Arachidonic Acid Up‐Regulates and Prostaglandin E2 Down‐Regulates the Expression of Pancreatic‐Type Phospholipase A2 and Prostaglandin‐Endoperoxide Synthase 2 in Uterine Stromal Cells
Open Access
- 1 November 1996
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 241 (3) , 872-878
- https://doi.org/10.1111/j.1432-1033.1996.00872.x
Abstract
It is well known that arachidonic acid, as a substrate of prostaglandin G/H synthase (PGHS), is converted into prostaglandins of the two‐series. In this work, we attempted to determine whether arachidonic acid and prostaglandin E2 might regulate the expression of PGHS and the pancreatic‐type phospholipase A2(PLA2 I), which may be involved in the liberation of arachidonic acid from membrane phospholipids. For this purpose, we used the uterine stromal cell line U111 which produces prostaglandin E2 and expresses both the constitutive and inducible PGHS enzymes (PGHS1 and PGHS2) and PLA2 I. The results show that PGHS1 which is expressed at a high level in U111 cells, was not modified by arachidonic acid. The expression of PGHS2 and PLA2 I was up‐regulated by increasing arachidonate concentrations (10–10 μM). The maximal response was obtained at 24 h, reaching a 2.3‐fold and 2.6‐fold increase for PGHS2 and PLA2 I expression, respectively, compared to the control level. To discriminate between the effect of arachidonic acid and that of prostaglandins, which are highly increased in the presence of exogenous arachidonic acid, we treated the cells with two inhibitors of PGHS activity, aspirin and meclofenamic acid. Both inhibitors failed to suppress the arachidonate‐induced increase of PLA2 I and PGHS2 expression and even enhanced it either in the presence or absence of arachidonic acid. In contrast, the addition of prostaglandin E2 to the culture medium decreased the expression of both enzymes in a dose‐dependent manner, the maximal response being reached at 1 μM. We conclude that arachidonic acid up‐regulates the expression of PLA2I and PGHS2 in the uterine stromal cells, independently of prostanoids, and that prostaglandin E2 is capable of down‐regulating enzyme expression.Keywords
This publication has 61 references indexed in Scilit:
- Biogenesis and Metabolic Fate of Docosahexaenoic and Arachidonic Acids in Rat Uterine Stromal Cells in CultureArchives of Biochemistry and Biophysics, 1996
- Detection and purification of two 14 kDa phospholipase A2 isoforms in rat kidney: their role in eicosanoid synthesisBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1995
- Regulated expression of prostaglandin endoperoxide synthase-2 by uterine stromaEndocrinology, 1994
- Studies on the induction of cyclooxygenase isozymes by various prostaglandins in mouse osteoblastic cell line with reference to signal transduction pathwaysBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1994
- Type II phospholipase A2 in human gestational tissues: extractable immuno- and enzymatic activity in fetal membranesBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1993
- Lipopolysaccharide-Induced Expression of Prostaglandin H Synthase-2 in Alveolar Macrophages Is Inhibited by Dexamethasone but Not by AspirinBiochemical and Biophysical Research Communications, 1993
- Immunohistochemical study of phospholipase A2 in boyine prostateThe Prostate, 1993
- Purification and characterization of phospholipase A2 from rat stomachBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1990
- Endometrial Prostaglandin E2 Binding During the Estrous Cycle and Its Hormonal Control in Ovariectomized Rats 1Biology of Reproduction, 1983
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970