## Abstract Chick embryo cells which have been kept overnight at pH 6.8 in the absence of serum multiply very slowly. Only a small fraction of cells is in the S period at any given time, and the rate of uptake of 2โdeoxyโDโglucose is very low. Upon raising the pH to 7.4 and adding serum (โturnโonโ)
Regulation of mitotic activity and the cell cycle in primary chick muscle cells by neurotransferrin
โ Scribed by Heinz Popiela; Daniel Taylor; Stanley Ellis; Robert Beach; Barry Festoff
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 714 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0021-9541
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โฆ Synopsis
Abstract
We previously demonstrated that neurotransferrin (NTF), a transferrin extracted from adult chicken peripheral nerves, promotes growth of primary chick muscle cells in the absence of embryo extract. NTF was shown to stimulate DNA synthesis and cell proliferation. In the present study, we demonstrate that NTF is a mitogen using two independent methods; counts of orceinโstained mitotic figures and analysis of cell cycle kinetics with a fluorescenceโactivated cell sorter. In lowโdensity cultures mitotic activity increases with increasing doses of NTF followed by a plateau at concentrations greater than 6 ฮผg/ml. Residual, embryonic mitotic activity progressively declines with time after plating muscle cells in the absence of NTF. Absence of NTF for 2 days causes cells to lose irreversibly their myogenic potential. In the presence of NTF, mitotic activity increases for 2 days followed by a decline concurrent with myoblast fusion and formation of myotubes. Cell cycle analysis showed that NTF addition causes cell populations to shift from G~t~ to S and G~2~ + M within 18.5 hr. Muscle cells, plated at high densities in the absence of NTF, show mitotic activities similar to those plated at low densities in the presence of NTF. Addition of NTF to highโdensity cultures is ineffective in stimulating mitosis. These studies show that at typical cell plating densities, NTF is a required mitogen for primary chick muscle cell cultures.
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