QUANTITATIVE STUDIES OF THE GROWTH OF MOUSE EMBRYO CELLS IN CULTURE AND THEIR DEVELOPMENT INTO ESTABLISHED LINES

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.

[1]  H. Eagle,et al.  Myo-Inositol as an essential growth factor for normal and malignant human cells in tissue culture. , 1956, The Journal of biological chemistry.

[2]  I. Macpherson,et al.  Polyoma transformation of hamster cell clones--an investigation of genetic factors affecting cell competence. , 1962, Virology.

[3]  G. Yerganian,et al.  Maintenance of Normal in situ Chromosomal Features in Long-Term Tissue Cultures , 1961, Science.

[4]  K. Sanford,et al.  The growth in vitro of single isolated tissue cells. , 1948, Journal of the National Cancer Institute.

[5]  K. Hirschhorn,et al.  Culture of Human White Cells using Differential Leucocyte Separation , 1961, Nature.

[6]  T. Hsu MAMMALIAN CHROMOSOMES IN VITRO I. The Karyotype of Man , 1952 .

[7]  R. Dulbecco,et al.  VIRUS-CELL INTERACTION WITH A TUMOR-PRODUCING VIRUS. , 1960, Proceedings of the National Academy of Sciences of the United States of America.

[8]  T. Puck,et al.  GENETICS OF SOMATIC MAMMALIAN CELLS III. LONG-TERM CULTIVATION OF EUPLOID CELLS FROM HUMAN AND ANIMAL SUBJECTS , 1958 .

[9]  R. C. Parker,et al.  EFFECTS OF X-IRRADIATED FEEDER LAYERS ON MITOTIC ACTIVITY AND DEVELOPMENT OF ANEUPLOIDY IN MOUSE-EMBRYO CELLS IN VITRO. , 1963, Proceedings. Canadian Cancer Conference.

[10]  J. E. Shannon,et al.  The influence of inoculum size on proliferation in tissue cultures. , 1951, Journal of the National Cancer Institute.

[11]  T. Puck,et al.  Clonal growth of mammalian cells in vitro; growth characteristics of colonies from single HeLa cells with and without a feeder layer. , 1956 .

[12]  R. C. Parker,et al.  The karyotypes of cell lines recently established from normal mouse tissues. , 1959, The Journal of experimental zoology.

[13]  Rothfels Kh,et al.  EFFECTS OF X-IRRADIATED FEEDER LAYERS ON MITOTIC ACTIVITY AND DEVELOPMENT OF ANEUPLOIDY IN MOUSE-EMBRYO CELLS IN VITRO. , 1963 .

[14]  L. Hayflick,et al.  The serial cultivation of human diploid cell strains. , 1961, Experimental cell research.

[15]  H. Green,et al.  Repression of Growth of Mammalian Cells under Agar , 1962, Nature.

[16]  T. Hsu Chromosomal evolution in cell populations. , 1961, International review of cytology.

[17]  A. Levan,et al.  ROLE OF CHROMOSOMES IN CANCEROGENESIS, AS STUDIED IN SERIAL TISSUE CULTURE OF MAMMALIAN CELLS , 1958, Annals of the New York Academy of Sciences.

[18]  K. Piez,et al.  THE POPULATION-DEPENDENT REQUIREMENT BY CULTURED MAMMALIAN CELLS FOR METABOLITES WHICH THEY CAN SYNTHESIZE , 1962, The Journal of experimental medicine.

[19]  M. Abercrombie The bases of the locomotory behaviour of fibroblasts. , 1961, Experimental cell research.

[20]  H. Swim,et al.  Serial Propagation of 3 Strains of Rabbit Fibroblasts; Their Susceptibility to Infection with Vaccinia Virus.∗ , 1956, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[21]  D. Billen,et al.  Continuously Propagating Cells Derived From Normal Mouse Bone Marrow , 1960 .

[22]  A. Levan,et al.  Mammalian chromosomes in vitro. XV. Patterns of transformation. , 1961, Journal of the National Cancer Institute.

[23]  F. Ruddle Chromosome variation in cell populations derived from pig kidney. , 1961, Cancer research.

[24]  D. Filler,et al.  Isolation and serial propagation of malignant and normal cells in semi-defined media. Origins of CCRF cell lines. , 1960, Cancer research.

[25]  E. Shelton,et al.  Production of Malignancy in Vitro. V. Results of Injections of Cultures into Mice , 1943 .