Synucleinopathy alters nanoscale organization and diffusion in the brain extracellular space through hyaluronan remodeling.
Federico N SoriaChiara PavioloEvelyne DoudnikoffMarie-Laure ArotcarenaAntony LeeNoémie DannéAmit Kumar MandalPhilippe GossetBenjamin DehayLaurent GrocLaurent CognetErwan BezardPublished in: Nature communications (2020)
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.
Keyphrases
- resting state
- white matter
- extracellular matrix
- functional connectivity
- atomic force microscopy
- cerebral ischemia
- high resolution
- single cell
- electron microscopy
- multiple sclerosis
- skeletal muscle
- brain injury
- oxidative stress
- metabolic syndrome
- adipose tissue
- subarachnoid hemorrhage
- young adults
- high fat diet induced
- stress induced
- high speed
- data analysis