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作 者:任奇杰 程龙[1] 孙颖飞[1] 贾元元[1] 刘晓明[1] 李勇[1]
机构地区:[1]宁夏大学生命科学学院/西部生物资源保护与利用教育部重点实验室,银川750021
出 处:《黑龙江畜牧兽医》2015年第11期232-235,294,共5页Heilongjiang Animal Science And veterinary Medicine
基 金:国家自然科学基金项目(31260615;31172278;31472191)
摘 要:为了建立豚鼠肺泡Ⅱ型上皮细胞(AECⅡ)分离、纯化和ROCK抑制剂培养的方法,进一步以AECⅡ为模型研究其在抗结核分枝杆菌中的免疫调控作用奠定基础,试验利用混合酶溶液全肺灌注法消化、分离含有豚鼠AECⅡ的混合细胞,经过红细胞裂解液处理与免疫黏附法纯化获得AECⅡ。以3T3细胞为饲养层,并添加Rho激酶抑制剂的方法进行AECⅡ的传代培养。结果表明:混合酶溶液灌注消化法能充分消化肺脏上皮细胞,通过Ig G免疫黏附能有效去除巨噬细胞而纯化AECⅡ,并且在3T3细胞饲养层与ROCK抑制剂培养条件下促进了AECⅡ的体外增殖而抑制其分化。To establish the method of isolation, purification and culture with Rho- associated protein kinase (ROCK) inhibitor of the type Ⅱ alveolar epithelial cells ( AEC Ⅱ ) from the guinea pig, and further lay a basis for the research on the immune regulation of AEC Ⅱ against Mycobacterium tuberculosis using AEC Ⅱ as a cell model. The mixed cells containing the AEC Ⅱ were digested and isolated by poured the mixed enzyme solution into the intact pulmonary, and then the AEC Ⅱ were obtained through the treatment of erythrocyte lysis buffer and the purification by immune adhering. The AEC Ⅱ were subcuhured with 3T3 feeder cells as a feeder layer and adding with ROCK inhibitor. The result showed that the pulmonary alveolar epithelial cells could be fully digested by perfusion digestion with the mixed enzyme solution. The AEC Ⅱ could be purified through immune adhering with IgG to efficiently remove the maerophages. The in vitro proliferation of AEC Ⅱ were promoted but their differentiation was inhibited under the culture conditions with 333 cell feeder layers and ROCK inhibitor.
关 键 词:豚鼠 肺泡Ⅱ型上皮细胞(AEC Ⅱ) 分离 培养 纯化
分 类 号:S865.11[农业科学—野生动物驯养] S852.5[农业科学—畜牧兽医]
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