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TGF-β_1、BMP-7 mRNA在实验性肝纤维化中的表达及意义 被引量:4
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作者 黄宁 曾令兰 +1 位作者 李淑莉 苏凤菊 《微循环学杂志》 2007年第3期19-21,F0002,共4页
目的:检测转化生长因子β1(TGF-β1)、骨形态发生蛋白-7(BMP-7)mRNA在实验性大鼠肝纤维化中的表达,并研究其与病程的关系。方法:采用复合因素建立肝纤维化动物模型,HE染色观察肝脏组织病理表现,实时荧光定量逆转录-聚合酶链反应技术(Rea... 目的:检测转化生长因子β1(TGF-β1)、骨形态发生蛋白-7(BMP-7)mRNA在实验性大鼠肝纤维化中的表达,并研究其与病程的关系。方法:采用复合因素建立肝纤维化动物模型,HE染色观察肝脏组织病理表现,实时荧光定量逆转录-聚合酶链反应技术(RealTimeRT-PCR)检测TGF-β1、BMP-7mRNA的表达水平,并分析两指标与病程的相关性。结果:肝纤维化动物TGF-β1mRNA明显高于正常对照组,而BMP-7mRNA水平明显低于正常对照组。随着病程的延长,TGF-β1mRNA表达水平呈明显上升趋势,而BMP-7mRNA则呈下降趋势。结论:肝纤维化的进程与TGF-β1mRNA水平升高和BMP-7mRNA表达下降有一定关系。 展开更多
关键词 实验性肝纤维化 TGF-β1 BMP-7 MRNA 转化生长因子-Β protein Matrix 细胞外基质
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骨形成蛋白-7与肾脏关系的研究进展 被引量:1
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作者 赵燕俐 孙仲伦 《上海医学》 CAS CSCD 北大核心 2007年第10期789-791,共3页
1990年,Ozkaynak等和Celeste等先后从牛骨中筛选出一种新的蛋白,经氨基酸序列分析,证实两者为同一种蛋白,命名为骨形成蛋白(bone morphogenetic protein,BMP)-7。近年研究发现,BMP-7与肾脏关系密切,不仅是肾脏胚胎发育、形态... 1990年,Ozkaynak等和Celeste等先后从牛骨中筛选出一种新的蛋白,经氨基酸序列分析,证实两者为同一种蛋白,命名为骨形成蛋白(bone morphogenetic protein,BMP)-7。近年研究发现,BMP-7与肾脏关系密切,不仅是肾脏胚胎发育、形态维持所必需的,还对延缓多种肾脏疾病的进展极为重要。现就BMP-7在肾脏生理和病理中的作用综述如下。 展开更多
关键词 骨形成蛋白-7 肾脏疾病 氨基酸序列分析 protein BMP-7 胚胎发育 肾脏生理
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紫杉醇脂质体对宫颈癌HeLa细胞生长及其claudin-7表达的影响
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作者 曹利娜 陆晓媛 《徐州医学院学报》 CAS 2011年第4期242-244,共3页
目的 探讨注射用紫杉醇脂质体对人宫颈癌HeLa细胞增殖及claudin-7蛋白表达水平的影响.方法 体外培养人宫颈癌 HeLa细胞,采用 MTT法观察不同浓度紫杉醇脂质体(0.01、0.1、1、10、100 μmol/L)对HeLa细胞增殖的抑制作用;采用Western blo... 目的 探讨注射用紫杉醇脂质体对人宫颈癌HeLa细胞增殖及claudin-7蛋白表达水平的影响.方法 体外培养人宫颈癌 HeLa细胞,采用 MTT法观察不同浓度紫杉醇脂质体(0.01、0.1、1、10、100 μmol/L)对HeLa细胞增殖的抑制作用;采用Western blot法检测HeLa细胞claudin-7蛋白表达水平在不同浓度紫杉醇脂质体作用下的变化.结果 5个浓度的紫杉醇脂质体均能显著抑制HeLa细胞的增殖,且呈时间和剂量依赖性;Western blot显示HeLa细胞经不同浓度紫杉醇脂质体处理48 h后,随着紫杉醇脂质体浓度的增高,claudin-7蛋白表达逐渐减弱.结论 紫杉醇脂质体对宫颈癌HeLa细胞体外生长具有明显的抑制作用,HeLa细胞claudin-7蛋白的表达在紫杉醇脂质体影响下是下调的. 展开更多
关键词 人宫颈癌HELA细胞 紫杉醇脂质体 claudin-7蛋白
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Construction of Eukaryotic Expression Vector Containing B7-1/GFP Gene and Its Expression in Osteosarcoma Cell Line
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作者 宁旭 刘勇 +1 位作者 杨述华 傅德皓 《The Chinese-German Journal of Clinical Oncology》 CAS 2006年第2期141-143,共3页
Objective: To construct eukaryotic expression vector containing B7-1/GFP geneand study its expression in osteosarcoma cell line LM8. Methods: By using gene cloning technique, eukaxyotic expression vector pEGFP-C1 wa... Objective: To construct eukaryotic expression vector containing B7-1/GFP geneand study its expression in osteosarcoma cell line LM8. Methods: By using gene cloning technique, eukaxyotic expression vector pEGFP-C1 was used to construct the murine B7-1 recombinant plasmid (pEGFP-C1/B7). Recombinant plasmid was transfected into LM8 cells with liposome and was confirmed by restriction endonuclease digestion and DNA sequencing. The expression of the fusion protein was detected using