Myelin oligodendrocyte glycoprotein (MOG35-55) induced experimental autoimmune encephalomyelitis (EAE) in C57BL/6 mice.

Bittner S, Afzali AM, Wiendl H, Meuth SG

Research article (journal) | Peer reviewed

Abstract

Multiple sclerosis is a chronic neuroinflammatory demyelinating disorder of the central nervous system with a strong neurodegenerative component. While the exact etiology of the disease is yet unclear, autoreactive T lymphocytes are thought to play a central role in its pathophysiology. MS therapy is only partially effective so far and research efforts continue to expand our knowledge on the pathophysiology of the disease and to develop novel treatment strategies. Experimental autoimmune encephalomyelitis (EAE) is the most common animal model for MS sharing many clinical and pathophysiological features. There is a broad diversity of EAE models which reflect different clinical, immunological and histological aspects of human MS. Actively-induced EAE in mice is the easiest inducible model with robust and replicable results. It is especially suited for investigating the effects of drugs or of particular genes by using transgenic mice challenged by autoimmune neuroinflammation. Therefore, mice are immunized with CNS homogenates or peptides of myelin proteins. Due to the low immunogenic potential of these peptides, strong adjuvants are used. EAE susceptibility and phenotype depends on the chosen antigen and rodent strain. C57BL/6 mice are the commonly used strain for transgenic mouse construction and respond among others to myelin oligodendrocyte glycoprotein (MOG). The immunogenic epitope MOG35-55 is suspended in complete Freund's adjuvant (CFA) prior to immunization and pertussis toxin is applied on the day of immunization and two days later. Mice develop a "classic" self-limited monophasic EAE with ascending flaccid paralysis within 9-14 days after immunization. Mice are evaluated daily using a clinical scoring system for 25-50 days. Special considerations for care taking of animals with EAE as well as potential applications and limitations of this model are discussed.

Details about the publication

JournalJournal of Visualized Experiments
Volume2014
Issue86
StatusPublished
Release year2014 (30/12/2014)
Language in which the publication is writtenEnglish
DOI10.3791/51275
Link to the full texthttp://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84930794287&origin=inward
KeywordsAnimal model; Autoimmunity; Central nervous system; EAE; Experimental autoimmune encephalomyelitis; Immunology; Issue 86; MS; Multiple sclerosis; Neuroinflammation; Pertussis

Authors from the University of Münster

Bittner, Stefan
Department for Neurology
Meuth, Sven
Department for Neurology
Wiendl, Heinz Siegfried
Department for Neurology