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作 者:王飞[1] 朱郇悯[1] 韦雪梅[1] 刘嘉熙[1] 汤娟娟[1] 王嘉雯[1] 黎银燕[1] 陈晓湘[1] 李孜[1]
机构地区:[1]广州医科大学病原生物学与免疫学教研室,广东广州510182
出 处:《广州医学院学报》2013年第5期1-4,共4页Academic Journal of Guangzhou Medical College
基 金:广州市科技计划项目(2012J4100009);广州市重点学科建设项目(B127007)
摘 要:目的:表达、纯化重组肿瘤坏死因子相关凋亡诱导配体(TRAIL)的活性片段,并观察其对非小细胞肺癌细胞株的杀伤活性。方法:利用已有的pGEx-4T-l/TRAIL重组质粒转化BL21/DE3菌;异丙基-β-D-硫代半乳糖苷(IPTG)诱导表达谷胱甘肽转移酶(GST)标签的TRAIL,用GST-BIND树脂亲和层析柱纯化;SDS-PAGE电泳分析纯化结果;蛋白质超滤除盐、浓缩TRAIL;Bradford法定量。形态学观察肺癌细胞;乳酸脱氢酶(LDH)释放法确定TRAIL对肺癌细胞的杀伤活性。结果:共获得8.6 mg纯化TRAIL,其对A549、SPC-Al、HLAMP、95D、PGCL3、95C、H460等7株细胞株的IC50值分别为(2.33±0.22)μg/mL、(50.0±17.0)、(872.0±241.0)、(427.0±12.0)、(328.0±28.0)、(270.0±33.0)、(178.0±8.0)ng/mL。结论:相同组织类型的不同肺癌细胞株对重组TRAIL的敏感度不同,从低到高依次为A549、HLAMP、95D、PGCL3、95C、H460和SPCA1。Objective :To yield and purify the recombinant tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) active fragment, and to study the cytotoxic effects on non-small cell lung cancer (NSCLC) cell lines. Methods: The pGEX4T-1/TRAIL plasmid was transformed into BL21/DE3 bacteria. The IPTG was applied to induce the expression of TRAIL with GST tags (GST-TRAIL). This was followed by purification using GST-BIND resin high-affinity chromatography And SDS-PAGE eleetrophoresis. The products were desalinated and concentrated, followed by quantification by using Bradford' s technique. The morphological characteristics of lung cancer cells were determined, and the cytotoxic activity of TRAIL on lung cancer cells was assayed by using lactate dehydrogenase (LDH) release technique. Results: about a total of 8.6mg purified TRAIL was derived. The IC50 was (2.33 ± 0.22 ) μg,/ml for A549, (50.0± 17.0 ) ng/ml for SPCA1, ( 872.0± 240.0 ) ng/ml for HLAMP, ( 427.0 ± 12.0 ) ng/ml for 95 D, ( 328.0 ± 28.0 ) ng/ml for PGCL3, ( 270.0 ± 33.0 ) ng/ml for 95 C and (178.0± 8.0)ng/ml for H460, respectively. Conclusion: The different lung cancer cell lines have different sensitivity to TRAIL, as evidenced by the order of sensitivity of A549, HLAMP, 95D, PGCL3, 95C, H460 and SPC-A1.
关 键 词:肿瘤坏死因子相关凋亡诱导配体 肺癌 药物敏感度
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