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Dimethylfumarate induces apoptosis in human mast cells
Authors:Anja Förster  Liane M. Preussner  Jens M. Seeger  Anja Rabenhorst  Hamid Kashkar  Ulrich Mrowietz  Karin Hartmann
Affiliation:1. Department of Dermatology, University of Cologne, , Cologne, Germany;2. Miltenyi Biotec GmbH, , Bergisch Gladbach, Germany;3. Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, , Cologne, Germany;4. Center for Molecular Medicine (CMMC), University of Cologne, , Cologne, Germany;5. Psoriasis Center, Department of Dermatology, University Medical Center Schleswig‐Holstein, Campus Kiel, , Kiel, Germany
Abstract:
Mast cells modulate autoimmune diseases such as psoriasis and multiple sclerosis. Fumaric acid esters (FAEs) are widely used for the treatment of psoriasis, and dimethylfumarate (DMF) has recently been approved for multiple sclerosis. In this study, we analysed the cytotoxic effect of FAEs on human mast cells. Specifically, cell death was analysed in the human mast cell line HMC‐1 and in primary cord blood‐derived mast cells (CBMCs) after incubation with fumaric acid (FA), monomethylfumarate (MMF), DMF and calcium bis(monomethylfumarate) (Ca‐MF). Our data show that only DMF potently induces apoptotic cell death in HMC‐1 cells and CBMCs. DMF‐mediated apoptosis was associated with increased expression of Bax and Bak and activation of caspase‐9 and caspase‐6. Interestingly, DMF also enhanced the sensitivity of CBMCs towards TRAIL‐ and dexamethasone‐induced apoptosis. These findings demonstrate for the first time that DMF induces apoptosis of human mast cells, primarily via the mitochondrial apoptotic pathway. Our study contributes to the understanding of the beneficial effects of FAEs in autoimmune diseases and provides a rationale for exploiting FAEs for other diseases associated with mast cells.
Keywords:apoptosis  dimethylfumarate  fumaric acid esters  mast cells  psoriasis
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