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Quantitative Studies of the Growth of Mouse Embryo Cells in Culture and Their Development into Established Lines

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1963 May 1
PMID 13985244
Citations 913
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Abstract

Disaggregated mouse embryo cells, grown in monolayers, underwent a progressive decline in growth rate upon successive transfer, the rapidity of the decline depending, among other things, on the inoculation density. Nevertheless, nearly all cultures developed into established lines within 3 months of culture. The first sign of the emergence of an established line was the ability of the cells to maintain a constant or rising potential growth rate. This occurred while the cultures were morphologically unchanged. The growth rate continued to increase until it equaled or exceeded that of the original culture. The early established cells showed an increasing metabolic autonomy, as indicated by decreasing dependence on cell-to-cell feeding. It is suggested that the process of establishment involves an alteration in cell permeability properties. Chromosome studies indicated that the cells responsible for the upturn in growth rate were diploid, but later the population shifted to the tetraploid range, often very rapidly. Still later, marker chromosomes appeared. Different lines acquired different properties, depending on the culture conditions employed; one line developed which is extremely sensitive to contact inhibition.

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References
1.
Earle W, SANFORD K, Evans V, WALTZ H, SHANNON Jr J . The influence of inoculum size on proliferation in tissue cultures. J Natl Cancer Inst. 1951; 12(1):133-53. View

2.
Hastings J, Freedman S, RENDON O, Cooper H, Hirschhorn K . Culture of human white cells using differential leucocyte separation. Nature. 1961; 192:1214-5. DOI: 10.1038/1921214a0. View

3.
ROTHFELS K, Parker R . The karyotypes of cell lines recently established from normal mouse tissues. J Exp Zool. 1959; 142:507-20. DOI: 10.1002/jez.1401420123. View

4.
Ruddle F . Chromosome variation in cell populations derived from pig kidney. Cancer Res. 1961; 21:885-94. View

5.
Macpherson I, Stoker M . Polyoma transformation of hamster cell clones--an investigation of genetic factors affecting cell competence. Virology. 1962; 16:147-51. DOI: 10.1016/0042-6822(62)90290-8. View