6533b81ffe1ef96bd127856e
RESEARCH PRODUCT
Primary oligodendrocyte death does not elicit anti-CNS immunity.
Thorsten BuchThorsten BuchClaudia BühlmannGiuseppe LocatelliBettina SobottkaMartin KrügerBarbara IngoldIngo BechmannAri WaismanBurkhard BecherFrank L. HeppnerFriederike FrommerSimone WörtgeKhalad Karramsubject
Encephalomyelitis Autoimmune ExperimentalMultiple SclerosisEncephalomyelitisTransgene610 Medicine & healthMice TransgenicBiology10263 Institute of Experimental Immunology03 medical and health sciencesMyelinMice0302 clinical medicineAntigenImmunitymedicineAnimalsGene Knock-In TechniquesCells Cultured030304 developmental biology0303 health sciencesCell DeathGeneral NeuroscienceMultiple sclerosis2800 General Neurosciencemedicine.diseaseOligodendrocyteOligodendrogliamedicine.anatomical_structureImmunology570 Life sciences; biologyExperimental pathologyNeuroscience030217 neurology & neurosurgerydescription
Anti-myelin immunity is commonly thought to drive multiple sclerosis, yet the initial trigger of this autoreactivity remains elusive. One of the proposed factors for initiating this disease is the primary death of oligodendrocytes. To specifically test such oligodendrocyte death as a trigger for anti-CNS immunity, we inducibly killed oligodendrocytes in an in vivo mouse model. Strong microglia-macrophage activation followed oligodendrocyte death, and myelin components in draining lymph nodes made CNS antigens available to lymphocytes. However, even conditions favoring autoimmunity-bystander activation, removal of regulatory T cells, presence of myelin-reactive T cells and application of demyelinating antibodies-did not result in the development of CNS inflammation after oligodendrocyte death. In addition, this lack of reactivity was not mediated by enhanced myelin-specific tolerance. Thus, in contrast with previously reported impairments of oligodendrocyte physiology, diffuse oligodendrocyte death alone or in conjunction with immune activation does not trigger anti-CNS immunity.
year | journal | country | edition | language |
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2012-01-01 | Nature neuroscience |