fluorescence microscope and Western blot analysis. Results: The recombinant eukaryotic expression plasmid pEGFP-C1/B7 was successfully constructed, which was confirmed by DNA sequencing, RT-PGR and restriction enzymes analysis. The green fluorescent protein could be detected in the transfected LM8 with fluorescence microscope. The expected B7-1 and green fluorescent protein (GFP) fusion protein was detected by RT-PCR and Western blot. Conclusion: The eukaryotic expression vector containing B7-1/GFP gene was constructed successfully, and it could be expressed in LM8 after transfection. 展开更多
关键词 B7-1 gene green fluorescent protein gene recombination OSTEOSARCOMA
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Construction of a recombinant lentivirus containing human microRNA-7-3 and its inhibitory effects on glioma proliferation 被引量:3
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作者 Lun Dong Chongxu Han +4 位作者 Hengzhu Zhang Xuewen Gu Jian Li Yongkang Wu Xiaodong Wang 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第27期2144-2150,共7页
In the present study, we constructed a lentivirus, FIV-CMV-GFP-miR-7-3, containing the microRNA-7-3 gene and the green fluorescent protein gene, and used it to transfect human glioma U251 cells. Fluorescence microscop... In the present study, we constructed a lentivirus, FIV-CMV-GFP-miR-7-3, containing the microRNA-7-3 gene and the green fluorescent protein gene, and used it to transfect human glioma U251 cells. Fluorescence microscopy showed that 80% of U251 cells expressed green fluorescence. Real-time reverse transcription PCR showed that microRNA-7-3 RNA expression in U251 cells was significantly increased. Proliferation was slowed in transfected U251 cells, and most cells were in the G1 phase of the cell cycle. In addition, the expression of the serine/threonine protein kinase 2 was decreased. Results suggested that transfection with a lentivirus carrying microRNA-7-3 can effectively suppress epidermal growth factor receptor pathway activity in U251 cells, arrest cell cycle transition from GI phase to S phase and inhibit glioma cell growth. 展开更多
关键词 microRNA-7-3 LENTIVIRUS serine/threonine protein kinase 2 GLIOMA PROLIFERATION epidermal growthfactor receptor cell cycle neural regeneration
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弓形虫不同分离株致密颗粒蛋白基因的序列分析及其在大肠埃希菌中的表达 被引量:3
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作者 郑斌 郑焕钦 +4 位作者 何蔼 李卓雅 曹爱莲 张瑞琳 詹希美 《中国寄生虫学与寄生虫病杂志》 CAS CSCD 北大核心 2005年第2期100-105,共6页
目的分析弓形虫不同分离株致密颗粒蛋白7(densegranuleprotein,GRA7)基因的异同及在大肠埃希菌中表达致密颗粒蛋白。方法从弓形虫不同分离株(RH株、ZS2株和GT株)的基因组中特异地扩增出GRA7基因,将目的基因定向克隆至原核表达载体pGEX-4... 目的分析弓形虫不同分离株致密颗粒蛋白7(densegranuleprotein,GRA7)基因的异同及在大肠埃希菌中表达致密颗粒蛋白。方法从弓形虫不同分离株(RH株、ZS2株和GT株)的基因组中特异地扩增出GRA7基因,将目的基因定向克隆至原核表达载体pGEX-4T-1,转化大肠埃希菌JM109并测序。利用互联网上的在线工具CLUSTALW进行序列分析。异丙基-B-D-硫代半乳糖苷(IPTG)体外诱导pGEX-4T-1/GRA7重组质粒菌的表达,对表达的目的蛋白进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE),分别以抗抗谷胱甘肽巯基转移酶(GST)抗体、人抗弓形虫阳性血清为一抗进行Westernblotting分析。以纯化的重组蛋白作为包被抗原,ELISA法检测抗弓形虫阴性、阳性血清。结果弓形虫不同分离株GRA7的基因序列相同;pGEX-4T-1/GRA7重组质粒在大肠埃希菌中表达了目的蛋白,Westernblotting分析表明该蛋白为GST融合蛋白,且能被人抗弓形虫阳性血清所识别;ELISA结果表明该蛋白能与人抗弓形虫阳性血清、兔抗弓形虫阳性血清特异结合,而与抗弓形虫阴性血清无反应。结论弓形虫不同分离株GRA7基因具有高度保守性;GRA7基因在大肠埃希菌中以GST融合蛋白的形式得到表达,且该重组蛋白具有一定免疫反应性。 展开更多
