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N-乙酰半胱氨酸对化学性缺氧引起HaCaT细胞损伤的保护作用 被引量:1

Protective effect of N-acetyl cysteine against chemical hypoxia-induced injury to an immortal human skin keratinocyte line HaCaT
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摘要 目的 探讨N-乙酰半胱氨酸(NAC)能否保护人皮肤永生化角质形成细胞(HaCaT)对抗化学性低氧模拟剂氯化钴(CoCl2)诱导的损伤及对炎症因子的影响.方法 用2000 μmol/L 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.应用CCK-8比色法检测细胞存活率;ELISA试剂盒检测细胞培养基中IL-6、IL-8和TNF-α的水平;罗丹明123(Rh123)染色/荣光显微镜照相术检测线粒体膜电位(MMP);谷胱甘肽试剂盒检测细胞内还原型谷胱甘肽(GSH)的含量.结果 不同浓度的NAC预处理HaCaT细胞2 h能明显对抗CoCl2引起的存活率降低;CoCl2处理HaCaT细胞4 h能使IL-6、IL-8和TNF-α的释放显著增加,GSH水平及MMP降低;2000μmol/L NAC预处理2 h能使IL-6和IL-8的释放显著减少,并能使细胞内GSH含量增多,MMP升高.结论 氧自由基清除剂NAC能对抗CoCl2诱导的HaCaT细胞损伤及炎症反应,此作用可能与其减轻细胞内的氧化应激反应有关. Objective To estimate the influences of N-acetyl cysteine (NAC) on a chemical hypoxiamimetic agent CoCl2 induced-injury to, and expressions of inflammatory factors by, an immortal human skin keratinocyte line HaCaT. Methods HaCaT cells were treated with CoCl2 of 2000 μmol/L for 4 hours to set up a chemical hypoxia-induced cell model of skin injury. NAC of various concentrations ( 1000, 2000, 3000 μmol/L)was used to pretreat HaCaT cells for 2 hours prior to the establishment of cell model. After these treatments,cell viability was detected by cell counting kit 8 (CCK-8), the levels of interleukin 6 and 8 (IL-6 and -8) and tumor necrosis factor α (TNF-α) in culture supernatant by ELISA kits, mitochondrial membrane potential (MMP) by rhodamine 123 (Rh123) staining and photofluorography, intracellular reduced glutathione (GSH)content by glutathione detection kit. Results An obvious decline was observed in HaCaT cell viability after pretreatment with various concentrations of NAC for 2 hours. The treatment with CoCl2 of 2000 μmol/L for 4 hours induced an elevation in the supernatant levels of IL-6, IL-8 and TNF-α and a decrease in GSH content and MMP, while the pretreatment with NAC for 2 hours retarded the CoCl2-induced increase in IL-6 and IL-8 levels as well as decrease in GSH content and MMP. Conclusion The reactive oxygen species (ROS) scavenger NAC can protect against CoCl2-induced injury to and inflammatory reaction in HaCaT cells, which may be associated with a decrement in oxidative stress.
出处 《中华皮肤科杂志》 CAS CSCD 北大核心 2010年第12期859-862,共4页 Chinese Journal of Dermatology
基金 广东省科技计划(2010B08071035)
关键词 自由基清除剂 缺氧 角蛋白细胞 炎症 Free radical scavengers Anoxia Keratinocytes Inflammation
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参考文献8

  • 1Galenko-Yaroshevskii VP,Bagmetova EN,Fil'chukova IA,et al.Antihypoxic and antinecrotic effect of mexidol in skin ischemia.Bull Exp Biol Med,2005,139(2):202-206.
  • 2李吉,李薇,谢红付,陈明亮,陈翔,朱武.UVA对成纤维细胞和HaCaT细胞形态及诱导型一氧化氮合酶产生水平的影响[J].中华皮肤科杂志,2007,40(11):680-683. 被引量:2
  • 3Xiao L,Kaneyasu K,Saitoh Y,et al.Cytoprotective effects of the lipoidic-liquiform pro-vitamin C tetra-isopalmitoyl-ascorbate (VC-IP)against ultraviolet-A ray-induced injuries in human skin cells together with collagen retention,MMP inhibition and p53 gene repression.J Cell Biochem,2009,106(4):589-598.
  • 4Galenko-Yaroshevskii VP,Agadzhanova AV,Lapina NV,et al.Effectiveness of combined treatment with superoxide dismutase and Reamberin during skin ischemia.Bull Exp Biol Med,2006,142(6):707-709.
  • 5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.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[J].中国药理学通报,2010,26(5):633-637. 被引量:4
  • 6Chen SL,Yang CT,Yang ZL,et al.Hydrogen sulphide protects H9c2 cells against chemical hypoxia-induced injury.Clin Exp Pharmacol Physiol,2010,37(3):316-321.
  • 7Zou W,Yan M,Xu W,et al.Cobalt chloride induces PC12 cells apoptosis through reactive oxygen species and accompanied by AP-1 activation.J Neurosci Res,2001,64(6):646-653.
  • 8Jung JY,Kim WJ.Involvement of mitochondrial-and Fas-mediated dual mechanism in CoCl2-induced apoptosis of rat PC12 cells.Neurosci Lett,2004,371(2-3):85-90.

