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化学性低氧模拟剂氯化钴诱导人角质形成细胞炎症反应的研究

Study on chemical hypoxia-mimetic (CoCl2) agent-induced inflammatory reaction in human keratinocytes

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【作者】 林春喜张美芬杨春涛杨战利凌宏忠孟金兰曾凡钦陈培熹冯鉴强

【Author】 LIN Chun-xi1,ZHANG Mei-fen2,YANG Chun-tao3,YANG Zhan-li3,LING Hong-zhong4,MENG Jin-lan3,ZENG Fan-qin5,CHEN Pei-xi3,FENG Jian-qiang3(1.Dep of Intensive Care of Cardiovasology,the First Affiliated Hospital,2.School of Nursing,3.Dep of Physiology,Zhongshan School of Medicine,4.Dep of Dermatology,the First Affiliated Hospital,5.Dep of Dermatology,the Second Affiliated Hospital,Sun Yat-sen University,Guangzhou 510080,China)

【机构】 中山大学附属第一医院CCU科中山大学护理学院中山大学中山医学院生理学教研室中山大学附属第一医院皮肤科中山大学附属第二医院皮肤科

【摘要】 目的探讨化学性低氧模拟剂氯化钴对人皮肤角质形成细胞(HaCat)炎症反应的影响。方法用不同浓度的CoCl2处理HaCat细胞,建立化学性低氧诱导皮肤细胞损伤的实验模型后,检测细胞存活率、细胞内活性氧(ROS)、线粒体膜电位(MMP)、细胞培养液中白介素6(IL-6)和白介素8(IL-8)水平以及血红素加氧酶(HO-1)表达。结果在500~3000μmol.L-1浓度范围内,CoCl2可降低HaCat细胞存活率,且CoCl2剂量越大、细胞存活率降低越明显;2000μmol.L-1CoCl2能诱导HaCat细胞产生氧化应激反应,使胞内ROS生成增多,MMP降低;CoCl2能诱导HaCat细胞产生炎症反应,使IL-6和IL-8释放增多;1000~3000μmol.L-1CoCl2能上调HO-1的表达。结论CoCl2在诱导HaCat细胞产生氧化应激反应的同时,也能引起炎症反应,促进IL-6和IL-8的释放及HO-1表达上调。

【Abstract】 Aim To explore the effect of chemical hypoxia-mimetic agent,cobalt chloride(CoCl2)on inflammatory reaction in human keratinocytes(HaCat cells).Methods After HaCat cells were treated with CoCl2 at different concentrations to set up a chemical hypoxia-induced cell model of skin injury,cell viability,intracellular reactive oxygen species(ROS),mitochondrial membrane potential(MMP),the levels of both interleukin 6(IL-6)and interleukin 8(IL-8)as well as the expression of heme oxygenase-1(HO-1)were detected.Results The viability of HaCat cells was reduced by CoCl2 at the concentrations from 500 to 3 000 μmol·L-1,and the higher CoCl2 doses,the lower cell viability was.CoCl2 induced oxidative stress reaction(increasing ROS production and decreasing MMP).CoCl2 induced inflammatory reaction,enhancing the release of IL-6 and IL-8.CoCl2 at concentrations from 1 000 to 3 000 μmol·L-1 upregulated HO-1 expression in HaCat cells.Conclusion CoCl2 induces not only oxidative stress,but also inflammatory reaction,increasing the release of both IL-6 and IL-8,as well as HO-1 expression.

【基金】 广东省科技计划资助项目(No2008B080703053)
  • 【文献出处】 中国药理学通报 ,Chinese Pharmacological Bulletin , 编辑部邮箱 ,2010年05期
  • 【分类号】R751
  • 【被引频次】4
  • 【下载频次】281
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