Regulation of NIH‐3T3 cell G1 phase transit by serum during exponential growth
- 1 September 1995
- journal article
- Published by Wiley in Cell Proliferation
- Vol. 28 (9), 511-524
- https://doi.org/10.1111/j.1365-2184.1995.tb00089.x
Abstract
The proliferation rate of mammalian cells is regulated normally in the G1 phase of the cell cycle. During this phase, it is convenient to assign positive and negative roles to the molecular programs that regulate the duration of G1 and the phase transition from G1 to S phase. Density-dependent inhibition of cellular proliferation results in an increase in the duration of G1. This form of regulation is due to both secreted factors and cell-cell contact. Serum is mitogenic to a variety of mammalian cell types. Because quiescent cells enter S phase as a result of serum addition to culture media, serum is usually regarded as a source of positive regulatory growth factors. We have measured the length of the G1, S and G2+M phases of NIH 3T3 cells during exponential growth as a function of cell density and serum concentration. The G1 length increases during exponential growth as a function of density while S and G2+M are relatively constant. Further, this increase in G1 phase time, or density mediated negative regulation, is inhibited by increasing serum concentration. This phenotype is saturable between 10% to 20% serum. Serum concentrations above 2.5% are able to increase the rate of cell cycling (decrease the G1 phase time) by inhibiting density dependent negative regulation of NIH 3T3.Keywords
This publication has 21 references indexed in Scilit:
- The retinoblastoma protein and cell cycle controlCell, 1995
- Cyclins and cancer II: Cyclin D and CDK inhibitors come of ageCell, 1994
- G1 phase progression: Cycling on cueCell, 1994
- DP and E2F proteins: components of a heterodimeric transcription factor implicated in cell cycle controlCurrent Opinion in Cell Biology, 1994
- p27Kip1, a cyclin-Cdk inhibitor, links transforming growth factor-beta and contact inhibition to cell cycle arrest.Genes & Development, 1994
- Cell kinetic analysis of mixed populations using three‐color fluorescence flow cytometryCytometry, 1991
- Isolation and characterization of a 60-70-kD plasma membrane glycoprotein involved in the contact-dependent inhibition of growth.The Journal of cell biology, 1990
- Mitogen response and cell cycle kinetics of Swiss 3T3 cells in defined medium: Differences from human fibroblasts and effects of cell densityExperimental Cell Research, 1990
- Different quiescence states of three culture cell lines detected by acridine orange staining of cellular RNACytometry, 1988
- Analysis of intracellular antigens by flow cytometryCytometry, 1986