二级参考文献25

  • 1陈明亮,李吉,肖伟荣,孙磊,唐桦,王琳,吴凌燕,陈翔,谢红付.白藜芦醇对UVA致HaCaT细胞氧化损伤的保护作用(英文)[J].中南大学学报(医学版),2006,31(5):635-639. 被引量:7
  • 2Jung J Y,Mo H C,Yang K H,et al.Inhibition by epigallocatechin gallate of CoCl2-induced apoptosis in rat PC12 cells[J].Life Sci,2007,80(15):1355-63.
  • 3Kim K S,Rajagopal V,Gonsalves C,et al.A novel role of hypoxia-inducible factor in cobalt chloride-and hypoxia-mediated expression of IL-8 chemokine in human endothelial cells[J].J Immunol,2006,177 (10):7211-24.
  • 4Schmalz G,Schweikl H,Hiller K A.Release of prostaglandin E2,IL-6 and IL-8 from human oral epithelial culture models after exposure to compounds of dental materials[J].Eur J Oral Sci,2000,108(5):442-8.
  • 5Ermolli M,Menne C,Pozzi G,et al.Nickel,cobalt and chromium-induced cytotoxicity and intracellular accumulation in human hacat keratinocytes[J].Toxicology,2001,159(1-2):23-31.
  • 6Amersi F,Buelow R,Kato H,et al.Upregulation of heme oxygenase-1 protects genetically fat Zucker rat livers from ischemia/reperfusion injury[J].J Clin Invest,1999,104(11):1631-9.
  • 7Loboda A,Jazwa A,Wegiel B,et al.Heme oxygenase-1-dependent and -independent regulation of angiogenic genes expression:effect of cobalt protoporphyrin and cobalt chloride on VEGF and IL-8 synthesis in human microvascular endothelial cells[J].Cell Mol Biol (Noisy-le-grand),2005,51(4):347-55.
  • 8Dongari-Bagtzoglou A I,Ebersole J L.Increased presence of interleukin-6 (IL-6) and IL-8 secreting fibroblast subpopulations in adult periodontitis[J].J Periodontol,1998,69(8):899-910.
  • 9Murakami S,Hino E,Shimabukuro Y,et al.Direct interaction between gingival fibroblasts and lymphoid cells induces inflammatory cytokine mRNA expression in gingival fibroblasts[J].J Dent Res,1999,78 (1):69-76.
  • 10Gemmell E,Marshall R I,Seymour G J.Cytokines and prostaglandins in immune homeostasis and tissue destruction in periodontal disease[J].Periodontol 2000,1997,14:112-43.

共引文献4

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  • 1Barcelos LS,Duplaa C,Kr(a)nkel N,et al.Human CD133+ progenitor cells promote the healing of diabetic ischemic ulcers by paracrine stimulation of angiogenesis and activation of Wnt signaling.Circ Res,2009,104(9):1095-1102.
  • 2Hayden MS,Ghosh S.Signaling to NF-kappaB.Genes Dev,2004,18(18):2195-2224.
  • 3Li Q,Verma IM.NF-kappaB regulation in the immune system.Nat Rev Immunol,2002,2(10):725-734.
  • 4Venkatachalam K,Prabhu SD,Reddy VS,et al.Neutralization of interleukin-18 ameliorates ischemia/reperfusion-induced myocardial injury.J Biol Chem,2009,284(12):7853-7865.
  • 5Cheng O,Ostrowski RP,Liu W,et al.Activation of liver X receptor reduces global ischemic brain injury by reduction of nuclear factor-kappaB.Neuroscience,2010,166(4):1101-1109.
  • 6Sultana C,Shen Y,Johnson C,et al.Cobalt chloride-induced signaling in endothelium leading to the augmented adherence of sickle red blood cells and transendothelial migration of monocyte-like HL-60 cells is blocked by PAF-receptor antagonist.J Cell Physiol,1999,179(1):67-78.
  • 7Saliou C,Kitazawa M,McLaughlin L,et al.Antioxidants modulate acute solar ultraviolet radiation-induced NF-kappa-B activation in a human keratinocyte cell line.Free Radic Biol Med,1999,26(1-2):174-183.
  • 8Lim JH,Lee JC,Lee YH,et al.Simvastatin prevents oxygen and glucose deprivation/reoxygenation-induced death of cortical neurons by reducing the production and toxicity of 4-hydroxy-2E-nonenal.J Neurochem,2006,97(1):140-150.
  • 9Liu Y,Zhang XJ,Yang CH,et al.Oxymatrine protects rat brains against permanent focal ischemia and downregulates NF-kappaB expression.Brain Res,2009,1268:174-180.
  • 10Pieper GM,Olds C,Hilton G,et al.Antioxidant treatment inhibits activation of myocardial nuclear factor kappa B and inhibits nitrosylation of myocardial heme protein in cardiac transplant rejection.Antioxid Redox Signal,2001,3(1):81-88.

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