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1.
Chinese journal of integrative medicine ; (12): 360-368, 2014.
Article in English | WPRIM | ID: wpr-267202

ABSTRACT

<p><b>OBJECTIVE</b>In this study, we aimed to investigate the expressions of adhesion molecules on human bronchial epithelial cells and neutrophils in co-culture system, assess the effects of puerarin on suppressing these adhesion molecules expressions, and explore the roles of two crucial signal-transduction elements p38 mitogen-activated protein kinase (p38 MAPK) and nuclear factor kappa B (NF-κB) in modulating adhesion molecules expressions.</p><p><b>METHODS</b>Neutrophils and BEAS-2B cells (one human bronchial epithelial cell line) were co-cultured, and adhesion molecules expressions on cell surface were detected using flow cytometry. The mRNA levels of adhesion molecules were assessed by real-time quantitative polymerase chain reaction (real-time qPCR). Phosphorylated p38 MAPK and inhibitor κB were analyzed by Western blot.</p><p><b>RESULTS</b>In co-culture system, adhesion molecules expressions on BEAS-2B cells and neutrophils were enhanced significantly (P<0.05). Correspondingly, the mRNA levels of adhesion molecules were also increased greatly. Moreover, the pretreatment of peurarin obviously suppressed adhesion molecules expressions on cell surface. Furthermore, phosphorylated p38 MAPK and inhibitor κB in BEAS-2B cells and neutrophils were elevated in co-culture system, but decreased significantly after upon the treatment of peurarin (P<0.05).</p><p><b>CONCLUSIONS</b>Coculture boosted the interactions between human bronchial epithelial cells and neutrophils mimicking airway inflflammation, whereas peurarin decreased the expression of adhesion molecules on cell surface by suppressing the activities of p38 MAPK and NF-κB pathways, and exhibiting its anti-inflflammation activity.</p>


Subject(s)
Animals , Cattle , Base Sequence , Bronchi , Cell Biology , Metabolism , Cell Adhesion Molecules , Metabolism , Cell Line , Coculture Techniques , DNA Primers , Down-Regulation , Epithelial Cells , Metabolism , Isoflavones , Pharmacology , NF-kappa B , Metabolism , Neutrophils , Metabolism , Phosphorylation , Real-Time Polymerase Chain Reaction , p38 Mitogen-Activated Protein Kinases , Metabolism
2.
Chinese journal of integrative medicine ; (12): 283-287, 2012.
Article in English | WPRIM | ID: wpr-289669

ABSTRACT

<p><b>OBJECTIVE</b>To 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.</p><p><b>METHODS</b>BEAS-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).</p><p><b>RESULTS</b>The 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).</p><p><b>CONCLUSION</b>Puerarin could exhibit anti-inflammatory activity by suppressing IL-8 production from the co-culture of human bronchial epithelial cells and neutrophils.</p>


Subject(s)
Adult , Humans , Bronchi , Cell Biology , Cell Communication , Cell Line , Coculture Techniques , Epithelial Cells , Cell Biology , Metabolism , Fluorescence , Gene Expression Regulation , Interleukin-8 , Genetics , Bodily Secretions , Isoflavones , Pharmacology , Neutrophils , Cell Biology , Metabolism , RNA, Messenger , Genetics , Metabolism , Real-Time Polymerase Chain Reaction
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