## Abstract We have investigated the effect of varying La^+3^ concentrations (0.01 mM to 2.0 mM) on membrane potential and electrolyte composition of Ehrlich ascites tumor cells. La^+3^ concentrations less than 0.02 mM had no effect. Above 0.02 mM, La^+3^ induced concentrationβdependent loss of ele
Electrolyte and non-electrolyte distribution in the ehrlich ascites tumor cells during the cell cycle
β Scribed by A. M. Dupre; H. G. Hempling
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 905 KB
- Volume
- 105
- Category
- Article
- ISSN
- 0021-9541
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β¦ Synopsis
Abstract
In a previous study, evidence was presented for changes in the state of water and osmotically active solutes during the cell cycle. Total water was constant at 82% (w/w), while the fraction of water that was osmotically active decreased from a maximum during S to a minimum at mitosis. Total Na^+^, K^+^, and C1^β^ in milliequivalents per liter of cell water remained constant. Therefore, electrolytes are sequestered in the osmotically inactive water. Evidence is now presented that Na^+^ exists primarily as one compartment, with a second, slower compartment appearing during S and disappearing during G2. Na^+^ is completely exchangeable during the entire cell cycle.
The distribution of other penetrating solutes was also investigated. When placed in hyperosmotic ethylene glycol solutions, cells first shrink, then swell to their original volumes. ^14^Cβethylene glycol distributes in 89% of cell water throughout the cell cycle. However, ^14^Cβurea distributes in anywhere from 86β100% of the cell water, depending on the stage in the cell cycle. Both solutes are at chemical equilibrium in water in which they are distributed, but they differ in their effects on cell volume. The final volume at which cells equilibrate in urea varies with the concentration of urea in the environment and with time into the cell cycle. Results suggest a loss of osmotically active particles or decreased osmotic activity of urea.
π SIMILAR VOLUMES
Using the double thymidine block technique, Ehrlich ascites tumor cells (ELD) carried i n continuous spinner culture have been synchronized. Simultaneous monitoring of :tH-thymidine incorporation, cell number and mitotic index yielded a cell cycle time of approximately 13.5 hours. This is composed o
The effect of extracellular Pi and arsenate on Pi-transport in Ehrlich ascites tumor cells has been studied. Pi-transport can be described by Michaelis-Menten kinetics; the maximal flux equal to 44 mmoles (kg cell water)-' hour-' and K m equal to 3.3 X 1 0 -4 M. Arsenate is a competitive inhibitor o
The increase in number of Ehrlich ascites tumor (EAT) cells was diminished significantly when the cell culture was treated with 1,000 IU/ml of recombinant mouse alpha or beta interferon (IFN). Microscopical observation revealed that almost all the cells showed bi-or multinuclear morphology 3 to 5 da
## Abstract Recent evidence implicates the volumeβregulated anion current (VRAC) and other anion currents in control or modulation of cell cycle progression; however, the precise involvement of anion channels in this process is unclear. Here, Cl^β^ currents in Ehrlich Lettre Ascites (ELA) cells wer