Relation between the regulation of DNA synthesis and the production of two secreted glycoproteins by 12‐O‐tetradecanoylphorbol‐13‐acetate in 3T3 cells and in phorbol ester nonresponsive 3T3 variants
- 1 November 1986
- journal article
- research article
- Published by Wiley in Journal of Cellular Physiology
- Vol. 129 (2) , 151-158
- https://doi.org/10.1002/jcp.1041290205
Abstract
12-O-tetradecanolyphorbol-13-acetate (TPA), a potent tumor promoter, acts similarly to growth factors by selectively increasing the rate of production of the secreted proteins, mitogen regulated proteins (MRP) and major excreted protein (MEP) by murine 3T3 cells. MRP, a 34 kilodalton (kDa) glycoprotein, is a member of the prolactin-growth hormone family of proteins. MEP, a 39 kDa glycoprotein, is a lysosomal thiol protease that is also secreted. The aim of our investigation was to determine the relation between increases in MRP and MEP production and the initiation of DNA synthesis in response to mitogens. The TNR-9 cell lines is a variant of 3T3 cells in which growth factors, but not TPA and teleocidin, stimulate DNA synthesis and cell division. Usibng [35S]methionine to metabolically label proteins and SDS polyacrylamide gel electrophoresis to resolve the proteins, we found that growing cultures of 3T3 and TNR-9 cells responded equally well to TPA and teleocidin with increased rates of production of MRP and MEP. by conrast, the responses of quiescent TNR-9 cells to these tumor promoters in the increased production of MRP and MEP was greatly diminished compared with quiescent 3T3 cells. The changes in production of MRP in response to tumor promopters in quiescent and growing cells paralleled similar changes in the level of MRP mRNA. In summary, the ability to TPA and teleocidin to increase the rate of production of MRP and MEP correlated with the ability of these tumor promoters to stimulate DNA synthesis in quiescent 3T3 and TNR-9 cells. Evidently the biochemical condition that distinguishes TNR-9 from 3T3 cells and that limits the ability of tumor promoters to stimulate the production of MEP and MRP, and perhaps also DNA synthesis in TNR-9 cells occurs only when the cells are quiescent.This publication has 31 references indexed in Scilit:
- Glucose uptake and ornithine decarboxylase activity in tetradecanoyl phorbol acetate non-proliferative variantsJournal of Cellular Physiology, 1983
- Teleocidin is not mitogenic for 12-O-tetradecanoylphorbol-13-acetate non-proliferative variants of 3T3 cellsCarcinogenesis: Integrative Cancer Research, 1983
- Synergistic stimulation of S6 ribosomal protein phosphorylation and DNA synthesis by epidermal growth factor and insulin in quiescent 3T3 cellsCell, 1982
- Rapid selective stimulation by growth factors of the incorporation by Balbc 3T3 cells of [35S]methionine into a glycoprotein and five superinducible proteinsBiochemical and Biophysical Research Communications, 1982
- Stimulation of the release of two glycoproteins from mouse 3T3 cells by growth factors and by agents that increase intralysosomal pHBiochemical and Biophysical Research Communications, 1981
- Variants of 3T3 cells lacking mitogenic response to the tumor promoter tetradecanoyl‐phorbol‐acetateJournal of Cellular Physiology, 1981
- In Vitro Studies on the Mode of Action of the Phorbol Esters, Potent Tumor Promoters, Part 2CRC Critical Reviews in Toxicology, 1981
- Tumour promoter induces proliferation of 3T6 cells in serum-free medium, as do polypeptide growth factorsExperimental Cell Research, 1980
- In vitro studies on the mode of action of the phorbol esters, potent tumor promoters: Part 1CRC Critical Reviews in Toxicology, 1980
- Quantitative Film Detection of 3H and 14C in Polyacrylamide Gels by FluorographyEuropean Journal of Biochemistry, 1975