## Abstract Platelet‐derived growth factor (PDGF) and platelet‐poor plasma, which lacks PDGF, both induce a rapid increase in the rate of total protein synthesis within quiescent, density‐arrested Balb/c‐3T3 cells. This stimulation of protein synthesis is associated with an increased aggregation of
Control of the Balb/c-3T3 cell cycle by nutrients and serum factors: Analysis using platelet-derived growth factor and platelet-poor plasma
✍ Scribed by C. D. Stiles; R. R. Isberg; W. J. Pledger; H. N. Antoniades; C. D. Scher
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 982 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
Much controversy regarding the relationship between nutrients and serum in regulation of cell growth can be reconciled by recognizing that serum contains multiple factors which regulate different events in the cell cycle. Serum was fractioned into a platelet‐derived growth factor (PDGF), which induces cells to become competent to synthesize DNA, and plasma which allows competent cells to traverse G~0~/G~1~ and enter the S phase. Nutrients are not required for the cellular response to PDGF; however amino acids are required for plasma to promote the entry of PDGF‐treated, competent cells into S phase. The nutrient independent, PDGF‐modulated, growth regulatory event (competence) is located 12 hours prior to the G~1~/S phase boundary in quiescent, density‐arrested Balb/c‐3T3 cells. The nutrient dependent, plasma‐modulated event is located six hours prior to the G~1~/S phase boundary and corresponds in time to a plasma dependent growth arrest point. Moreover, plasma controls the concentration of amino acids required for DNA synthesis. Infection of density‐arrested Balb/c‐3T3 cells with SV40 overrides both the nutrient independent and the nutrient dependent growth regulatory events.
📜 SIMILAR VOLUMES
Platelet-derived growth factor (PDGF) and other agents that activate protein kinase C (PKC) rapidly alter cytosolic pH (pHJ and intracellular free calcium (Ca' +I,) in BALBk-3T3 fibroblasts. To define whether changes in pH, or [Ca++], are linked to PDGF-stimulated mitogenesis, these parameters were