Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3063809 | Journal of Neuroimmunology | 2016 | 7 Pages |
•Laquinimod can activate the transcription factor Aryl hydrocarbon receptor.•Aryl hydrocarbon receptor functionality is essential for laquinimods efficacy in EAE.•Laquinimod elevates BDNF expression in the CNS, associated with neuroprotection.
Though several functional properties of laquinimod have been identified, our understanding of the underlying mechanisms is still incomplete. Since the compound elicits similar immunomodulatory effects to ligands of the aryl hydrocarbon receptor (AhR), we compared the efficacy of laquinimod in experimental autoimmune encephalomyelitis (EAE)-afflicted wild-type and AhR-deficient mice. Laquinimod failed to ameliorate clinical symptoms and leukocyte infiltration in AhR-deficient mice; however, treatment exerted neuroprotection by elevation of brain-derived neurotrophic factor (BDNF) independent of genetic profile. Thus, our data identify the AhR pathway in these mutant mice as crucial for the immunomodulatory, but not neuroprotective, efficacy of laquinimod in EAE.
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