Exp Neurobiol.  2014 Dec;23(4):337-344. 10.5607/en.2014.23.4.337.

Exploring Myelin Dysfunction in Multiple System Atrophy

Affiliations
  • 1Neuroscience Research Australia, Sydney, NSW 2031, Australia. w.kim@unsw.edu.au
  • 2School of Medical Sciences, University of New South Wales, Sydney, NSW 2052, Australia.

Abstract

Multiple system atrophy (MSA) is a rare, yet fatal neurodegenerative disease that presents clinically with autonomic failure in combination with parkinsonism or cerebellar ataxia. MSA impacts on the autonomic nervous system affecting blood pressure, heart rate and bladder function, and the motor system affecting balance and muscle movement. The cause of MSA is unknown, no definitive risk factors have been identified, and there is no cure or effective treatment. The definitive pathology of MSA is the presence of alpha-synuclein aggregates in the brain and therefore MSA is classified as an alpha-synucleinopathy, together with Parkinson's disease and dementia with Lewy bodies. Although the molecular mechanisms of misfolding, fibrillation and aggregation of alpha-synuclein partly overlap with other alpha-synucleinopathies, the pathological pathway of MSA is unique in that the principal site for alpha-synuclein deposition is in the oligodendrocytes rather than the neurons. The sequence of pathological events of MSA is now recognized as abnormal protein redistributions in oligodendrocytes first, followed by myelin dysfunction and then neurodegeneration. Oligodendrocytes are responsible for the production and maintenance of myelin, the specialized lipid membrane that encases the axons of all neurons in the brain. Myelin is composed of lipids and two prominent proteins, myelin basic protein and proteolipid protein. In vitro studies suggest that aberration in protein distribution and lipid transport may lead to myelin dysfunction in MSA. The purpose of this perspective is to bring together available evidence to explore the potential role of alpha-synuclein, myelin protein dysfunction, lipid dyshomeostasis and ABCA8 in MSA pathogenesis.

Keyword

Multiple system atrophy; oligodendrocyte; alpha-synuclein; myelin; lipid dyshomeostasis

MeSH Terms

alpha-Synuclein
Autonomic Nervous System
Axons
Blood Pressure
Brain
Cerebellar Ataxia
Dementia
Heart Rate
Lewy Bodies
Membranes
Multiple System Atrophy*
Myelin Proteins
Myelin Sheath*
Neurodegenerative Diseases
Neurons
Oligodendroglia
Parkinson Disease
Parkinsonian Disorders
Pathology
Risk Factors
Urinary Bladder
Myelin Proteins
alpha-Synuclein
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