快速神经活动到细胞因子和小胶质细胞的长期调节

Neurons as Immunomodulators: From Rapid Neural Activity to Prolonged Regulation of Cytokines and Microglia.

作者信息

Wood Levi B, Singer Annabelle C

机构信息

Wallace H. Coulter Department of Biomedical Engineering, George W. Woodruff School of Mechanical Engineering and Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia, USA; email:

出版信息

Annu Rev Biomed Eng. 2025 May;27(1):55-72. doi: 10.1146/annurev-bioeng-110122-120158. Epub 2025 Jan 13.

Abstract

Regulation of the brain's neuroimmune system is central to development, normal function, and disease. Neuronal communication to microglia, the primary immune cells of the brain, is well known to involve purinergic signaling mediated via ATP secretion and the cytokine fractalkine. Recent evidence shows that neurons release multiple cytokines beyond fractalkine, yet these are less studied and poorly understood. In contrast to ATP, cytokines are a class of signaling molecule that are much larger, with longer signaling and farther diffusion. We posit that neuron-expressed cytokines are an essential mechanism of neuron-microglia communication that arises as part of both normal learning and memory and in response to tissue pathology. Thus, neurons are underappreciated immunomodulatory cells that express diverse immunomodulatory signals. While neuronally sourced cytokines have been understudied, new technical advances make this a timely topic. The goal of this review is to define what is known about the cytokines expressed from neurons, how they are regulated, and the effects of these cytokines on microglia. We delineate key knowledge gaps and needs for new tools to define and analyze neuronal roles in immunomodulation. Given that cytokines are central regulators of microglial function, a broad new body of work is required to illuminate functional links between these neuronally expressed cytokines and sustained and transient microglial function.

摘要

大脑神经免疫系统的调节对于发育、正常功能及疾病至关重要。神经元与大脑主要免疫细胞小胶质细胞之间的通讯,众所周知涉及通过ATP分泌和细胞因子趋化因子介导的嘌呤能信号传导。最近的证据表明,神经元除了释放趋化因子外,还会释放多种细胞因子,但对这些细胞因子的研究较少且了解不足。与ATP不同,细胞因子是一类更大的信号分子,具有更长的信号传导和更远的扩散距离。我们认为,神经元表达的细胞因子是神经元-小胶质细胞通讯的一种重要机制,它在正常学习和记忆过程中以及对组织病理学的反应中都会出现。因此,神经元作为表达多种免疫调节信号的免疫调节细胞,一直未得到充分重视。虽然对神经元来源的细胞因子研究较少,但新的技术进展使这个话题变得及时。这篇综述的目的是明确关于神经元表达的细胞因子的已知信息、它们是如何被调节的,以及这些细胞因子对小胶质细胞的影响。我们阐述了关键的知识空白以及对定义和分析神经元在免疫调节中作用的新工具的需求。鉴于细胞因子是小胶质细胞功能的核心调节因子,需要大量新的研究工作来阐明这些神经元表达的细胞因子与小胶质细胞持续和短暂功能之间的功能联系。

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