期刊文献+

快速老化小鼠耳蜗组织MeCP2的增龄性变化 被引量:1

Age-related expression of mythl-CpG-binding protein-2 gene in the senescence accelerated mouse
下载PDF
导出
摘要 目的探讨快速老化小鼠听觉功能、以及耳蜗组织中甲基化结合蛋白-2(methyl-CpG-bindingprotein2,MeCP2)的增龄性变化。方法本研究选3、5、7、9月龄的快速老化小鼠亚系1(Senescence acceler-ated mouse/prone1,SAMP 1)作为实验组,而同龄抗快速老化亚系1(Senescence accelerated mouse/resistance 1,SAMR 1)作为SAMP 1的正常对照组。应用听觉诱发反应仪检测其听觉脑干反应阈值;应用RT-PCR和Western印迹杂交对耳蜗组织中MeCP2mRNA和蛋白的表达水平进行半定量分析。结果第7、9月龄SAMP1脑干反应阈值较同龄SAMR1明显增高(P<0.05);MeCP2 mRNA和蛋白在不同月龄快速老化小鼠耳蜗组织中均有表达,第7、9月龄SAMP1小鼠耳蜗组织中的MeCP2 mRNA和蛋白较同龄SAMR1小鼠明显降低(P<0.05)。结论MeCP2 mRNA和蛋白的表达水平随着快速老化小鼠听觉功能增龄性减退而降低,说明MeCP2可能与维持耳蜗的功能状态有关。 [Objective] The purpose of this study was to analyze age-related hearing loss in the senescence accelerated mouse and the expression of MeCP2 gene at mRNA and protein in the cochlea of the senescence accelerated mouse throughout development. [Methods] We chose the 3, 5, 7, 9th month as analyzing time points. The auditory thresholds and the expression of MeCP2 gene at mRNA and protein in the cochlea were studied in the senescence accelerated mouse/prone 1 (SAMP 1) at 3, 5, 7, 9 months. Normal aging Control the senescence accelerated mouse/resistance 1 (SAMR 1) was used. The expression of MeCP2 gene at mRNA level was analyzed by RT-PCR. The expression of MeCP2 protein was analyzed by Western blot. [Results] Auditory function evaluation: Compared with the SAMR 1, the SAMP 1 at 7, 9 months developed a progressive hearing loss at 8 kHz,which showed an agerelated significant increase (P 〈0.05). The expression of MeCP2 mRNA and MeCP2 protein in the cochlea: there were MeCP2 mRNA and MeCP2 protein expressed in the cochlea of the senescence accelerated mouse throughout the development. Compared with the SAMR 1, the SAMP 1 at 7, 9 months developed a significant descend (P 〈 0.05). [Conclusion] The expression level of MeCP2 mRNA and MeCP2 protein decreases when the senescence ac- celerated mouse develop a progressive hearing loss. This indicates that MeCP2 protein probably has relationship with maintaining functional status of the cochlea.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2009年第5期687-690,共4页 China Journal of Modern Medicine
基金 教育部春晖计划科研项目(No:Z2005-2-45002) 广西卫生厅科研项目(No:200746和Z2007193)
关键词 快速老化小鼠 听觉脑干反应阈值 耳蜗 甲基化结合蛋白-2 senescence accelerated mouse threshold of auditory brainstem response cochlea methyl-CpG- binding protein 2
  • 相关文献

参考文献11

  • 1IGNATIA B, VAN DEN VEYVER, AOGHBI HY. Genetic basis of Rett syndrome[J]. Mental Retard Dev Dis, 2002, 8: 82-86. 被引量:1
  • 2SHAHBAZIAN MD, ANTALFFY B, ARMSTRONG DL, et al. Insight into Rett Syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation[J]. Hum Mol Genet, 2002, 11(2): 115-124. 被引量:1
  • 3BALMER D, GOLDSTINE J, RAO YM, et al. Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal huamn brain development and is correlated with alternative polyadenylation[J]. J Mol Med, 2003, 81: 61-68. 被引量:1
  • 4MULLANEY BC, JOHNSTON MV, BLUE ME. Developmental expression of methyl-CpG-binding protein 2 is dynamicallu regulated in the rodent brain[J]. Neuroscinee, 2004, 123: 939-949. 被引量:1
  • 5CASSEL S, REVEL MO, KELCHE C, et al. Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study[J]. Neurobiol Dis, 2004, 15: 206-211. 被引量:1
  • 6ZOGHBI HY. Postnatal neurodevelopmental disorders: meeting at the synapse?[J]. Science, 2003, 302: 826-830. 被引量:1
  • 7张玉稚,潘虹,王汉森,包新华,吴希如.发育中Wistar大鼠大脑皮层甲基化结合蛋白-2基因表达变化[J].北京大学学报(医学版),2004,36(4):379-382. 被引量:1
  • 8BAO J, LEID, DU Y, et al. Requirement of nicotinic acetylcholine receptor subunit beta2 in the maintenance of spiral ganglion neurons during aging [J]. J Neurosci, 2005, 25: 23041-23045. 被引量:1
  • 9KUJOTH GC, HIONAA, PUGH TD, et al. Mitochondfial DNA mutations, oxidative stress, and apoptosis in mammalian aging[J]. Science, 2005, 309(5733): 481--484. 被引量:1
  • 10TAKUMIDA M, ANNIKO M. Radical scavengers: a remedy for presbyaeusis. A pilot study[J]. Acta Otolaryngol, 2005, 125(12): 1290-1295. 被引量:1

