## Abstract The stimulation of DNA synthesis in quiescent, density‐arrested BALB/c‐3T3 cells by platelet‐derived growth factor in plasma‐supplemented medium was inhibited by the presence of isobutylmethylxanthine (IBMX) and cholera toxin, although neither IBMX or cholera toxin when used alone inhib
Intracellular acidification inhibits the proliferative response in BALB/c-3T3 cells
✍ Scribed by C. A. Lucas; R. J. Gillies; J. E. Olson; K. A. Giuliano; R. Martinez; J. M. Sneider
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 734 KB
- Volume
- 136
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
One of the earliest events to occur upon the addition of serum to quiescent cells is an increase in the intracellular pH (pHin). The relationship between this pH change and proliferation is not known. In the present study, we investigate the consequences of acidifying the cytosol using the weak acid, 5', 5"-dimethyl oxazolidine 2,4-dione (DMO). At a concentration of 50 mM, DMO inhibits the serum-induced increases in pHin, DNA synthesis, and cell number. This concentration of DMO is shown not to inhibit the steady-state rate of mitochondrial respiration and not to inhibit DNA synthesis in a pH-independent fashion. The effects of DMO treatments are also shown to be reversible, indicating that this compound is not cytotoxic. These observations indicate that DMO inhibits cell proliferation by lowering intracellular pH. One important event that must occur prior to the initiation of DNA synthesis is an elevated rate of protein synthesis. The rate of protein synthesis in situ is extremely pH sensitive. Addition of 50 mM DMO to serum-stimulated cultures reduces the rate of leucine incorporation to unstimulated levels. These observations suggest that cytoplasmic acidification may inhibit proliferation through its effects on protein synthesis.
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