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脑膜淋巴管-小胶质细胞轴调节突触生理学。

Meningeal lymphatics-microglia axis regulates synaptic physiology.

作者信息

Kim Kyungdeok, Abramishvili Daviti, Du Siling, Papadopoulos Zachary, Cao Jay, Herz Jasmin, Smirnov Igor, Thomas Jean-Leon, Colonna Marco, Kipnis Jonathan

机构信息

Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.

Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.

出版信息

Cell. 2025 May 15;188(10):2705-2719.e23. doi: 10.1016/j.cell.2025.02.022. Epub 2025 Mar 21.

Abstract

Meningeal lymphatics serve as an outlet for cerebrospinal fluid, and their dysfunction is associated with various neurodegenerative conditions. Previous studies have demonstrated that dysfunctional meningeal lymphatics evoke behavioral changes, but the neural mechanisms underlying these changes have remained elusive. Here, we show that prolonged impairment of meningeal lymphatics alters the balance of cortical excitatory and inhibitory synaptic inputs, accompanied by deficits in memory tasks. These synaptic and behavioral alterations induced by lymphatic dysfunction are mediated by microglia, leading to increased expression of the interleukin 6 gene (Il6). IL-6 drives inhibitory synapse phenotypes via a combination of trans- and classical IL-6 signaling. Restoring meningeal lymphatic function in aged mice reverses age-associated synaptic and behavioral alterations. Our findings suggest that dysfunctional meningeal lymphatics adversely impact cortical circuitry through an IL-6-dependent mechanism and identify a potential target for treating aging-associated cognitive decline.

摘要

脑膜淋巴管是脑脊液的一个排泄途径,其功能障碍与多种神经退行性疾病相关。以往的研究表明,功能失调的脑膜淋巴管会引发行为改变,但其背后的神经机制仍不清楚。在这里,我们表明,脑膜淋巴管的长期损伤会改变皮质兴奋性和抑制性突触输入的平衡,并伴有记忆任务缺陷。由淋巴管功能障碍引起的这些突触和行为改变是由小胶质细胞介导的,导致白细胞介素6基因(Il6)的表达增加。IL-6通过跨膜和经典IL-6信号传导的组合驱动抑制性突触表型。恢复老年小鼠的脑膜淋巴管功能可逆转与年龄相关的突触和行为改变。我们的研究结果表明,功能失调的脑膜淋巴管通过IL-6依赖性机制对皮质回路产生不利影响,并确定了治疗与衰老相关的认知衰退的潜在靶点。

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