Eraiser T L, Khamzina L S
Laboratory of Immunochemistry, Cancer Research Center, Moscow, USSR.
Int J Cancer. 1988 Oct 15;42(4):633-7. doi: 10.1002/ijc.2910420427.
McA-RH 7777 hepatoma cells were cloned on 2 occasions a week apart (test cloning). Alpha-fetoprotein (AFP) phenotypes of primary and secondary clones from 55 primary clones were estimated. High interclonal heterogeneity of AFP expression was demonstrated. This variability exceeded by several orders of magnitude the mutation rate. We also found intraclonal differences in rates of variability. A "stabilizing" cloning was also carried out, aiming at the selection of AFP+ and AFP- stable cell lines. Stabilizing cloning included 7 cycles of cloning and selection of the most phenotypically stable clone. This stability was shown to be incomplete during the maintenance of clones in culture.
McA-RH 7777肝癌细胞每周克隆2次,间隔1周(试验性克隆)。对55个初级克隆的初级和次级克隆的甲胎蛋白(AFP)表型进行了评估。结果显示AFP表达存在高度的克隆间异质性。这种变异性比突变率高出几个数量级。我们还发现克隆内变异率存在差异。还进行了“稳定化”克隆,旨在筛选出AFP+和AFP-稳定细胞系。稳定化克隆包括7个克隆周期,并选择表型最稳定的克隆。结果表明,在培养过程中克隆的稳定性并不完全。