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Malondialdehyde modification of myelin oligodendrocyte glycoprotein leads to increased immunogenicity and encephalitogenicity
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry, Analytical Chemistry.
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2007 (English)In: European Journal of Immunology, ISSN 0014-2980, E-ISSN 1521-4141, Vol. 37, no 7, 1986-1995 p.Article in journal (Refereed) Published
Abstract [en]

Self proteins may become autoantigenic through structural modification. We studied malondialdehydation of recombinant rat (rr) myelin oligodendrocyte glycoprotein (MOG), an autoantigen in multiple sclerosis. Malondialdehyde (MDA) modification changed protein weight and charge, the location of these adducts being mapped by Fourier transform ion cyclotron resonance. Molecular modelling revealed significant differences in the MDA-rrMOG three-dimensional structure. DBA/1 mice immunised with MDA-rrMOG developed greater proliferative responses and more severe experimental autoimmune encephalomyelitis than mice immunised with unmodified rrMOG. MDA-rrMOG was taken up more effectively by antigen-presenting cells (APC), at least partially through scavenger receptors. Exposure to MDA-rrMOG led to increased expression of IL-23, IL-12 and IL-12R, indicating a role not only for increased antigen uptake but also for activation of APC. We thus provide biochemical, structural, immunological and clinical data that suggest that the post-translationally modified form of this myelin autoantigen is a more relevant form of the molecule.

Place, publisher, year, edition, pages
2007. Vol. 37, no 7, 1986-1995 p.
Keyword [en]
Autoimmunity, EAE, Immune response, Oxidation, Post-translational modification
National Category
Medical and Health Sciences Natural Sciences
URN: urn:nbn:se:uu:diva-12356DOI: 10.1002/eji.200636912ISI: 000247828200029OAI: oai:DiVA.org:uu-12356DiVA: diva2:40125
Available from: 2007-12-14 Created: 2007-12-14 Last updated: 2011-01-31Bibliographically approved

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