In an attempt to understand further the mechanism of the morphological and functional "reverse transformation" of CHO-K1 cells induced by dibutyryl adenosine cyclic 3',5'-monophosphate (cAMP) and testosterone, the kinetics of variation in the susceptibility of cells to rounding after the addition or deletion of dibutyryl cAMP and testosterone have been investigated. Changes in susceptibility to cell rounding upon removal of divalent cations or pulse exposure to concanavalin A were complete within 0.5–1 h after addition or deletion of drug. In comparison, the gross conversion of CHO-K1 cells from epithelial- to fibroblast-like morphology after drug treatment or the converse change after drug removal required 8 or 4 h, respectively. The effects on cell rounding are not caused by an effect of dibutyryl cAMP upon cell growth rate. Inhibitor experiments indicate that the changes investigated do not require continued RNA or protein synthesis and are not prevented by agents which depolymerize microtubules.
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1 November 1973
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November 01 1973
ANTAGONISM BY DIBUTYRYL ADENOSINE CYCLIC 3',5'-MONOPHOSPHATE AND TESTOSTERONE OF CELL ROUNDING REACTIONS
Brian Storrie
Brian Storrie
From the Eleanor Roosevelt Institute for Cancer Research, Department of Biophysics and Genetics, University of Colorado Medical Center, Denver, Colorado 80220
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Brian Storrie
From the Eleanor Roosevelt Institute for Cancer Research, Department of Biophysics and Genetics, University of Colorado Medical Center, Denver, Colorado 80220
Received:
May 17 1973
Revision Received:
July 25 1973
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1973 by The Rockefeller University Press
1973
J Cell Biol (1973) 59 (2): 471–479.
Article history
Received:
May 17 1973
Revision Received:
July 25 1973
Citation
Brian Storrie; ANTAGONISM BY DIBUTYRYL ADENOSINE CYCLIC 3',5'-MONOPHOSPHATE AND TESTOSTERONE OF CELL ROUNDING REACTIONS . J Cell Biol 1 November 1973; 59 (2): 471–479. doi: https://doi.org/10.1083/jcb.59.2.471
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