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PDL_1Ig基因修饰的恒河猴肝细胞在混合淋巴细胞反应中的效应研究 被引量:1
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作者 李鹏 张玉毅 +4 位作者 李恒平 丁正华 王毅 赵云 邓仲鸣 《免疫学杂志》 CAS CSCD 北大核心 2015年第1期32-35,共4页
目的探讨恒河猴来源的PDL1Ig在体外混合淋巴细胞反应中的作用。方法在Gen Bank中检索到恒河猴目的基因PDL1和Ig G1Fc的序列,采用重叠延伸PCR法合成该目的基因,与p GEM-T连接转化感受态E.coli TOP10,经鉴定得到PDL1Ig基因,p Shuttle-CMV... 目的探讨恒河猴来源的PDL1Ig在体外混合淋巴细胞反应中的作用。方法在Gen Bank中检索到恒河猴目的基因PDL1和Ig G1Fc的序列,采用重叠延伸PCR法合成该目的基因,与p GEM-T连接转化感受态E.coli TOP10,经鉴定得到PDL1Ig基因,p Shuttle-CMV线性化后连接目的基因转化感受态E.coli TOP10,克隆p Shuttle-CMV/PDL1Ig重组穿梭质粒。将p Ad Easy-1和线性p Shuttle-CMV/PDL1Ig共电转至BJ5183细胞中同源重组,构建重组腺病毒载体p Ad Easy-1/PDL1Ig骨架,以脂质体2000将p Ad Easy-1/PDL1Ig转染至293细胞中包装成有活性的重组腺病毒。感染恒河猴肝细胞,RT-PCR和Western blotting检测目的基因的表达。混合淋巴细胞反应(MLR)测定其生物学活性。结果成功构建了PDL1Ig重组腺病毒载体,能感染恒河猴肝细胞,RT-PCR和Western blotting检测有目的基因表达,在混合淋巴细胞反应中其能抑制T细胞增殖。结论成功构建了p Ad Easy-1/PDL1Ig重组腺病毒载体,其可在恒河猴肝细胞中高效表达,该重组蛋白可在体外通过PD-1/PDL1通路抑制T淋巴细胞增殖。 展开更多
关键词 恒河猴pdl1ig 腺病毒载体 混合淋巴细胞反应
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Expression of insulin-like growth factor-1 mRNA and protein level of corpora striata in ischemic side at the early stage of middle cerebral artery ischemia/reperfusion in rhesus monkeys
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作者 Huanmin Gao Rui Zhang Yunliang Guo 《Neural Regeneration Research》 SCIE CAS CSCD 2006年第2期133-136,共4页
BACKGROUND: Insulin-like growth factor-I(IGF-1), as one of the important members of growth factor family, participants in the regulation of many physiological functions and behaviors, having very strong neuroprotec... BACKGROUND: Insulin-like growth factor-I(IGF-1), as one of the important members of growth factor family, participants in the regulation of many physiological functions and behaviors, having very strong neuroprotective effect. However, the expression of IGF-1 following cerebral ischemia/reperfusion is still disputed. OBJECTIVE: To observe the expression of IGF-1 and protein of corpora striata in ischemic side at the early stage of middle cerebral artery ischemia/reperfusion in rhesus monkey. DESIGN : A completely randomized grouping design, controlled animal experiment SETTING : Institute of Cerebrovascular Disease, Affiliated Hospital of Medical College of Qingdao University MATERIALS: ① Totally 17 rhesus monkeys , of either gender, aged 4 to 5 years, were enrolled . Seven rhesus monkeys observed with gene chip were randomly divided into 2 groups: sham operation group (n=3) and ischemia/reperfusion group 〈n=4〉. Ten rhesus monkeys observed with in situ hybridization and immunohistochemistry method were randomly divided into 2 groups: sham operation group 〈n=3 〉and ischemia/reperfusion group (n=7). Rhesus monkeys observed under microscope were divided into 2 groups: sham operation group (n=6) and ischamia/reperfusion group (n=-11).②Materials used in the experiment: cresyl violet (Sigma Company, America); immunohistochemical reagent kit ( Huamei Bio-engineering Company); In situ hybridization reagent kit (Boshide Bio-engineering Co.Ltd, Wuhan); 12 800 dots chip (Boxing Company, Shanghai). METHODS : This experiment was carried out at the Institute of Cerebrovascular Disease, Affiliated Hospital of Medical College of Qingdao University from January 2001 to December 2003.① The onset area of middle cerebral artery was blocked for 2 hours, middle cerebral artery ischemia/reperfusion models were created.② After ischemia/reperfusion for 24 hours, cerebral tissue sections of rhesus monkeys were prepared and stained with cresyl violet. Image analysis was performed with 5001W image analysis software. Morphological change of corpora striata of operative side was observed in the rhesus monkeys between two groups. Total RNA was extracted from cerebral tissue. ③ Detection of gene chip: Cy3-duTP and Cy5-duTP were used to respectively perform reverse transcription labeling. The sample was reversely transcribed into cDNA, then hybridized with cDNA of cerebral tissue. Genes with the separate absolute value of cy3 and cy5〉800, cY3/cy5 〉 2(high expression) or 〈 0.5 (low expression) were found out. Those were genes with differential expression. ④ The expressions of IGF-1 mRNA and protein level of corpora striata in ischemic side of rhe- sus monkeys were detected between sham operation group and ischemia/reperfusion group at 9 and 24 hours after ischemia/reperfusion with in situ hybridization method and immunohistochemical method. Brown granules were IGF-1 protein positive cells. ⑤ Analysis of variance was used in the difference comparison of measurement data among groups. MAIN OUTCOME MEASURES : ① Change of morphological structure of corpora striata at ischemic side in rhesus monkeys. ② Change of cerebral gene expression profiles at ischemia/reperfusion in rhesus monkeys between two groups.③ Expression of IGF-1 mRNA and protein level of corpora striata at ischemia/reperfu- sion in rhesus monkeys between two groups. RESULTS : ① Pathological change : Obvious pathological change of cerebral infarction appeared in the ischemia and reperfusion group, while there was no such pathological change in the sham operation group.② Change of gene expression profile : There were 4480 genes with difference expression in the ischemia/reperfusion group and sham-operation group, in which, 260 genes had high expression and their absolute value was over 800, and 63 genes had low expression, cy3/cy5 of IGF-1 was 0.379, being relative low ex- pression. ③ IGF-1 mRNA and protein positive cell counts in corpora striata at cerebral ischemic side[IGF-1 mRNA: 〈9.72±1.18),(9.11 ±0.76),(14.77±0.60) counts/field:lGF-1 protein: (15.11 ±1.83),(15.39±0.78), (34.62±0.97)counts/field, P 〈 0.05-0.01]. CONCLUSION: IGF-1 mRNA and protein are lowly expressed in middle cerebral artery of rhesus monkeys at ischemia/reperfusion. 展开更多
关键词 ig Expression of insulin-like growth factor-1 mRNA and protein level of corpora striata in ischemic side at the early stage of middle cerebral artery ischemia/reperfusion in rhesus monkeys MRNA
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