The Effects of Echinacea Extract on the Gene Expression of Monocytes and Monocyte-derived Dendritic Cells.
- Author:
Jun Eun PARK
1
;
Kang Duk CHOI
;
Sung Hwan KIM
;
Dae Hyun HAHM
;
Jong Jin SEO
Author Information
1. Department of Pediatrics, Ajou University School of Medicine, Suwon, Korea. pedpje@ajou.ac.kr
- Publication Type:Original Article
- Keywords:
Echinacea;
Monocyte;
Monocyte-derived dendritic cell;
cDNA microarray chip
- MeSH:
Carrier Proteins;
Centers for Disease Control and Prevention (U.S.);
Dendritic Cells*;
Echinacea*;
Electron Transport Complex IV;
Gene Expression*;
Granulocyte-Macrophage Colony-Stimulating Factor;
Humans;
Interferons;
Interleukin-4;
Mannose;
Mass Screening;
Monocytes*;
Oligonucleotide Array Sequence Analysis;
Phosphotransferases;
Plants;
Superoxide Dismutase;
Syndecans;
Syntenins
- From:Korean Journal of Pediatrics
2005;48(7):779-788
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Echinacea, a traditional plant medicine has been used as immune-stimulant. Recent studies have revealed that extract of Echinacea has immunostimulatory effects on human blood mononuclear cells. This study was designed for the purpose of screening the genes associated with immunologic effects of Echinacea on monocytes and dendritic cells using a cDNA microarray chip. METHODS: CD14+monocyte cells were cultured for one day with Echinacea extract (final concentration: 50 microgram/mL) in experiment 1, but were cultured without Echinacea in experiment 2. The gene expression of these cultured monocytes was analyzed using the cDNA microarray chip. Dendritic cells produced from CD14+monocyte were cultured for five days with GM-CSF and IL-4, and then cultured for one day with Echinacea in experiment 3, but were done without Echinacea in experiment 4. RESULTS: In experiments 1 and 2, there were 17 significantly expressed genes with average expression ratios above 2.5, including interferon gamma-inducible protein 30 (IFI 30), CDC (cell-division-cylcle)-like kinase 2 (CLK 2), syndecan binding protein (syntenin), superoxide dismutase 2, etc. In experiments 3 and 4, there were 24 gene, with significantly expressed genes were 24 genes, which were insulin-like growth factor 2 (somatomedin A), methyl-CpG binding domain protein 3, IFI 30, small inducible cytokine subfamily A, member 22, etc. The genes encoding CD44, IFI 30, mannose receptor C type 1 (MRC 1), chemokine receptor 7 (CCR 7), CLK 2, syntenin and cytochrome C oxidase subunit VIII were significantly expressed in both monocytes and dendritic cells cultured with Echinacea. CONCLUSION: This study employed a cDNA microarray chip to elicit the immune-associated gene profile; the expression was enhanced by Echinacea in CD14+monocytes and dendritic cells. Thus we laid the basis for the quantitative and functional analysis of genes induced by Echinacea in monocytes and monocyte-derived dendritic cells.
