Effect of puerarin on the release of interleukin-8 in co-culture of human bronchial epithelial cells and neutrophils.
- Author:
Wei PANG
1
;
Xiao-Mei LAN
;
Cheng-Bin WANG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Bronchi; cytology; Cell Communication; drug effects; Cell Line; Coculture Techniques; Epithelial Cells; cytology; drug effects; metabolism; Fluorescence; Gene Expression Regulation; drug effects; Humans; Interleukin-8; genetics; secretion; Isoflavones; pharmacology; Neutrophils; cytology; drug effects; metabolism; RNA, Messenger; genetics; metabolism; Real-Time Polymerase Chain Reaction
- From: Chinese journal of integrative medicine 2012;18(4):283-287
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo investigate the effect of puerarin on interleukin (IL)-8 mRNA expression and the protein release in the co-culture of human bronchial epithelial (BEAS-2B) cells and human neutrophils.
METHODSBEAS-2B cells and neutrophills were cultured separately and co-cultured with puerarin (50, 100, and 200 μg/mL) for a predetermined time. Cytokines in culture supernatant were evaluated by protein array and IL-8 quantified by enzyme-linked immunosorbent assay (ELISA). IL-8 mRNA expression was evaluated by real-time quantitative polymerase chain reaction (real-time qPCR).
RESULTSThe co-culture of BEAS-2B cells and neutrophils exhibited synergistic effects on IL-8 mRNA expression in BEAS-2B cells, but not in neutrophils after 12 h incubation (P<0.01), as compared with that in BEAS-2B cells or neutrophils alone. IL-8 protein release in the culture supernatant was obviously elevated when BEAS-2B cells were co-cultured with human neutrophils as compared with that in the supernatant of BEAS-2B cells or neutrophils alone after incubated for 2, 6, 12, and 18 h (P<0.01). Treatment with puerarin could significantly down-regulate the expression of IL-8 mRNA in BEAS-2B cells and IL-8 release in the supernatant of the co-culture of BEAS-2B cells and neutrophils (P<0.01).
CONCLUSIONPuerarin could exhibit anti-inflammatory activity by suppressing IL-8 production from the co-culture of human bronchial epithelial cells and neutrophils.