Integrity of neural extracellular matrix is required for microglia-mediated synaptic remodeling

IF 5.4 2区 医学 Q1 NEUROSCIENCES
Glia Pub Date : 2024-06-30 DOI:10.1002/glia.24588
Carla Cangalaya, Weilun Sun, Stoyan Stoyanov, Ildiko Rita Dunay, Alexander Dityatev
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引用次数: 0

Abstract

Microglia continuously remodel synapses, which are embedded in the extracellular matrix (ECM). However, the mechanisms, which govern this process remain elusive. To investigate the influence of the neural ECM in synaptic remodeling by microglia, we disrupted ECM integrity by injection of chondroitinase ABC (ChABC) into the retrosplenial cortex of healthy adult mice. Using in vivo two-photon microscopy we found that ChABC treatment increased microglial branching complexity and ECM phagocytic capacity and decreased spine elimination rate under basal conditions. Moreover, ECM attenuation largely prevented synaptic remodeling following synaptic stress induced by photodamage of single synaptic elements. These changes were associated with less stable and smaller microglial contacts at the synaptic damage sites, diminished deposition of calreticulin and complement proteins C1q and C3 at synapses and impaired expression of microglial CR3 receptor. Thus, our findings provide novel insights into the function of the neural ECM in deposition of complement proteins and synaptic remodeling by microglia.

Abstract Image

小胶质细胞介导的突触重塑需要神经细胞外基质的完整性。
小胶质细胞不断重塑嵌入细胞外基质(ECM)中的突触。然而,支配这一过程的机制仍然难以捉摸。为了研究神经 ECM 对小胶质细胞重塑突触的影响,我们向健康成年小鼠的后脾皮层注射了软骨素酶 ABC(ChABC),从而破坏了 ECM 的完整性。通过使用体内双光子显微镜,我们发现 ChABC 处理增加了小胶质细胞分支的复杂性和 ECM 吞噬能力,并降低了基础条件下脊柱的消除率。此外,ECM 的衰减在很大程度上阻止了单个突触元件光损伤诱导的突触应激后的突触重塑。这些变化与以下因素有关:突触损伤部位的小胶质细胞接触更不稳定,接触面积更小,钙网蛋白和补体蛋白 C1q 和 C3 在突触处的沉积减少,以及小胶质细胞 CR3 受体的表达受损。因此,我们的研究结果为了解神经 ECM 在小胶质细胞沉积补体蛋白和突触重塑中的功能提供了新的视角。
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来源期刊
Glia
Glia 医学-神经科学
CiteScore
13.10
自引率
4.80%
发文量
162
审稿时长
3-8 weeks
期刊介绍: GLIA is a peer-reviewed journal, which publishes articles dealing with all aspects of glial structure and function. This includes all aspects of glial cell biology in health and disease.
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