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Open AccessJournal ArticleDOI

Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms.

Marjo S. van der Knaap, +1 more
- 01 Sep 2017 - 
- Vol. 134, Iss: 3, pp 351-382
TLDR
A novel classification of leukodystrophies is proposed that takes into account the primary involvement of any white matter component, and Categories in this classification are the myelin disorders due to a primary defect in oligodendrocytes or myelin; astrocytopathies; leuko-axonopathies; microgliopathy; andLeuko-vasculopathies.
Abstract
Leukodystrophies are genetically determined disorders characterized by the selective involvement of the central nervous system white matter. Onset may be at any age, from prenatal life to senescence. Many leukodystrophies are degenerative in nature, but some only impair white matter function. The clinical course is mostly progressive, but may also be static or even improving with time. Progressive leukodystrophies are often fatal, and no curative treatment is known. The last decade has witnessed a tremendous increase in the number of defined leukodystrophies also owing to a diagnostic approach combining magnetic resonance imaging pattern recognition and next generation sequencing. Knowledge on white matter physiology and pathology has also dramatically built up. This led to the recognition that only few leukodystrophies are due to mutations in myelin- or oligodendrocyte-specific genes, and many are rather caused by defects in other white matter structural components, including astrocytes, microglia, axons and blood vessels. We here propose a novel classification of leukodystrophies that takes into account the primary involvement of any white matter component. Categories in this classification are the myelin disorders due to a primary defect in oligodendrocytes or myelin (hypomyelinating and demyelinating leukodystrophies, leukodystrophies with myelin vacuolization); astrocytopathies; leuko-axonopathies; microgliopathies; and leuko-vasculopathies. Following this classification, we illustrate the neuropathology and disease mechanisms of some leukodystrophies taken as example for each category. Some leukodystrophies fall into more than one category. Given the complex molecular and cellular interplay underlying white matter pathology, recognition of the cellular pathology behind a disease becomes crucial in addressing possible treatment strategies.

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Citations
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Myelin in the Central Nervous System: Structure, Function, and Pathology.

TL;DR: The biology of myelin, the expanded relationship of myelinating oligodendrocytes with its underlying axons and the neighboring cells, and its disturbances in various diseases such as multiple sclerosis, acute disseminated encephalomyelitis, and neuromyELitis optica spectrum disorders are reviewed.
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White matter degeneration in vascular and other ageing-related dementias

TL;DR: It is demonstrated that WM degeneration encompasses multiple substrates and therefore more than one pharmacological approach is necessary to preserve axonal function and prevent cognitive impairment.
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CSF1R-related leukoencephalopathy: A major player in primary microgliopathies

TL;DR: The current knowledge of CSF1R-related leukoencephalopathy is addressed and the putative pathophysiology is discussed, with a focus on microglia, as well as future research directions.
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Astrocyte and Oligodendrocyte Cross-Talk in the Central Nervous System.

TL;DR: Emerging evidence of astrocyte-oligodendrocytes communication in health and disease is reviewed to reveal important insights into the pathogenesis and treatment of CNS diseases.
References
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Journal ArticleDOI

Panglial Gap Junctional Communication is Essential for Maintenance of Myelin in the CNS

TL;DR: Histological and ultrastructural analyses revealed severe vacuolization and myelination defects in all white matter tracts of the CNS, and Cx30/Cx47 double-deficient mice exhibited a decreased number of oligodendrocytes, severe astrogliosis, and microglial activation in white matter tract, showing that both connexins are required for maintenance of myelin.
Journal ArticleDOI

Galectin-3 drives oligodendrocyte differentiation to control myelin integrity and function.

TL;DR: Exposure to galectin-3 promoted OLG differentiation in a dose- and carbohydrate-dependent fashion consistent with the ‘glycosylation signature’ of immature versus differentiated OLG, thus contributing to myelin integrity and function with critical implications in the recovery of inflammatory demyelinating disorders.
Journal ArticleDOI

Netrin 1 and Dcc regulate oligodendrocyte process branching and membrane extension via Fyn and RhoA

TL;DR: A novel role for the chemotropic guidance cue netrin 1 and its receptor deleted in colorectal carcinoma (Dcc) in the remodeling of oligodendrocyte processes is described and a requirement for Src family kinase activity downstream of netrin-1-dependent process extension and branching is identified.
Journal ArticleDOI

Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus

TL;DR: In three patients of two Cree families, a homozygous missense mutation resulting in a histidine substitution at arginine 195 of ε‐eIF2B is found in the brain of affected individuals.
Journal ArticleDOI

Giant axonal neuropathy-associated gigaxonin mutations impair intermediate filament protein degradation.

TL;DR: It is demonstrated that gigaxonin was responsible for the degradation of vimentin IFs and proteasome inhibition by MG-132 reversed the clearance of IF proteins in cells overexpressing gigax onin, demonstrating the involvement of the proteasomal degradation pathway.
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