## Abstract Short‐chain fatty acids, such as propionic, __n__‐butyric, __n__‐valeric, isovaleric, __n__‐caproic, and __n__‐caprylic acids, induce alkaline phosphatase activity in cultured mammalian cells. Long‐chain fatty acids have no similar effects. With B‐6 cells (mouse × Chinese hamster cell h
Alkaline phosphatase activity and the regulation of growth in transformed mammalian cells
✍ Scribed by Ben-Ami Sela; Leo Sachs
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 615 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
The relationship between alkaline phosphatase activity and cell growth has been studied in hamster cells transformed by different carcinogens. About 90% of normal hamster embryo cells were constitutively positive for alkaline phosphatase activity (AP^+^). However, there were no AP^+^ cells in cell lines transformed after treatment with the chemical carcinogens dimethylnitrosamine or 4‐nitro‐quinoline‐N‐oxide and 0.02% and 4% AP^+^ cells in cell lines transformed by polyoma virus or Simian virus 40. The glucocorticoid hormone, prednisolone, induced alkaline phosphatase activity in 12% and 44% of the enzyme‐negative (AP^−^) cells in cell lines transformed by polyoma or Simian virus 40, but this hormone did not induce alkaline phosphatase activity in AP^−^ cells from cell lines transformed after treatment with the chemical carcinogens. Treatment of polyoma transformed AP^−^ cells with the mutagen N‐methyl‐N′‐nitro‐N‐nitro‐soguanidine produced AP^+^ cells, whereas no AP^+^ cells were found after mutagen treatment of AP^−^ cells from the chemically transformed cell lines. Studies on spontaneous segregation in the polyoma transformed cell line has shown that AP^+^ cells segregated AP^−^ cells both in vitro and in vivo, although no spontaneous segregation was observed from AP^−^ to AP^+^ cells.
AP^+^ cells, compared to AP^−^ cells, showed a decrease in DNA synthesis, cell multiplication, the ability to form colonies in soft agar and tumorogenicity in animals. AP^−^ cells induced for alkaline phosphatase activity by prednisolone, showed the same growth properties in vitro as uninduced AP^−^ cells. The decreased cell growth found in AP^+^ cells which were constitutive for alkaline phosphatase activity was therefore not found in the hormone induced AP^−^ cells. The results indicate that constitutive alkaline phosphatase activity appears to be related to the regulation of cell growth and that AP^−^ cells have a selective advantage over AP^+^ cells.
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