二级参考文献17

  • 1Amir RE, Van Den Veyver IB, Wan M, et al. Rett syndrome is caused by mutations on X-linked MECP2, encoding methyl-CpGbinding protein 2 [J]. Nat Genet, 1999, 23: 185 - 188 被引量:1
  • 2Ignatia B, Van Den Veyver,Aoghbi HY. Genetic basis of Rett syndrome[J]. Mental Retard Dev Dis, 2002, 8:82 -86 被引量:1
  • 3Pan H, Wang YP, Bao XH, et al. MECP2 gene mutation analysis in Chinese patients with Rett syndrome[J]. Eur J Hum Genet, 2002,10: 484 - 486 被引量:1
  • 4Nan X, Campoy FJ, Bird A. MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin [J]. Cell, 1997,88:471 -481 被引量:1
  • 5Shahbazian MD, Antalffy B, Armstrong DL, et al. Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation [J]. Hum Mol Genetics,2002,11:115 - 124 被引量:1
  • 6Chen RZ, Akbarian S, Tudor M, et al. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice[J]. Nat Genetics, 2001,27:327 -331 被引量:1
  • 7Reiss AL, Faruque F, Naidu S, et al. Neuroanatomy of Rett syndrome: A volumetric imaging study [J]. Ann Neurol, 1993, 34:227 - 234 被引量:1
  • 8Akbarian S, Chen RZ, Gribnau J, et al. Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex [J]. Neurobiology of disease, 2001,8:784 -791 被引量:1
  • 9Shahbazian MD, Zoghbi HY. Rett syndrome and MeCP2: Linking epigenetics and neuronal function [J]. Am J Hum Genet, 2002, 71:1259 - 1272 被引量:1
  • 10Guy J, Henddrich B,Holmes M, et al. A mouse MeCP2-null mutation causes neurological symptoms that mimic Rett syndrome[J]. Nat Genetics, 2001,27 (march) :322 - 326 被引量:1

同被引文献14

  • 1郭运凯,谢鼎华,杨新明.小鼠内耳3种溶酶体酶的定位及酶缺乏时的听力损害[J].中南大学学报(医学版),2006,31(1):79-84. 被引量:2
  • 2BEVAN S, WINTER J. Nerve growth factor (NGF) differentiallyregulates the chemosensitivity of adult rat cultured sensory neu- rons[J]. J Neurosci, 1995, 15(7): 4918-4926. 被引量:1
  • 3GILLESPIE LN, CLARK GM, MARZELLA PL. Delayed neu- rotrophin treatment supports auditory neuron survival" in deaf guinea pigs[J]. Neuroreport, 2004, 15(7): 1121- 1125. 被引量:1
  • 4SOMEYA S, XU J, KONDO K, et al. Age-related hearing loss in C57BL/6J mice is mediated by Bak-dependent mitochondrial apoptosis [J]. Proc Natl Acad Sci USA, 2009, 106 (46): 19432-19437. 被引量:1
  • 5FRIEDMAN RA, VAN LAER L, HUENTELMAN M J, et al. GRM7 variants confer" susceptibility to age-related hearing im- pairment[J]. Hum Mol Genet, 2009, 18(4): 785-796. 被引量:1
  • 6GOPINATH B, FLOOD VM, ROCHTCHINA E, et al. Serum homocysteine and folate concentrations are associated with prevalent age-related hearing loss [J]. The Journal of Nutrition, 2009, 140(8):1469-1474. 被引量:1
  • 7SCHW&NDER M, XIONG W, TOKITA J, et al. A mouse mod- el for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells [J]. PNAS, 2009, 106(13): 5252-5257. 被引量:1
  • 8RAMIREZ JJ, CALDWELL JL, MAJURE M, et al. Adeno-as- sociated virus vector expressing nerve growth factor enhances cholinergic axonal spouting after cortical injury in rats [J]. J Neurosci, 2003, 23(7): 2797-2803. 被引量:1
  • 9TUSZYNSKI MH, THAL L, PAY M, et al. A phase i clinical trial of nerve growth factor gene therapy for Alzheimer disease [J]. Nat Med, 2005, 11(5):551-555. 被引量:1
  • 10NIEWIADOMSKA G, KOMOROWSKI S, BAKSALERS- KA-PAZERA M. Amelioration of eholinergic neurons dysfunction in aged rats depends on the continuous supply of NGF [J]. Neu- robiol Aging, 2002, 23(4):601-613. 被引量:1

引证文献1

二级引证文献5

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