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J. Biol. Chem., Vol. 263, Issue 16, 7567-7573, Jun, 1988
GK Bandyopadhyay, W Imagawa, DR Wallace and S Nandi
Linoleate metabolism via the cyclooxygenase pathway enhances the
proliferation of mammary epithelial cells in serum-free culture in the
presence of epidermal growth factor and insulin (Bandyopadhyay, G.K.,
Imagawa, W., Wallace, D., and Nandi, S. (1987) J. Biol. Chem. 262, 2750-
2756). Prostaglandin E2 (PGE2) can fully substitute for linoleic acid
provided endogenous hydroxyeicosatetraenoic acids (HETEs, lipoxygenase
metabolites) are available. The PGE2 effect is partial if lipoxygenase
activity is inhibited by nordihydroguaiaretic acid. Any combination of two
HETEs out of three tested (5-, 12-, and 15-HETEs) stimulates growth
synergistically with PGE2; and together (i.e. PGE2 + HETEs), they
completely substitute for linoleate. In the absence of PGE2, maximal
stimulation cannot be attained with HETEs. Exogenous 5-HETE, compared with
12- or 15-HETE, is preferentially incorporated by the mammary epithelial
cells, and about 25-30% of it is retained esterified in phospholipids. The
cellular level of nonesterified, free HETE is low. Radioimmunoassay
revealed that the concentrations of 12- and 15-HETEs in the culture media
(with or without added linoleate) were always higher than that of 5-HETE.
Both intra- and extracellular free HETEs are rapidly metabolized by the
cells. Since these cells are capable of producing eicosanoids from
linoleate, periodic supplementation of the cultures with linoleate allows
maintenance of higher HETE and PGE2 levels. Thus, it appears that not only
are HETEs short-lived in the cell cultures, but cells handle 5-HETE
differently than 12- and 15- HETEs. Whatever may be the pathways of
interaction, synergism between HETEs and PGE2 seems to explain how
linoleate stimulates the growth of mammary epithelial cells in the presence
of epidermal growth factor and insulin.
Proliferative effects of insulin and epidermal growth factor on mouse mammary epithelial cells in primary culture. Enhancement by hydroxyeicosatetraenoic acids and synergism with prostaglandin E2
Cancer Research Laboratory, University of California, Berkeley 94720.
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