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脂多糖对人鼻黏膜上皮细胞人β防御素2诱导表达的影响 被引量:1

Roles of lipopolysaccharide in the expression of human β defensin 2 in human nasal mucosa epithelial cells
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摘要 目的观察脂多糖(LPS)诱导人鼻黏膜上皮细胞人β防御素2(h BD-2)表达的影响。方法用LPS刺激人鼻黏膜上皮细胞,反转录聚合酶链反应(RT-PCR)检测h BD-2 mRNA的表达,免疫细胞化学检测h BD-2蛋白的表达。结果 LPS刺激2 h后人鼻黏膜上皮细胞可见h BD-2 mRNA的表达,并呈剂量和时间依赖性;刺激4 h后人鼻黏膜上皮细胞胞质中可见h BD-2蛋白的表达。结论一定剂量的LPS可诱导人鼻黏膜上皮细胞h BD-2的表达,这种表达具有一定的剂量和时间依赖性。 Objective To explore the role of lipopolysaceharide (LPS) in the expression of human β defensin 2 (hBD-2) in human nasal mucosa epithelial cells. Methods After the human nasal mucosa epithelial cells were stimulated with LPS, the expression of hBD-2 mRNA was detected by reverse transcription polymerase chain reaction (RT-PCR) and the expression of hBD-2 protein was deteeted by immunoeytochemistry. Results The hBD-2 mRNA could be detected 2 hours after LPS stimulation and expressed in a dose- and time-dependent manner. The hBD-2 protein could be detected in cytoplasm 4 hours after LPS stimulation. Conclusions A certain dose of LPS could induce the expression of hBD-2 in human nasal mueosa epithelial cells in a dose- and time-dependent manner.
作者 胡秀娟 刘海兵 贺广湘 HU Xiu-juan LIU Hai-bing HE Guang-xiang(Department of Otolaryngology Head and Neck Surgery, the Affiliated Hospital of Chengdu University, Chengdu 610081, China)
出处 《中国眼耳鼻喉科杂志》 2017年第4期245-248,共4页 Chinese Journal of Ophthalmology and Otorhinolaryngology
基金 湖南省自然科学基金项目(14JJ2038) 湖南省长沙市科技项目(K1203050-31)
关键词 人鼻黏膜上皮细胞 人Β防御素2 脂多糖 Human nasal mucosa epithelial cells Human β defensin 2 Lipopolysaccharide
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  • 1Kumar S, Boehm J, Lee J C. p38 MAP kinases., key signalling molecules as therapeutic targets for inflammatory diseases. Nat Rev Drug Discov, 2003, 2:717-726.
  • 2Lewis A J,Manning A M. New targets for anti-inflammatory drugs. Curr Opin Chem Biol, 1999,3:489--494.
  • 3Hamilton L M, Davies D E, Wilson S J, et al, The bronchial epithelium in asthma-much more than a passive barrier, Monaldi Arch Chest Dis, 2001, 56; 48-54.
  • 4Newton R, Holden N. Inhibitors of p38 mitogen-aetivated protein kinase: potential as anti-inflammatory agents in asthma? Bio Drugs, 2003,17 : 113-129.
  • 5Yamaya M, Finkbeiner W E, Chun S Y,et al. Differentiated structure and function of cultures from human tracheal epithelium. Am J Physiol, 1992, 262: 713-724.
  • 6Han J, Lee J D, Bibbs L,et al. A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells.Science, 1994, 265: 808-811.
  • 7Dean J L, Brook M, Clark A R, et al. p38 mitogen-aetivated protein kinase regulates cyclooxygenase-2 mR-NA stability and transcription in ipopolysaccharidetreated human monocytes. J Biol Chem, 1999,274:264-269.
  • 8Masuda A, Yoshikai Y, Aiba K. Th2 cytokine production from mast cells is directly induced by lipopolysaccharide and distinctly regulated by c-Jun N-terminal kinase and p38 pathways. J Immunol, 2002,169 : 3801-3810.
  • 9Schwartz D A. The role of TLR4 in endotoxin responsiveness in humans. J Endotoxin Res, 2001,7: 389-393.
  • 10Lee J C, Kassis S, Kumar S. p38Mitogen-activated protein kinase inhibitors mechanisms and therapeutic potentials. Pharmacol Ther, 1999,82 : 389-397.

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