Evaluation of the activity and localization of 15-lipoxygenase-1 after introduction into human colorectal carcinoma Caco-2 cells

Citation
Lc. Hsi et al., Evaluation of the activity and localization of 15-lipoxygenase-1 after introduction into human colorectal carcinoma Caco-2 cells, PROS LEUK E, 64(4-5), 2001, pp. 217-225
Citations number
30
Categorie Soggetti
Cell & Developmental Biology
Journal title
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS
ISSN journal
09523278 → ACNP
Volume
64
Issue
4-5
Year of publication
2001
Pages
217 - 225
Database
ISI
SICI code
0952-3278(200104/05)64:4-5<217:EOTAAL>2.0.ZU;2-E
Abstract
In human colorectal carcinoma Caco-2 cells, sodium butyrate (NaBT) induces the expression of the reticulocyte, 15-lipoxygenase-1 (15-LO-1) and causes these cells to undergo differentiation and apoptosis.15-LO-1 is also expres sed in human colorectal epithelium with a significant higher expression obs erved in colorectal tumors. In this study, we have prepared stable Caco-2 c ells that expressed 15-LO-1 under control of an inducible promoter. These c ells provide a model system to study regulation of 15-LO-1 activity in colo rectal cells without the interfering presence of NaBT and are useful to stu dy the biological function of 15-LO-1. The expressed 15-LO-1 was highly act ive as measured in cell lysates, but we were unable to detect metabolism in intact cells. The addition of calcium to the media for the Caco-2 cells wa s required for 15-LO-1 to translocate from the cytosol to the membrane whic h is frequently a requirement for lipoxygenase activity. Despite the additi on of calcium and translocation, little lipoxygenase activity was detected with intact cells. However, after removal of phenol red, a common constitue nt of cell culture media, we were able to detect 15-LO-1 activity in the tr ansfected Caco-2 cultured cells. Thus the presence of calcium and the absen ce of antioxidants present in commonly used culture media are required for expressed 15-LO-1 to be catalytically active and to permit an examination o f its biological effects. (C) 2001 Harcourt Publishers Ltd.