www.uhasselt.be
DSpace

Document Server@UHasselt >
Research >
All items >

Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/13936

Title: Myelin-Derived Lipids Modulate Macrophage Activity by Liver X Receptor Activation
Authors: Bogie, J.
Timmermans, S.
Huynh-Thu, V.
Irrthum, A.
Smeets, H.J.M.
Gustafsson, J.A.
Steffensen, K.R.
Mulder, M.T.
Stinissen, P.
Hellings, N.
Hendriks, J. J. A.
Issue Date: 2012
Citation: PLoS One
Abstract: Multiple sclerosis is a chronic, inflammatory, demyelinating disease of the central nervous system in which macrophages and microglia play a central role. Foamy macrophages and microglia, containing degenerated myelin, are abundantly found in active multiple sclerosis lesions. Recent studies have described an altered macrophage phenotype after myelin internalization. However, it is unclear by which mechanisms myelin affects the phenotype of macrophages and how this phenotype can influence lesion progression. Here we demonstrate, by using genome wide gene expression analysis, that myelin-phagocytosing macrophages have an enhanced expression of genes involved in migration, phagocytosis and inflammation. Interestingly, myelin internalization also induced the expression of genes involved in liver-X-receptor signalling and cholesterol efflux. In vitro validation shows that myelin-phagocytosing macrophages indeed have an increased capacity to dispose intracellular cholesterol. In addition, myelin suppresses the secretion of the pro-inflammatory mediator IL-6 by macrophages, which was mediated by activation of liver-X-receptor β. Our data show that myelin modulates the phenotype of macrophages by nuclear receptor activation, which may subsequently affect lesion progression in demyelinating diseases such as multiple sclerosis.
URI: http://hdl.handle.net/1942/13936
ISI #: 000308738500104
ISSN: 1932-6203
Category: A1
Type: Journal Contribution
Validation: ecoom, 2013
Appears in Collections: Biomedical Research Institute
Immunology - Biochemistry

Files in This Item:

There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.