20S-dihydroprotopanaxadiol, a ginsenoside derivative, boosts innate immune responses of monocytes and macrophages.

PISSN
1226-8453
Publication Dbxref
PMID:24198654
Title
20S-dihydroprotopanaxadiol, a ginsenoside derivative, boosts innate immune responses of monocytes and macrophages.
Publication Type
Journal Article
Series Name
Journal of ginseng research
Volume
37
Publication Year
2013
Issue
3
Page Numbers
293-9
DOI
10.5142/jgr.2013.37.293
Journal Abbreviation
J Ginseng Res
Publication Date
2013 Jul
Unique Local Identifier

Kim MY, Cho JY. 20S-dihydroprotopanaxadiol, a ginsenoside derivative, boosts innate immune responses of monocytes and macrophages.. Journal of ginseng research. 2013 Jul; 37(3):293-9.

Citation
Kim MY, Cho JY. 20S-dihydroprotopanaxadiol, a ginsenoside derivative, boosts innate immune responses of monocytes and macrophages.. Journal of ginseng research. 2013 Jul; 37(3):293-9.
ISSN
1226-8453
Language Abbr
eng
Publication Model
Print
Authors
Kim MY, Cho JY
Language
English
Elocation
10.5142/jgr.2013.37.293
Journal Country
Korea (South)
Abstract

20S-dihydroprotopanaxadiol (2H-PPD) is a derivative of protopanaxadiol, a glycone of ginsenosides prepared from Panax ginseng. Although ginsenosides and acidic polysaccharides are known to be major active ingredients in ginseng, the immunopharmacological activities of their metabolites and derivatives have not been fully explored. In this study, we aimed to elucidate the regulatory action of 2H-PPD on the function of monocytes and macrophages in innate immune responses. 2H-PPD was able to boost the phagocytic uptake of fluorescein isothiocyanate-dextran in macrophages and enhance the generation of radicals (reactive oxygen species) in sodium nitroprusside-treated RAW264.7 cells. The surface levels of the costimulatory molecules such as CD80 and CD86 were also increased during 2H-PPD treatment. In addition, this compound boosted U937 cellcell aggregation induced by CD29 and CD43 antibodies, but not by cell-extracellular matrix (fibronectin) adhesion. Similarly, the surface levels of CD29 and CD43 were increased by 2H-PPD exposure. Therefore, our results strongly suggest that 2H-PPD has the pharmacological capability to upregulate the functional role of macrophages/monocytes in innate immunity.

Database Reference Annotations
Is Obsolete
False