Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, 33076, Bordeaux, France.
Centre National de la Recherche Scientifique, IMN, UMR 5293, 33076, Bordeaux, France.
Nat Commun. 2020 Jul 10;11(1):3440. doi: 10.1038/s41467-020-17328-9.
In recent years, exploration of the brain extracellular space (ECS) has made remarkable progress, including nanoscopic characterizations. However, whether ECS precise conformation is altered during brain pathology remains unknown. Here we study the nanoscale organization of pathological ECS in adult mice under degenerative conditions. Using electron microscopy in cryofixed tissue and single nanotube tracking in live brain slices combined with super-resolution imaging analysis, we find enlarged ECS dimensions and increased nanoscale diffusion after α-synuclein-induced neurodegeneration. These animals display a degraded hyaluronan matrix in areas close to reactive microglia. Furthermore, experimental hyaluronan depletion in vivo reduces dopaminergic cell loss and α-synuclein load, induces microgliosis and increases ECS diffusivity, highlighting hyaluronan as diffusional barrier and local tissue organizer. These findings demonstrate the interplay of ECS, extracellular matrix and glia in pathology, unraveling ECS features relevant for the α-synuclein propagation hypothesis and suggesting matrix manipulation as a disease-modifying strategy.
近年来,对脑细胞外空间(ECS)的探索取得了显著进展,包括纳米级特征。然而,在脑病理过程中 ECS 的精确构象是否发生改变尚不清楚。在这里,我们研究了退行性条件下成年小鼠病理性 ECS 的纳米级组织。我们使用冷冻固定组织中的电子显微镜和活脑切片中的单纳米管跟踪技术结合超分辨率成像分析,发现α-突触核蛋白诱导的神经退行性变后 ECS 尺寸增大,纳米级扩散增加。这些动物在靠近反应性小胶质细胞的区域表现出透明质酸基质降解。此外,体内实验性透明质酸耗竭可减少多巴胺能神经元丢失和α-突触核蛋白负荷,诱导小胶质细胞增生并增加 ECS 扩散率,突出了透明质酸作为扩散屏障和局部组织组织者的作用。这些发现表明了 ECS、细胞外基质和胶质细胞在病理学中的相互作用,揭示了与α-突触核蛋白传播假说相关的 ECS 特征,并提示基质操纵作为一种疾病修饰策略。