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脂多糖刺激对小鼠腹腔巨噬细胞HMGB1表达的影响 被引量:1

Effect of Stimulation with LPS on Expression of High Mobility Group Box1 in Murine Peritoneal Macrophages
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摘要 目的观察脂多糖(LPS)刺激对小鼠腹腔巨噬细胞高迁移率族蛋白B1(HMGB1)表达的影响。方法取正常Swiss小鼠腹腔巨噬细胞,以LPS分别刺激4、8、12、18、24和36h后,RT-PCR法检测小鼠腹腔巨噬细胞HMGB1基因mRNA的转录水平,Western blot法检测HMGB1蛋白的表达水平,观察LPS刺激与HMGB1释放的时效关系。结果LPS刺激后4~18h,细胞内HMGB1基因mRNA的转录水平无明显变化,24h开始明显增强,刺激24h和36h与对照组相比,差异有统计学意义,HMGB1蛋白在LPS刺激后18h开始表达明显增加,并一直持续至36h。结论LPS可促进小鼠腹腔巨噬细胞HMGB1的表达,并具有时间依赖性。 Objective To observe the effect of stimulation with LPS on the expression of high mobility group box 1 (HMGB1) in murine peritoneal macrophages. Methods The peritoneal macrophages of normal mice were isolated and stimulated with LPS for 4, 8, 12, 18, 24 and 36 h respectively, then determined for transcription level of HMGB1 mRNA by RT-PCR and for expression level of HMGBI protein by Western blot. The time-response relationship between LPS stimulation and HMGB1 release was observed. Restilts The transcription level of HMGB1 mRNA showed no significant change 4 - 18 h, while increased significantly 24 h and showed significant difference with those of control 24 and 36 h after LPS stimulation. However, the expression level of HMGB1 protein increased significantly from 18 h until 36 h after LPS stimulation. Conclusion LPS showed a time-dependent promoting effect on the expression of HMGB1 in murine peritoneal macrophages.
出处 《中国生物制品学杂志》 CAS CSCD 2009年第8期768-770,共3页 Chinese Journal of Biologicals
基金 吉林大学种子基金资助项目(701046)
关键词 脂多糖 巨噬细胞 高迁移率族蛋白B1 表达 Lipopolysaccharide ( LPS ) Macrophage High mobility group box 1 ( HMGB 1 ) Expression
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  • 1姜南艳,于文彬,苏明权,李斌,郝晓柯,李立文.HMGB1B盒编码序列的克隆和大肠杆菌表达[J].第四军医大学学报,2005,26(3):199-201. 被引量:2
  • 2姚咏明,刘辉.对高迁移率族蛋白B1作用的新认识[J].中国危重病急救医学,2005,17(7):385-387. 被引量:60
  • 3朱明光,常雅萍.高迁移率族蛋白B1的致炎细胞因子作用研究进展[J].国际免疫学杂志,2006,29(4):257-260. 被引量:15
  • 4Li J,Kokkola R,Tabibzadeh S,et al.Structural basis for the proinflammatory cytokine activity of high mobility group box 1.Mol Med,2003,9(1-2):37
  • 5Andersson U,Wang H,Palmblad K,et al.High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes.J Exp Med,2000,192 (4):565
  • 6Brown GC,Borutaite V.Nitric oxide,cytochrome c and mitochondria.Biochem Soc Symp,1999,66(1):17
  • 7Ayala A,Chaudry IH.Immune dysfunction in murine polymicrobial sepsis:mediators,macrophages,lymphocytes and apoptosis.Shock,1996,6(Suppl):S27
  • 8Kokkola R,Andersson A,Mullins G,et al.RAGE is the major receptor for the proinflammatory activity of HMGB1 in rodent macrophages.Scand J Immunol,2005,61(1):1
  • 9Helms J B, Zurzolo. Lipids as targeting signals: lipid rafts and intracellular trafficking. Traffic, 2004,5 (4): 247-254.
  • 10Kosugi A, Sakakura J, Yasuda K, et al. Involvement of SHP-1 tyrosine phosphatase in TCR-mediated signaling pathways in lipid rafts[J]. Immunity,2001,14:669-680.

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  • 1王效英,张旗,王强,陈卓,陈智.胞内信号转导分子LIM矿化蛋白1在人牙髓细胞体外矿化过程中表达的实验研究[J].口腔医学研究,2006,22(3):228-231. 被引量:11
  • 2Mitsiadis TA, Feki A, Papaccio G, et al. Dental pulp stem cells, niches, and notch signaling in tooth injury[J]. Adv Dent Res, 2011,23(3) : 275-279.
  • 3Kim JK, Shukla R, Casagrande L, et al. Differentiating dental pulp cells via RGD-dendrimer conjugates[J]. J Dent Res, 2010,89(12) : 1433-1438.
  • 4Tamai K, Yamazaki T, Chino T, et al. PDGFRalpha-posi- tive cells in bone marrow are mobilized by high mobility group box 1 (HMGB1) to regenerate injured epithelia[J]. Proc Natl Acad Sci USA, 2011,108(16) : 6609-6614.
  • 5Biscetti F, Ghirlanda G, Flex A. Therapeutic potential of high mobility group box- 1 in ischemic injury and tissue re- generation[J]. Curr VasePharmacol, 2011,9(6) : 677-681.
  • 6Wang L, Li S, Jungalwala FB. Receptor for advanced glyca- tion end products (RAGE) mediates neuronal differentiation and neurite outgrowth[J]. J Neurosci Res, 2008,86 (6) 1254-1266.
  • 7Livak KJ, Schmittgen TD. Analysis of relative gene expres- sion data using real-time quantitative PCR and the 2(-Del- ta Delta C(T)) Method[J]. Methods, 2001,25(4) : 402- 408.
  • 8Feghali K, Iwasaki K, Tanaka K, et al. Human gingival fi- hroblasts release high - mobility group box - 1 proteinthrough active and passive pathwaysrJ]. Oral Microbiol Im- munol, 2009,24(4) : 292-298.
  • 9Qin W, Lin ZM, Deng R, et al. p38a MAPK is involved in BMP-2- induced odontoblastic differentiation of human dental pulpcells[J]. IntEndodJ, 2012,45(3): 224-233.
  • 10Lee SY, Kim SY, Park SH, et al. Effects of recombinant dentin sialoprotein in dental pulp cells[J]. J Dent Res, 2012, 91(4) : 407-412.

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