Abstract
A quiescent [denoted as Q(G0/G1)] subpopulation was isolated from EMT6/Ro-fed plateau monolayers by centrifugal elutriation. The median Coulter volume of these cells was significantly smaller than that of the original population from which they were elutriated. Using two-step acridine orange staining and dual parameter flow cytometric analysis, over 95% of quiescent cells were found to have G1 DNA content, and 80% of the cells had a decreased RNA content as compared to rapidly proliferating exponential G1 cells. After labeling for 24 hr (two doubling times) with [3H]thymidine, less than 2% of the quiescent cells incorporated [3H]thymidine as measured by autoradiography. The colony-forming efficiency of these cells was not significantly different from that of exponential cells. When such Q(G0/G1) cells were replated in fresh medium at a lower density, there was a lag time of 30 hr before any increase in cell number was detected, after which the cell-doubling rate matched that of exponential culture. Results obtained from the radiation dose-response curves showed that quiescent (G0/G1) cells were more radiosensitive than exponential G1 or unseparated fed plateau cells.
Footnotes
-
↵1 Presented in part at the 32nd Annual Meeting of the Radiation Research Society, March 1984, Orlando, FL. Supported by NIH Grants CA 11198, CA 11051, CA 20329, and CA 28329, and is based on work performed under Contract DEAC02-76EV03490 with the United States Department of Energy at the University of Rochester Department of Radiation Biology and Biophysics, and has been assigned Report DOE/EV/03490-2426. The Coulter Counter and channelizer used were donated by the Harry Gardner, Jr., Fund.
-
↵2 To whom requests for reprints should be addressed.
- Received August 20, 1984.
- Accepted December 4, 1984.
- ©1985 American Association for Cancer Research.