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find Keyword "基因重组" 4 results
  • eNOS基因转染预防静脉移植血管再狭窄

    摘 要: 目的 应用含牛内皮型一氧化氮合成酶(eNOS)基因重组腺病毒(Ad5CMVNOSⅢ)转染静脉移植血管、观察eNOS基因预防静脉移植血管再狭窄的作用。方法 将21只杂种犬分为3组,手术对照组、Ad5CMVLac—Z(含大肠杆菌β半乳糖苷酶基因重组腺病毒)对照组和Ad5CMVNOSⅢ干预组。在犬颈静脉、颈动脉旁路血管移植术中分别应用Ad5CMVNOSⅢ病毒液或Ad5CMVLac—Z病毒液常温浸泡法感染静脉移植血管30分钟,术后28天病理切片观测移植血管新内膜增生状况。结果 与正常犬颈外静脉相比,手术对照组、Ad5CMVLac—Z对照组和Ad5CMVNOSⅢ干预组颈外静脉移植血管内膜/中膜比较均有不同程度增加(P<0.05),但Ad5CMVNOSⅢ组内膜/中膜比显著低于另外2个对照组(P<0.05),新内膜增生明显减轻。结论 Ad5CMVNOSⅢ感染静脉旁路移植血管对预防再狭窄有一定作用。

    Release date:2016-08-30 06:31 Export PDF Favorites Scan
  • PREPARATION OF rhBMP-2/BCB RECONSTITUTED BONE XENOGRAFT AND ASSAY OFITS OSTEOINDUCTIVITY

    Objective To investigate a new grafting material of bone xenograft with b bone inductive and conductive capacity. Methods Based on successful clinical application of the reconstituted bone xenograft (RBX), a new xenograft was made by combining recombinant human bone morphogenetic protein-2 (rhBMP-2) with antigen-free bovine cancellous bone (BCB). Sixty male BALB/C mice aged 4 weeks were divided into study group of 30 and control group of 30 randomly. rhBMP-2 / BCB was implanted in the left thigh muscle pouch in the study group andBCB in the control group. The mice were sacrificed at 7 d, 14d and 21d after implantation. Inductivity of rhBMP-2/BCB was detected by histological observation and biochemical determination of the samples. Results Histological examinationshowed that rhBMP-2/BCB induced chondrogenesis on the 7th day, with woven boneformed on the 14th day, and lamellar bone and marrow on the 21st day, while BCBfailed to induce chondrogenesis or osteogenesis on the 7th, 14th and 21st days. The alkaline phosphatase activities and calcium content in study group were higher than those in control group with significant difference (P<0.01). Conclusion rhBMP-2/BCB is an ideal grafting material with b bone inductive and conductive capacity without evoking immune reaction.

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  • 重组聚合酶链反应扩增乙型肝炎病毒跨直接重复序列区DNA片段方法的建立

    目的建立使用重组聚合酶链反应(PCR)扩增乙型肝炎病毒(HBV)跨直接重复序列(DR)区DNA 片段的方法。 方法使用Primer5 引物设计软件,以黏性末端为基础设计引物,HBV“大三阳”乙型肝炎表面抗原(+)、乙型肝炎核心抗体(+)、乙型肝炎e 抗原HBeAg(+)] 血清提取DNA 为PCR 模板,第1 轮PCR 分段扩增,第2 轮PCR 以粘性末端为引物两端补齐,第3 轮PCR 扩增整段HBV 跨DR 区DNA 片段。 结果成功重组出HBV跨DR 区缺口的DNA 片段。 结论建立了HBV 跨DR 区DNA 片段的扩增方法,为该段DNA 片段功能的研究打下了基础。

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  • Research status and prospect of echinococcosis-specific vaccine antigens

    Objective To summarize the research status of echinococcosis- specific vaccine antigens, analyze their sources and application prospects, and to provide new ideas for the development of echinococcosis vaccine antigens and drug treatment. Method Research on echinococcosis-specific vaccine antigens at home and abroad was searched and reviewed. Results Natural hydatid antigens, such as cystic fluid crude antigen, protoscolex segment, germinal layer, etc. often appear due to the difficulty of material acquisition and cumbersome preparation, resulting in unstable evaluation indicators such as sensitivity and specificity. The gene or protein sequences of a new recombinant hydatid antigen was accessible, the reproducibility and specificity were better, and it was more suitable for batch production testing, which was the main direction of current research, such as rAgB8/1, rEm18, rEm2, etc. Conclusions Vaccine development is one of the main directions for the elimination of hydatidosis. In the interaction between echinococcus and human or animal hosts, the natural structural proteins or excretion/secretion proteins of echinococcus stimulate the host to produce anti-parasites immunity and immune clearance, and the search for these specific protein antigens is of great significance for vaccine development, and new drug treatment.

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