Suspension cultures of Chinese hamster cells (line CHO) were grown to stationary phase (approximately 8–9 x 105 cells/ml) in F-10 medium. Cells remained viable (95%) for at least 80 hr in stationary phase, and essentially all of the cells were in G1 Upon resuspension or dilution with fresh medium, the cells were induced to resume traverse of the life cycle in in synchrony, and the patterns of DNA synthesis and division were similar to those observed in cultures prepared by mitotic selection. Immediately after dilution, the rates of synthesis of RNA and protein increased threefold. This system provides a simple technique for production of large quantities of highly synchronized cells and may ultimately provide information on the biochemical mechanisms regulating cell-cycle traverse.
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1 July 1970
Article|
July 01 1970
REGULATION OF INITIATION OF DNA SYNTHESIS IN CHINESE HAMSTER CELLS : I. Production of Stable, Reversible G1-Arrested Populations in Suspension Culture
R. A. Tobey,
R. A. Tobey
From the Biomedical Research Group, Los Alamos Scientific Laboratory, University of California, Los Alamos, New Mexico 87544
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K. D. Ley
K. D. Ley
From the Biomedical Research Group, Los Alamos Scientific Laboratory, University of California, Los Alamos, New Mexico 87544
Search for other works by this author on:
R. A. Tobey
From the Biomedical Research Group, Los Alamos Scientific Laboratory, University of California, Los Alamos, New Mexico 87544
K. D. Ley
From the Biomedical Research Group, Los Alamos Scientific Laboratory, University of California, Los Alamos, New Mexico 87544
Received:
December 23 1969
Revision Received:
January 28 1970
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1970 by The Rockefeller University Press
1970
J Cell Biol (1970) 46 (1): 151–157.
Article history
Received:
December 23 1969
Revision Received:
January 28 1970
Citation
R. A. Tobey, K. D. Ley; REGULATION OF INITIATION OF DNA SYNTHESIS IN CHINESE HAMSTER CELLS : I. Production of Stable, Reversible G1-Arrested Populations in Suspension Culture . J Cell Biol 1 July 1970; 46 (1): 151–157. doi: https://doi.org/10.1083/jcb.46.1.151
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