Monomethylfumarate reduces in vitro migration of mononuclear cells
Autor: | M. Döbert, H.-P. Hartung, B. C. Kieseier, Susann Pankratz, Heinz Wiendl, Thomas Dehmel, Verena I. Leussink |
---|---|
Rok vydání: | 2013 |
Předmět: |
Adult
Male Chemokine Multiple Sclerosis Time Factors NF-E2-Related Factor 2 Glutamate-Cysteine Ligase Dermatology Matrix metalloproteinase Blood–brain barrier Peripheral blood mononuclear cell Statistics Nonparametric Chemokine receptor Downregulation and upregulation Fumarates Antigens CD Cell Movement medicine NAD(P)H Dehydrogenase (Quinone) Humans biology Cell adhesion molecule Chemistry Maleates General Medicine Flow Cytometry In vitro Psychiatry and Mental health medicine.anatomical_structure Gene Expression Regulation Immunology biology.protein Leukocytes Mononuclear Female Neurology (clinical) Heme Oxygenase-1 Signal Transduction |
Zdroj: | Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 35(7) |
ISSN: | 1590-3478 |
Popis: | Migration of immunocompetent cells into the central nervous system represents a key event in the immunopathogenesis of multiple sclerosis (MS). Fumaric acid esters have recently been approved for patients with MS. Their mode of action is not fully understood so far. We analyzed the effect of monomethylfumarate (MMF), the immediate metabolite of dimethylfumarate, on migration of lymphocytes and macrophages. Peripheral blood mononuclear cells (PBMCs) were isolated from patients with MS and healthy donors. PBMCs were treated with MMF in vitro and their migratory capacity was studied in a Boyden chamber assay. In addition, expression of matrix metalloproteinases (MMPs), chemokine receptors, adhesion molecules, and molecules of the oxidative stress cascade was assessed. MMF decreased the migratory capacity of T lymphocytes, but not of macrophages. Lymphocytes as well as macrophages responded to MMF by the upregulation of oxidative stress molecules; however, no effect was seen on the expression of MMPs, chemokine receptors, and adhesion molecules. There was no difference in comparison with cells from healthy controls. MMF reduces the migratory activity of lymphocytes most likely by changing their activational state. This points to a potential novel mode of action differentiating this drug from other available immunotherapies. |
Databáze: | OpenAIRE |
Externí odkaz: |