## Abstract Initiation of proliferation in densityβinhibited chick embryo fibroblast cultures induced by insulin or trypsin was partially reversed by replacing the medium with supernatants from parallel nonβstimulated cultures. Growth stimulation by neuraminidase, pokeweed mitogen, bacterial lipo p
The pattern of density dependent growth inhibition in murine fibroblasts
β Scribed by Mary C. P. Canagaratna; P. A. Riley
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 842 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0021-9541
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β¦ Synopsis
Abstract
Observations on the pattern of nuclear incorporation of ^3^HβTdR in long term (8βday) and short term (3βday) 3T3 cultures with local cell densities between 0.2 Γ 10^4^ and 6.2 Γ 10^4^ cells/cm^2^ are reported. Contrary to a number of previous studies our observations indicate that density dependent inhibition is exhibited in relatively sparse cultures, commencing at 0.5 Γ 10^4^ cells/cm^2^. Various possible mechanisms which could have caused the observed pattern of densityβdependent regression in labelling index are discussed.
π SIMILAR VOLUMES
## Abstract Various concentrations of oxygen were used to determine the optimum culture medium P for survival and proliferation of attached human and mouse fibroblasts grown from different inoculum sizes. When Tβ15 flasks were seeded with βͺ 2 Γ 10^4^ cells (βͺ 1.3 Γ 10^3^ cells/cm^2^), the highest p
## Abstract The multiplication rate of sparse cultures of chick embryo cells is only slightly lower at pH 6.9 than at pH 7.4. There is, however, a marked reduction in the multiplication rate of the pH 6.9 cultures before they reach confluency. Cultures at pH 7.4 continue to multiply beyond confluen
The effect of cell crowding on DNA synthesis (incorporation of 3HTdR and 32P04) was studied by an improved method in monolayers of secondary cells and established cell lines, either normal or transformed by viruses or carcinogens. The method was based mainly on pulse labeling of cultures of cells a
Using RNA in situ hybridization analysis, we have characterized the expression domains of the four known members of the FGF receptor-tyrosine kinase gene family in the murine hair follicle at various stages of the hair growth cycle. During anagen, we detected FgFl RNA in the dermal papilla, FgFZ RNA