期刊文献+

重症肌无力中枢损害模型大脑基因表达差异 被引量:1

Gene Expression of Pallium in Experimental Autoimmune Myasthenia Gravis with Dysfunction of Central Nervous System
在线阅读 下载PDF
导出
摘要 目的 探讨 SD大鼠重症肌无力 ( myasthenia gravis,MG)中枢神经系统 ( CNS)损害模型大脑皮质基因表达的差异 ,为深入研究 MG的 CNS损害机制提供实验依据。方法 将从 MG患者和非 MG患者血清中提取的免疫球蛋白分别注入实验组和对照组 SD大鼠侧脑室 ,3周后取新鲜脑组织提取 m RNA并分析基因表达的差异 ,将所得的差异表达基因在 Gene Bank中分析。结果 在 2 0 0 0条目的基因中共发现差异表达基因 46条 ,包括全长表达基因 1 7条 ,表达序列标识 2 9条。其中 42条表达减少 ,4条表达增加。差异表达基因包括信号转导相关基因、氨基酸及微量元素代谢相关基因、蛋白转运相关基因、细胞周期相关基因、细胞骨架和运动蛋白基因、免疫相关基因、蛋白质修饰相关基因、DNA结合蛋白及转录起始因子基因、离子通道相关基因等。结论 多种基因与 MG CNS损害相关 ,差异基因表达的检测结果可为深入研究 MG的发病机制提供新思路。 Objective To seek experimental evidence for the pathogenesis of the dysfunction of central nervous system (CNS) in myasthenia gravis (MG) by analyzing the gene expression of the pallium in experimental autoimmune myasthenia gravis models with dysfunction of CNS in SD rats. Methods The immunoglobulin derived from the sera of the MG patients and those of the healthy were injected into the lateral ventricles of the experimental SD rats and the control group respectively. The mRNA from the fresh pallium of all rats was taken for cDNA microarray three weeks later. The genes with obviously variant expression were analysed in GeneBank database. Results Among 2000 genes there were 46 differences including 17 complete gene sequences and 29 ESTs, of which 42 expressed higher and 4 lower in the experimental pallium than the controlled group. The genes with obviously variant expression include signal transduction related genes, metabolism of amino acid or microelement related genes, protein transportation related genes, cell division cycle related genes, cytoskeleton and motor protein genes, immune related genes, modification of protein related genes, DNA binding protein or initiation of transcription related genes and ion channel related genes. Conclusions Many genes are involved in the onset of CNS dysfunction in MG.
出处 《中国神经免疫学和神经病学杂志》 CAS 2004年第4期193-196,共4页 Chinese Journal of Neuroimmunology and Neurology
基金 国家自然科学基金资助项目 ( 3 0 2 70 485 )
关键词 重症肌无力 中枢神经系统 基因芯片 基因表达 myasthenia gravis central nervous system cDNA microarray gene expression
  • 相关文献

参考文献5

  • 1刘睿,李柱一,许汉鹏,王者晋.重症肌无力AChRAb与培养神经元nAChR免疫结合反应研究[J].中国神经免疫学和神经病学杂志,2002,9(2):91-94. 被引量:18
  • 2李柱一,刘少峰,王者晋.重症肌无力CNS损害和神经细胞关系[J].中国神经免疫学和神经病学杂志,2002,9(2):99-102. 被引量:5
  • 3Huang D,Shi FD,Giscombe R,et al.Disruption of the IL-1 beta gene diminishes acetylcholine receptor-induced immune responses in a murine model of myasthenia gravis[J].Eur J Immunol,2001,31(1):225-232.
  • 4Borish L,King MS,Mascali JJ,et al.Transthyretin is an inhibitor of monocyte and endothelial cell interleukin-1 production[J].Inflammation,1992,16(5):471-484.
  • 5Lang B,Vincent A.Autoantibodies to ion channels at the neuromuscular junction[J].Autoimmun Rev,2003,2(2):94-100.

二级参考文献11

共引文献19

同被引文献13

  • 1王晓芳,李海峰,周红梅,朱元祺.中国人(汉族)MG患者FcγRⅢB基因多态性分析[J].中国神经免疫学和神经病学杂志,2005,12(2):63-66. 被引量:2
  • 2沈钢,柴(王莹),岳岚,魏红权,林敏.胸腺瘤伴重症肌无力患者瘤组织中Bcl-2和Fas的表达水平[J].中华结核和呼吸杂志,2006,29(4):240-242. 被引量:7
  • 3杨宏伟,孙兆林,张明义,王淑辉,李海峰,丛志强,高晓玉,谢琰臣.家族性重症肌无力与HLA-DQB1等位基因多态性的相关性[J].中华医学遗传学杂志,2006,23(4):437-439. 被引量:7
  • 4彭丹涛,许贤豪,佘子瑜.新斯的明试验改良结果判定法研究[J].中国神经免疫学和神经病学杂志,2007,14(1):1-3. 被引量:26
  • 5Melms A, Luther C, Stoeckle C, et al. Thymus and myasthenia griavis: Antigen processing in the human thymus and the consequences for the generation of autoreactive T cells [ J ]. Acta Neurol Scard Suppl, 2006,183 : 12 - 13.
  • 6Magic Z, Radulovic S, Brankovic-Magic M. cDNA microarrays: Identification of gene signatures and their application in clinical practice[J]. J BUON, 2007,12(Suppl 1 ) :S39 - S44.
  • 7Pan Q, Zhang ZB, Zhang X, et al. Gene expression profile analysis of the spontaneous reversal of rat hepaticfibrosis by cDNA microarray [ J]. Dig Dis Sci, 2007,52(10) :2591 -2600.
  • 8Aula P, Rapola J, Andersson LC. Distribution of cytoplasmic vacuoles in blood T and B lymphocytes in two lysosomal disorders [ J ]. Virchows Arch B Cell Pathol, 1975,18 (4) :263 - 271.
  • 9lorian V, Schltiter T, Bohnensack R. A new member of the sorting nexin family interacts with the C-terminus of P-selectin [ J]. Bionchem Biophys Res Commun, 2001,281 (4) :1045 -1050.
  • 10Green SA, Setiadi H, McEver RP, et al. The cytoplasmic domain of P-selectin contains a sorting determinant that mediates rapid degradation in lysosomes[ J]. J Cell Biol, 1994,124 (4) :435 -448.

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部