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

被引:7
作者
Cangalaya, Carla [1 ]
Sun, Weilun [1 ,2 ]
Stoyanov, Stoyan [1 ]
Dunay, Ildiko Rita [3 ,4 ]
Dityatev, Alexander [1 ,4 ,5 ]
机构
[1] German Ctr Neurodegenerat Dis DZNE, Mol Neuroplast Grp, Leipziger Str 44,Haus64, D-39120 Magdeburg, Germany
[2] Jilin Univ, Sch Pharmaceut Sci, Dept Pharmacol, Changchun, Peoples R China
[3] Otto von Guericke Univ, Inst Inflammat & Neurodegenerat, Magdeburg, Germany
[4] Ctr Behav Brain Sci CBBS, Magdeburg, Germany
[5] Otto von Guericke Univ, Med Fac, Magdeburg, Germany
基金
中国国家自然科学基金;
关键词
C1q; C3; complement protein; extracellular matrix; microglia; spine; synapse; two-photon microscopy; CHONDROITIN SULFATE PROTEOGLYCAN; STRUCTURAL PLASTICITY; SPINAL-CORD; BRAIN; PROMOTES; ABC; COLOCALIZATION; ELIMINATION; MOLECULES; TISSUE;
D O I
10.1002/glia.24588
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. Enzymatic digestion of extracellular matrix increased microglial branching complexity and dendritic spine density. This correlated with reduced C1q deposition, shorter microglia contacts with synapses, and impaired synaptic elimination by microglia. image
引用
收藏
页码:1874 / 1892
页数:19
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