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Published in: Journal of Neuroinflammation 1/2017

Open Access 01-12-2017 | Research

Absence of system xc on immune cells invading the central nervous system alleviates experimental autoimmune encephalitis

Authors: Ellen Merckx, Giulia Albertini, Magdalena Paterka, Cathy Jensen, Philipp Albrecht, Michael Dietrich, Joeri Van Liefferinge, Eduard Bentea, Lise Verbruggen, Thomas Demuyser, Lauren Deneyer, Jan Lewerenz, Geert van Loo, Jacques De Keyser, Hideyo Sato, Pamela Maher, Axel Methner, Ann Massie

Published in: Journal of Neuroinflammation | Issue 1/2017

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Abstract

Background

Multiple sclerosis (MS) is an autoimmune demyelinating disease that affects the central nervous system (CNS), leading to neurodegeneration and chronic disability. Accumulating evidence points to a key role for neuroinflammation, oxidative stress, and excitotoxicity in this degenerative process. System xc or the cystine/glutamate antiporter could tie these pathological mechanisms together: its activity is enhanced by reactive oxygen species and inflammatory stimuli, and its enhancement might lead to the release of toxic amounts of glutamate, thereby triggering excitotoxicity and neurodegeneration.

Methods

Semi-quantitative Western blotting served to study protein expression of xCT, the specific subunit of system xc , as well as of regulators of xCT transcription, in the normal appearing white matter (NAWM) of MS patients and in the CNS and spleen of mice exposed to experimental autoimmune encephalomyelitis (EAE), an accepted mouse model of MS. We next compared the clinical course of the EAE disease, the extent of demyelination, the infiltration of immune cells and microglial activation in xCT-knockout (xCT−/−) mice and irradiated mice reconstituted in xCT−/− bone marrow (BM), to their proper wild type (xCT+/+) controls.

Results

xCT protein expression levels were upregulated in the NAWM of MS patients and in the brain, spinal cord, and spleen of EAE mice. The pathways involved in this upregulation in NAWM of MS patients remain unresolved. Compared to xCT+/+ mice, xCT−/− mice were equally susceptible to EAE, whereas mice transplanted with xCT−/− BM, and as such only exhibiting loss of xCT in their immune cells, were less susceptible to EAE. In none of the above-described conditions, demyelination, microglial activation, or infiltration of immune cells were affected.

Conclusions

Our findings demonstrate enhancement of xCT protein expression in MS pathology and suggest that system xc on immune cells invading the CNS participates to EAE. Since a total loss of system xc had no net beneficial effects, these results have important implications for targeting system xc for treatment of MS.
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Metadata
Title
Absence of system xc − on immune cells invading the central nervous system alleviates experimental autoimmune encephalitis
Authors
Ellen Merckx
Giulia Albertini
Magdalena Paterka
Cathy Jensen
Philipp Albrecht
Michael Dietrich
Joeri Van Liefferinge
Eduard Bentea
Lise Verbruggen
Thomas Demuyser
Lauren Deneyer
Jan Lewerenz
Geert van Loo
Jacques De Keyser
Hideyo Sato
Pamela Maher
Axel Methner
Ann Massie
Publication date
01-12-2017
Publisher
BioMed Central
Published in
Journal of Neuroinflammation / Issue 1/2017
Electronic ISSN: 1742-2094
DOI
https://doi.org/10.1186/s12974-016-0787-0

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