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Fucoidan prevents C epsilon germline transcription and NFkappaB p52 translocation for IgE production in B cells.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2006 Nov 24; Vol. 350 (3), pp. 501-7. Date of Electronic Publication: 2006 Aug 10. - Publication Year :
- 2006
-
Abstract
- Fucoidan, a dietary fiber contained in seaweed, reduces the increase of antigen-specific IgE in mice exposed to ovalbumin. In this study, we investigated the effect of fucoidan on IgE production and intracellular events in B cells in vitro. Fucoidan inhibited the production of IgE and C epsilon germline transcription in murine B cells induced by IL-4 (100 ng/ml) and anti-CD40 antibodies (10 microg/ml), whereas it stimulated cell proliferation. A significant effect of fucoidan on IgE production was observed when B cells were stimulated with a higher dose (5 microg/ml) of anti-CD40 antibodies, but not when stimulated with lower doses (1.25, 2.5 microg/ml), regardless of the IL-4 concentrations. Moreover, nuclear translocation of NFkappaB p52, but neither that of NFkappaB p65, nor the phosphorylation of JAK1 and STAT6 was reduced by fucoidan. These results suggest that fucoidan inhibited IgE production by preventing the NFkappaB p52-mediated pathways activated by CD40.
- Subjects :
- Animals
B-Lymphocytes drug effects
Cells, Cultured
Dose-Response Relationship, Drug
Male
Mice
Mice, Inbred C57BL
Micronucleus, Germline metabolism
Signal Transduction drug effects
Signal Transduction physiology
B-Lymphocytes metabolism
CD40 Antigens metabolism
Immunoglobulin E metabolism
NF-kappa B p52 Subunit metabolism
Polysaccharides administration & dosage
Protein Kinase C-epsilon metabolism
Transcription, Genetic drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 350
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 17027924
- Full Text :
- https://doi.org/10.1016/j.bbrc.2006.08.009