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作 者:田志刚[1] 孙汭[1] 张捷[1] 张建华[1] 刘杰[1] 田彤[1] 明雨[1] 崔正言[1]
出 处:《免疫学杂志》1994年第1期52-55,共4页Immunological Journal
基 金:国家自然科学基金
摘 要:应用MH60·BSF2细胞检测IL-6生物学效价时,存在该细胞饲养困难和长期培养容易变异而失去IL-6增殖依赖性等问题。为此我们首先探讨了克隆化筛选MH60·BSF2的方法,从增殖依赖性较差的MH60·BSF2细胞群体中筛选到3株IL-6强依赖细胞株。并探讨了该细胞的冻存复苏方法。所冻存的细胞半年以上亦无IL-6增殖依赖性的改变。在此基础上采用MTT比色法取代[ ̄3H]TdR掺入法获得成功,从而使IL-6待测标本的生物活性检测更为方便经济。In order to improve the method of IL-6 bicassay using IL-6 dependent cell line (MH60·BSF2).we es-tablished a cloning procedure and selected three clones of MH60·BSF2 whose proliferations were strongly dependent on IL-6,by comparison with uncloned MH60·BSF2. Meanwhile we stored the cloned MH60·BSF2 by cryogenic tech-nique. The cloned MH60·BSF2 cell line showed the same proliferating curve after cryogenic storage of half a year. We also developed the MTT coloy metric for MH60·BSF2 proliferation which showed the similar proliferating curve to the[ ̄3H]TdR method, The level of IL-6 of the culture supernant from different cells or cell line were measured. The results showed the PBMC of healthy individuals and of acute granulocyte leukemia secreted different value of IL-6(18u/ml and 234.67u/ml respectively);the human fetal gliocyets secreted high value IL-6(93.68u/ml).and LPS pro-moted the secretion of the gliocytes by about three folds.
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