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小胶质细胞耗竭会增加小鼠大脑弥漫性和聚集性细胞外基质中聚集蛋白聚糖和透明质酸的水平。

Microglial depletion increases aggrecan and hyaluronan levels in the diffuse and aggregated extracellular matrix of the mouse brain.

作者信息

Egorova Diana, Kerever Aurelien, Inada Masaki, Itoh Yoshifumi, Arikawa-Hirasawa Eri, Miyata Shinji

机构信息

Graduate School of Agriculture, Tokyo University of Agriculture and Technology, 3-5-8 Saiwaicho, Fuchu, Tokyo, 183-8509, Japan.

Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, Tokyo, 113-8421, Japan.

出版信息

Sci Rep. 2025 Mar 18;15(1):9376. doi: 10.1038/s41598-025-94224-6.

Abstract

The extracellular matrix (ECM) in the brain can be divided into aggregated ECM, such as perineuronal nets (PNNs) around neurons, and diffuse ECM, which is present throughout the brain parenchyma. Both aggregated and diffuse ECM restrict synaptic plasticity and stabilize neural circuits in the adult brain. Hyaluronan (HA) acts as a scaffold for the brain ECM, and multiple proteoglycans, such as aggrecan, bind to HA to form a macromolecular complex. Recent evidence suggests that microglia, the resident immune cells of the brain, play a crucial role in ECM homeostasis. However, it remains unclear how microglia influence the molecular composition of the ECM. Using a tissue-clearing technique and histochemical analysis, we found that microglial depletion increased the staining intensity of aggrecan and HA in both PNNs and diffuse ECM. Biochemical analyses further confirmed the accumulation of the aggrecan core protein and HA following microglial depletion. Our findings highlight the essential role of microglia in regulating the ECM composition and provide new insights into the mechanisms by which microglia influence neuronal function.

摘要

大脑中的细胞外基质(ECM)可分为聚集型ECM,如神经元周围的神经周网(PNN),以及弥漫型ECM,其存在于整个脑实质中。聚集型和弥漫型ECM在成人大脑中均会限制突触可塑性并稳定神经回路。透明质酸(HA)作为大脑ECM的支架,多种蛋白聚糖,如聚集蛋白聚糖,与HA结合形成大分子复合物。最近的证据表明,小胶质细胞作为大脑中的常驻免疫细胞,在ECM动态平衡中起着至关重要的作用。然而,小胶质细胞如何影响ECM的分子组成仍不清楚。通过组织透明化技术和组织化学分析,我们发现小胶质细胞耗竭会增加PNN和弥漫型ECM中聚集蛋白聚糖和HA的染色强度。生化分析进一步证实了小胶质细胞耗竭后聚集蛋白聚糖核心蛋白和HA的积累。我们的研究结果突出了小胶质细胞在调节ECM组成中的重要作用,并为小胶质细胞影响神经元功能的机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a9f/11920245/612dfb29d8b0/41598_2025_94224_Fig1_HTML.jpg

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