Inflammatory cytokine and microRNA responses of primary human dendritic cells cultured with Helicobacter pylori strains

被引:30
作者
de la Guardia, Anais Hoces [1 ,2 ]
Staedel, Cathy [3 ,4 ]
Kaafarany, Itidal [1 ,2 ]
Clement, Aurelien [1 ,2 ]
Baudron, Claire Roubaud [1 ,2 ,5 ]
Megraud, Francis [1 ,2 ]
Lehours, Philippe [1 ,2 ]
机构
[1] Univ Bordeaux, Bacteriol Lab, Bordeaux, France
[2] INSERM, U853, Bordeaux, France
[3] Univ Bordeaux, ARNA Lab, Bordeaux, France
[4] INSERM, U869, Bordeaux, France
[5] CHU Bordeaux, Pole Gerontol Clin, Bordeaux, France
来源
FRONTIERS IN MICROBIOLOGY | 2013年 / 4卷
关键词
Helicobacter pylori; dendritic cell; inflammation; TNF alpha; microRNA; SIGNALING PATHWAY; VIRULENCE FACTORS; MIR-155; ACTIVATION; INDUCTION; INFECTION; MACROPHAGES; EXPRESSION; MATURATION; LYMPHOMA;
D O I
10.3389/fmicb.2013.00236
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Primary human dendritic cells (DC) were used to explore the inflammatory effectors, including cytokines and microRNAs, regulated by Helicobacter pylon. In a 48 h ex-vivo co-culture system, both H. pylon B38 and B45 strains activated human DCs and promoted a strong inflammatory response characterized by the early production of pro-inflammatory INFot and IL-6 cytokines, followed by IL-10, IL-113, and IL-23 secretion. IL-23 was the only cytokine dependent on the cag pathogenicity island status of the bacterial strains. DC activation and cytokine production were accompanied by an early miR-146a upregulation followed by a strong miR-155 induction, which mainly controlled INFot production. These results pave the way for further investigations into the nature of H. pylon antigens and the subsequently activated signaling pathways involved in the inflammatory response to H. pylon infection, the deregulation of which may likely contribute to gastric lymphomagenesis.
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页数:13
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