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作 者:崔心刚[1] 安瑞华[2] 王立明[3] 朱有华[3] 梅长林
机构地区:[1]第二军医大学长征医院泌尿外科解放军泌尿外科中心,上海200003 [2]哈尔滨医科大学附属第一医院泌尿外科,哈尔滨150001 [3]第二军医大学长征医院器官移植科解放军器官移植研究所,上海200003 [4]长征医院肾内科,解放军肾脏病研究所
出 处:《第二军医大学学报》2006年第11期1174-1177,共4页Academic Journal of Second Military Medical University
基 金:黑龙江省博士后基金(LRB04-228);第二军医大学长征医院"三重三优"优秀青年后备人才基金~~
摘 要:目的:探讨基质金属蛋白酶1(MMP1)/组织金属蛋白酶抑制因子(TIMP1)在正常肾脏、常染色体显性遗传性多囊肾病(ADPKD)肾脏以及肾移植平均(2.5±1.2)年后切除的ADPKD肾组织中的表达差异。方法:用基因表达谱芯片筛选正常肾脏、ADPKD肾脏及肾脏移植后ADPKD肾脏的差异表达基因;以RT-PCR法验证其中差异表达的MMP1/TIMP1。结果:基因芯片筛选发现在正常肾组织与ADPKD肾组织中存在463条差异表达基因,肾移植后ADPKD肾组织对比ADPKD肾组织存在130条差异表达基因。筛选结果表明ADPKD以及肾移植后ADPKD肾脏MMP1/TIMP1表达较正常肾组织明显上调(P<0.05),而前两者间无显著差异。RT-PCR法证实MMP1/TIMP1在ADPKD肾脏以及肾移植后ADPKD肾组织中的表达均明显上调,明显高于正常肾脏组织(P<0.05),而前两者间无显著差异。结论:ADPKD的病理改变可能与MMPs/TIMPs基因表达失衡有关,MMPs抑制剂可能会对其有一定的治疗作用。Objective: To investigate the differential expression of matrix metalloproteinases-1 / tissue inhibitor of metalloproteinase-1 (MMP-1/TIMP-1) between normal kidney,kidneys of patients with autosomal dominant polycystic kidney disease (ADPKD), and the original kidneys after renal transplantation(OKRT). Methods: DNA microarray technique was used to analyze the differential gene expression in the above 3 tissues. Semi-quantitive RT-PCR was performed to verify the differentially expressed genes. Results: There were 463 differentially expressed genes between normal kidney and ADPKD tissues and 130 differentially expressed genes between ADPKD and the OKRT tissues. Expression of MMP1/TIMP1 in the ADPKD and the OKRT tissues were significantly higher than that in the normal kidney tissue (P〈0.05), with no significant difference found between the former 2 groups. Results of RT-PCR were consistent with the microarray findings. Conclusion: The pathogenesis of ADPKD may be related with the high expression of MMPs/TIMPs and the inhibitor of MMPs may have therapeutic effect on ADPKD.
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