The growth regulation of human diploid fibroblasts by platelet-derived growth factor (PDGF), epidermal growth factor (EGF), insulin-like growth factor I (IGF-I) (somatomedin C), dexamethasone, and transferrin was investigated in a serumfree, chemically defined culture system. Cell-cycle kinetic para
Growth factor-induced proliferation of human fibroblasts in serum-free culture depends on cell density and extracellular calcium concentration
โ Scribed by Christer Betsholtz; Bengt Westermark
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 872 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0021-9541
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โฆ Synopsis
Abstract
Human neonatal skin fibroblasts plated sparsely in MCDB 105 traversed a complete cell cycle in the absense of serum or serumโderived proteins. Addition of pure PDGF did not significantly increase entrance into S phase as revealed by ^3^Hโthymidine labeling index or clonal growth on palladium islands. In subphysiologic Ca^2+^ concentrations or in the presence of a calmodulin inhibitor, W7, proliferation in the absence of growth factors ceased and PDGF became mitogenic. In contrast, confluent fibroblast cultures were stimulated by PDGF in physiologic Ca^2+^ concentrations. This was also the case with sparse adult skin fibroblast cultures while a fetal strain entered S in the absence of PDGF even in low extracellular Ca^2+^ concentrations. EGF gave similar results as PDGF in all experiments performed. This proposes a similar role for the two growth factors in the cell cycle. However, a difference in the mechanisms of action of PDGF and EGF is indicated by the fact that PDGF and EGF were additive at optimal concentrations when maximal growth response by a single growth factor was restricted by a subphysiologic extracellular Ca^2+^ concentration.
๐ SIMILAR VOLUMES
The influence of cell density and epidermal growth factor (EGF) on the expression and inducibility of cytochrome P450 (CYP) genes of the CYP3A and CYP1A families in adult human hepatocytes in primary culture has been evaluated. Only when cultured at subconfluence and in the presence of EGF did hepat