Sulforaphane Enhances MHC Class II-Restricted Presentation of Exogenous Antigens

Sulforaphane is an isothiocyanate found in cruciferous vegetables that has been reported to be an effective cancer preventive agent inducing growth arrest and/or cell death in cancer cells of various organs. This paper reports that sulforaphane exerts immunomodulatory activity on the MHC-restricted...

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Veröffentlicht in:Biomolecules & therapeutics 2011, 19(1), , pp.77-83
Hauptverfasser: Shin, Seul-Mee, Jung, Ki-Sung, Park, Yoon-Hee, Ko, Young-Wook, Lee, Chong-Kil, Cho, Kyung-Hae, Ha, Nam-Joo, Kim, Kyung-Jae
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Sprache:eng
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Zusammenfassung:Sulforaphane is an isothiocyanate found in cruciferous vegetables that has been reported to be an effective cancer preventive agent inducing growth arrest and/or cell death in cancer cells of various organs. This paper reports that sulforaphane exerts immunomodulatory activity on the MHC-restricted antigen presenting function. Sulforaphane effi ciently increased the class II-restricted presentation of an exogenous antigen, ovalbumin (OVA), in both dendritic cells (DCs) and peritoneal macrophages in vitro. The class II-restricted OVA presentation-enhancing activity of sulforaphane was also confi rmed using mice that had been injected with sulforaphane followed by soluble OVA. On the other hand, sulforaphane did not affect the class I-restricted presentation of exogenous OVA at concentrations that increase the class II-restricted antigen presentation. At a high concentration (20 μM),sulforaphane inhibited the class I-restricted presentation of exogenous OVA. Sulforaphane did not affect the phagocytic activity of the DCs, and the cell surface expression of total H-2K^b, B7-1, B7-2 and CD54 molecules, even though it increased the expression of I-A^b molecules to a barely discernable level. These results show that sulforaphane increases the class II-restricted antigen presenting function preferentially, and might provide a novel insight into the mechanisms of the anti-cancer effects of sulforaphane KCI Citation Count: 3
ISSN:1976-9148
2005-4483
DOI:10.4062/biomolther.2011.19.1.077