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机构地区:[1]天津医科大学眼科中心,300070
出 处:《中华眼科杂志》2006年第8期744-750,共7页Chinese Journal of Ophthalmology
摘 要:目的为阻止白内障术后囊膜混浊寻找物质基础。方法提取灭活的白喉杆菌DNA和12周胎脑皮质RNA,应用聚合酶链反应(PCR)技术分别扩增出编码白喉毒素氨基端389个氨基酸(DT389)的基因片段及编码18 kd人碱性成纤维细胞生长因子(hbFGF)的基因全序列,将两基因先后插入表达载体中,构建含有DT389-hbFGF融合基因的表达质粒,测序后,转化大肠杆菌,IPTG诱导表达,纯化鉴定表达产物,噻唑蓝(MTT)试验检测其对体外培养人品状体上皮细胞(HLECs)的毒性作用,流式细胞术鉴定不同剂量融合毒素所致HLZCs成活率及细胞死亡形式。结果扩增得到DT389基因片段及hbFGF全基因序列;构建了DT389-hbFGF融合基因的原核表达载体并成功表达;表达的融合蛋白对HLECs有明显的毒性作用并在一定范围内呈明显剂量依赖性,半数致死量为3.8×10-11mol/L,所致细胞死亡方式主要以凋亡为主。结论DT389-hbFGF免疫毒素克隆表达的成功为药物促晶状体上皮细胞的凋亡、抑制后发障的研究奠定了物质基础。Objective To construct pGEX-DT389-hbFGF plasmid, express and identify the cytotoxicity to human lens epithelial cells(HLECs). Methods Extracting DNA of dead diphtheria bacillus and RNA of 12- week fetal brain cortex. The fragments of truncated diphtheria toxin (containing 389 amino acids of N-terminus, DT389 ) and full length human bFGF gene (encoding 18kd protein) were amplified by PCR technique respectively. The two fragments were inserted into prokaryotic expression vector pGEX-4T-1. After testing sequence, the expressing plasmid was transformed into E. Coli BL21 strain and induced expression under IPTG. The expressed fusion protein was purified and identified. MTr experiment tested cytotoxicity of the fusion protein to HLECs in vitro. The way of HLECs death under different dosage was identified by flow cytometry. Results The gene fragments of DT389 and human bFGF were accurately amplified. The expression vector including DT389-hbFGF fused gene was constructed and expressed successfully. DT389-hbFGF fusion protein can induce HLECs apoptosis in a dosage dependence manner during certain range. The LD50 was about 3.8 × 10^-11 mol/L. Conclusion The successful cloning and expression of DT389-hbFGF immunotoxin lay a foundation for accelerating lens epithelial cells apoptosis and the targeting therapy toward posterior capsule opacification. (Chin J Ophthalmol, 2006,42:744-750)
关 键 词:免疫毒素类 白喉毒素 成纤维细胞生长因子2 晶体 上皮细胞
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