关键词 大肠埃希菌 弓形虫 分离株 十二烷基硫酸钠-聚丙烯酰胺凝胶电泳 蛋白基因 blotting Western GST融合蛋白 分析及 GRA7基因 谷胱甘肽巯基转移酶 ELISA法检测 致密颗粒蛋白 protein 阳性血清 原核表达载体 重组质粒 重组蛋白
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Chaihushugan decoction exerts antiepileptic effects by increasing hippocampal glutamate metabolism in pentylenetetrazole-kindled rats 被引量:9
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作者 Yu Yunhong Xie Wei Wang Changjun 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2015年第6期659-665,共7页
OBJECTIVE: To investigate the antiepileptic effects of Chaihushugan decoction(CHSGD) in rats with pentylenetetrazole(PTZ)-induced seizures and to discuss the impact of CHSGD on glutamate metabolism, a hypothesized und... OBJECTIVE: To investigate the antiepileptic effects of Chaihushugan decoction(CHSGD) in rats with pentylenetetrazole(PTZ)-induced seizures and to discuss the impact of CHSGD on glutamate metabolism, a hypothesized underlying mechanism of seizure reduction.METHODS: Fifty Wistar rats were divided randomly into either control(n = 10) or experimental(n = 40)groups. Rats in the control group were administered physiological saline intraperitoneally. A subconvulsive dose of PTZ(35 mg/kg) was administered intraperitoneally to rats in the experimental group to induce seizures. The fully PTZ-kindled rats were then randomly divided into five subgroups(n = 8 each) based on the following treatment categories: physiological saline, VPA(200 mg/kg), CHSGD(2.5 g/kg), CHSGD(5 g/kg), or CHSGD(10 g/kg),administered orally once per day, respectively. On day 28 following initiation of drug treatment, seizures were monitored. The rats were then sacrificed, and hippocampal dissections were performed for subsequent studies.RESULTS: CHSGD significantly prolonged the latency of myoclonic, clonic, and tonic seizures, while decreasing overall seizure rates in the kindled rats.The measured concentrations of 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) amino]-2-deoxy-d-glucose(2-NBDG) and glutamate were significantly lower in the hippocampi of kindled rats in groups treated with CHSGD compared with those treated with PTZ alone. In addition, CHSGD was found to up-regulate both the expression of glutamate transporter-1(GLT-1) protein and the activity of glutamine synthetase(GS) in the hippocampi of kindled rats.CONCLUSION: These results suggest that CHSGD has antiepileptic effects on PTZ-induced seizures.The results further suggest an increase in glutamate metabolism at the synaptic cleft is a putative underlying mechanism of seizure reduction. 展开更多
关键词 Epilepsy PENTYLENETETRAZOLE Chaihushugan decoction 2-(N-(7-nitrobenz-2-oxa-1 3-diazol-4-yl)amino)-2-deoxyglucose Glutamic acid Glutamate plasma membrane transport proteins Glutamate-ammonia ligase
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