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cDNA微阵列分析穿刺手术所致BALB/c小鼠肝损伤基因表达谱变化

Gene Expression Profile Change of Hepatic Injury in BALB/c Mouse Caused by cDNA Microarray Puncture Operation
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摘要 目的分析肝穿刺术后BALB/c小鼠肝脏基因表达谱的变化。方法10只BALB/c随机分为两组;实验组和正常组,每组各5只;实验组小鼠开腹直视下肝左叶注生理盐水,8天后采集肝组织标本并提取RNA,cDNA微阵列分析25 000个基因在实验组和正常组小鼠肝组织中的表达水平差异。结果肝穿刺术后共有82条差异基因,其中52条基因表达上调,30条基因表达下调;功能聚类可分为代谢、转录调节、转运、信号转导、炎症反应、细胞增殖与凋亡、细胞周期与细胞骨架及细胞粘附等8类。结论肝穿刺术所致小鼠肝脏基因表达谱发生的改变,涉及多个基因表达调控途径。 Objective To analyze mRNA expression profile of the liver in BALB/c mouse after liver puncture.Methods Ten BLAB/c mice were randomly divided into two groups: experimental group(5 mice) and normal group(5 mice).Liver puncture was performed by intra-hepatic injection of saline under a surgery microscope method.After 8 days,the mouse liver samples were collected and used to extract total RNA.The expression levels of approximately 25 000 genes were analyzed in the BALB/c mouse liver injected with saline comparing with the liver from normal group by cDNA microarray.Results The microarray showed that the expression levels of 82 genes were remarkably altered,52 of the genes were up-regulated and 30 genes were down-regulated.The altered genes were associated with metabolism,regulation of transcription,transport,signal transduction,inflammatory response,cell proliferation and apoptosis,cell cycle and cytoskeleton,cell adhesion and other processes.Conclusions Many differentially expressed genes with different functions interact with each other to resist liver injury by puncture.
出处 《地方病通报》 2010年第1期1-4,共4页 Endemic Diseases Bulletin
基金 国家自然科学基金资助项目(30760228 30860253) 新疆维吾尔自治区包虫病基础医学重点实验室开放课题项目(XJDX0202-2008-03)
关键词 CDNA微阵列 肝脏穿刺 损伤 cDNA microarray Liver puncture Injury
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  • 1Delahaye NF, Coltel N, Puthier D, et al. Gene - expression Profiling Discriminates between Cerebral Malaria (CM) - susceptible Mice and CM - resistant Mice [ J ]. J Infect Dis, 2006, 193(2) :312 -321.
  • 2Donati D, Mok B, Chelae A, et al. Increased B Cell Survival and Preferential Activation of the Memory Compartment by a Malaria Polyclonal B Cell Activator [J]. J Immunol, 2006, 177(5) :3035 -3044.
  • 3王康,戴勇,李德萍,吕天羽,唐敏,朱正.大鼠肾移植急性排斥反应时移植物中基因表达的研究[J].中华器官移植杂志,2006,27(11):660-663. 被引量:1
  • 4李劲松,聂君,陈刚,龚勇泉,江科,杨光海,刘磊,王建军.大鼠肺缺血再灌注损伤不同时期基因表达谱的改变[J].中华实验外科杂志,2008,25(2):200-202. 被引量:3
  • 5Friedman SL. Molecular Regulation of Hepatic Fibrosis, An Integrated Cellular Response to Tissue Injury [ J ]. J Bio Chem, 2000, 275:2247 - 2250.

二级参考文献16

  • 1Patterson GA. Indications. Unilateral, bilateral, heart-lung, and lobar transplant procedures. Clin Chest Med, 1997,18:225-230.
  • 2Eppinger M J, Deeb GM, Boiling SF, et al. Mediators of ischemia-reperfusion injury of rat lung. Am J Pathol, 1997,150:1773-1784.
  • 3Chudin E, Kruglyak S, Baker SC, et al. A model of technical variation of microarray signals. J Computational Biol,2006,13:996-1003.
  • 4Tamayo P, Slonim D, Mesirov J, et al. Interpreting patterns of gene expression with self-organizing maps: methods and application to hematopoietic differentiation. Proc Natl Acad Sci USA, 1999,96: 2907-2912.
  • 5Zwacka RM, Zhang Y, Halldorson J, et al. CD4^+ T-lymphocytes mediate ischemia/reperfusion-induced inflammatory responses in mouse liver. J Clin Invest,1997,100:279-289.
  • 6Hosenpud JD, Bennett LE, Keck BM, et al. The registry of the international society for heart and lung transplantation: seventeenth official report. J Heart Lung Transplant ,2000,19:909-931.
  • 7Basile DP, Fredrich K, Alausa M, et al. Identification of persistently altered gene expression in the kidney after functional recovery from ischemic acute renal failure. Am J Physiol Renal Physiol, 200,5288:953-963.
  • 8Nagano H, Nadeau KC, Takada M, et al. Sequential cellular and molecular kinetics in acutely rejecting renal allografts in rats.Transplantation, 1997,63 :1101.
  • 9Saiura A, Mataki C, Murakami T. A comparison of gene expression in murine carine cardiac allografts and isografts by means DNA microarray analysis. Transplantation, 2001,72:320-329.
  • 10Taylor GA, Jeffers M, Largaespada DA. Identification of a novel GTPase, the inducibly expressed GTPase,that accumulates in response to interferon-γ. J Biol Chem, 1996,271 : 20399-20405.

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