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Dimethylfumarate induces apoptosis in human mast cells
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4507405
Author(s) Förster, Anja; Preussner, Liane M.; Seeger, Jens M.; Rabenhorst, Anja; Kashkar, Hamid; Mrowietz, Ulrich; Hartmann, Karin
Author(s) at UniBasel Hartmann, Karin
Year 2013
Title Dimethylfumarate induces apoptosis in human mast cells
Journal Experimental Dermatology
Volume 22
Number 11
Pages / Article-Number 719-24
Mesh terms Apoptosis, drug effects; Calcium, chemistry; Caspase 6, metabolism; Caspase 9, metabolism; Cell Death; Cell Line; Dermatologic Agents, chemistry; Dexamethasone, chemistry; Dimethyl Fumarate; Etoposide, chemistry; Fumarates, chemistry; Humans; Interleukin-8, metabolism; Maleates, chemistry; Mast Cells, drug effects; Methotrexate, chemistry; Psoriasis, pathology; TNF-Related Apoptosis-Inducing Ligand, chemistry; bcl-2 Homologous Antagonist-Killer Protein, metabolism; bcl-2-Associated X Protein, metabolism
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.
Publisher Wiley
ISSN/ISBN 0906-6705 ; 1600-0625
edoc-URL https://edoc.unibas.ch/70779/
Full Text on edoc No
Digital Object Identifier DOI 10.1111/exd.12247
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/24112621
ISI-Number WOS:000330102500007
Document type (ISI) Journal Article
 
   

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02/05/2024