马蹄内翻足胎大鼠胫骨后肌组织的蛋白质组学分析  被引量:6

Proteomic analysis of tibia-fibulae musculature in rat fetus with talipes equinovarus

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作  者:周海涛[1] 孙开来[1] 富伟能[1] 吉士俊[2] 赵彦艳[1] 金春莲[1] 

机构地区:[1]中国医科大学医学遗传教研室,辽宁沈阳110001 [2]中国医科大学第二临床学院小儿外科,辽宁沈阳110003

出  处:《中国药理学与毒理学杂志》2005年第4期289-295,共7页Chinese Journal of Pharmacology and Toxicology

基  金:国家重点研究发展计划(973计划)基金资助项目(001CB510301)~~

摘  要:目的寻找马蹄内翻足畸形相关蛋白。方法提取全反式维A酸诱导的单纯马蹄内翻足畸形胎大鼠及正常对照胎大鼠胫骨后肌群总蛋白,进行双向电泳,考马斯亮蓝染色;经PDQuest软件分析,选择重复出现的差异点,质谱分析鉴定蛋白。结果获得了分辨率及重复性均好的双向电泳图谱。畸形胎大鼠与正常对照比较,有蛋白质点缺失、额外增加及明显上调或下调。质谱鉴定发现畸形胎大鼠肌组织慢骨骼肌肌钙蛋白T(sTnT)缺失,X连锁凋亡蛋白抑制因子(XIAP)下调,羧酸酯酶AY034877额外表达。结论畸形胎大鼠胫骨后肌组织与正常胎大鼠比较存在蛋白质组差异,畸形胎大鼠sTnT,XIAP及羧酸酯酶AY034877表达改变,可能与马蹄内翻足畸形相关。AIM To identify the particular proteins in the pathogenesis of talipes equinovarns (clubfoot)-like deformities. METHODS Pregnant rats were given all trans-retinoic acid 135 mg. kg- 1 at d 10 of gestation by a single intragastric infusion. Tibia-fibulae musculatures were removed from rat fetus on gestation d 21. Proteins were extracted with lysis solution (5 mol·L^-1 urea, 2 mol·L^-1 thiourea, 20 g·L^-1 CHAPS, 20 g· L^-1 SB3 - 10, 40 mol·L^-1 Tris, 0.2% BioLyte 3 - 10), 20 mL·g^-1 tissue. For two-dimensional electrophoresis, immobilized pH gradient gel (IPG, pH 3 - 10 and pH 5 - 8) iso-electric focusing was set as the first dimension, while 12% SDS polyacrylamide gel electrophoresis as the second dimension. Loaded sample sizes were 0.5 mg (350μL) for each pH 3 - 10 IPG strip and 1.0 mg for pH 5 - 8 IPG strip. Following electrophoresis, gels were stained with Coomassie brilliant blue. The images were analyzed with a PDQuest 7.0 software package. Spots with significant differences were subjected to mass spectrometry analysis. The peptide mass fingerprints were identified with protein databases (Swiss-Prot and NCBInr) using different softwares including PeptIdent, Mascot and MS-Fit. RESULTS Compared with those of the normal controls, samples of model rat fetus showed gaining and losing some spots with increase or decrease in intensity for a number of protein spots. A total of eight protein spots showed significant differences, and peptide mass fingerprints were acquired for seven among them. Three protein spots were identified by more than two softwares to give similar results, i. e. , loss of slow skeletal muscle troponin T( sTnT), Xlinked inhibitor of apoptosis(XIAP) and extra expression of carboxylesterase AY034877. CONCLUSION Proteomic difference between model and normal rat fetus can be well presented with 2D electrophoresis. Expression change of sTnT, XIAP and carboxylesterase AY034877 may be related to the pathogenetic mechanisms of talipes equinovarus.

关 键 词:马蹄内翻足 蛋白质组 模型 动物 

分 类 号:R682[医药卫生—骨科学]

 

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