Increased neuronal α-synuclein pathology associates with its accumulation in oligodendrocytes in mice modeling α-synucleinopathies.
Multiple system atrophy (MSA) is a progressive neurodegenerative disorder characterized by striatonigral degeneration and olivo-pontocerebellar atrophy. The histopathological hallmark of MSA is glial cytoplasmic inclusions (GCI) within oligodendrocytes, accompanied by neuronal degeneration. MSA is a...
Main Authors: | Haya Kisos, Katharina Pukaß, Tamir Ben-Hur, Christiane Richter-Landsberg, Ronit Sharon |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2012-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3471961?pdf=render |
Similar Items
-
Higher levels of myelin phospholipids in brains of neuronal α-Synuclein transgenic mice precede myelin loss
by: Jessica Grigoletto, et al.
Published: (2017-05-01) -
Inhibition of UCH-L1 in oligodendroglial cells results in microtubule stabilization and prevents α-synuclein aggregate formation by activating the autophagic pathway: implications for multiple system atrophy
by: Katharina ePukaß, et al.
Published: (2015-05-01) -
The Interplay between α-Synuclein and Microglia in α-Synucleinopathies
by: Jacob S. Deyell, et al.
Published: (2023-01-01) -
α-Synuclein pathology in post-mortem retina and optic nerve is specific for α-synucleinopathies
by: Frederique J. Hart de Ruyter, et al.
Published: (2023-08-01) -
Pathological α-synuclein detected by real-time quaking-induced conversion in synucleinopathies
by: Juan Huang, et al.
Published: (2024-03-01)