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Accepted Preprint first posted online on 29 September 2008

Journal of Endocrinology 2008;199:425.

Journal of Endocrinology (2008) In press
DOI: 10.1677/JOE-08-0237
© 2008 Society for Endocrinology
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RESEARCH

Regulation of Prostaglandin Biosynthesis by Interleukin-1 in Cultured Bovine Endometrial Cells

Michiyo Tanikawa, Hwa-Young Lee, Kikuko Watanabe, Magda Majewska, Dariusz Skarzynski, Dong-Seok Lee, Soo-Bong Park, Choon-Keun Park, Tomas Acosta and Kiyoshi Okuda

M Tanikawa, Graduate School of Natural Science and Technology, Laboratory of Reproductive Endocrinology, Okayama University, Okayama, Japan
H Lee, Graduate School of Natural Science and Technology, Laboratory of Reproductive Endocrinology, Okayama University, Okayama, Japan
K Watanabe, Division of Applied Life Science, Graduate School of Integrated Scince and Art, University of East Asia, Yamaguchi, Japan
M Majewska, Reproductive Immunology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland
D Skarzynski, Reproductive Immunology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Olsztyn, Poland
D Lee, Division of Animal Resources, Collegeof Animal Resource Science, Kangwon National University, Chuncheon, Korea, Republic of
S Park, Animal Science, National Institute of Animal Science, Seonghwan 330-801, Korea, Republic of
C Park, Department of Animal Biotechnology, College of Animal Life Science, Kangwon National University, Chuncheon, Korea, Republic of
T Acosta, Graduate School of Natural Science and Technology, Laboratory of Reproductive Endocrinology, Okayama University, Okayama, 700-8530, Japan
K Okuda, Graduate School of Natural Science and Technology, Laboratory of Reproductive Endocrinology, Okayama University, Okayama, Japan

Correspondence: Tomas Acosta, Email: acosta{at}cc.okayama-u.ac.jp

Abstract

Interleukin-1 (IL-1) is a potent stimulator of prostaglandin production in bovine endometrium. The aims of the present study were to determine the cell types responsible for the secretion of prostaglandin (PG)E2 and PGF2{alpha} in response to IL-1, and the intracellular mechanisms of IL-1 action. Cultured bovine endometrial cells were exposed to IL-1{alpha} or IL-1β for 24 h. IL-1{alpha} and IL-1β stimulated PGE2 and PGF2{alpha} production in the stromal cells, but not in the epithelial cells. The stimulatory effect of IL-1{alpha} on PG production was greater than that of IL-1β. Stimulatory action of IL-1{alpha} on PG production was augmented by supplementing arachidonic acid (AA). When the stromal cells were incubated with IL-1{alpha} and inhibitors of phospolipase (PL) C or PLA2 (anthranilic acid; 1 µM), only PLA2 inhibitor completely stopped the stimulatory action of IL-1{alpha} on prostaglandin production. Moreover, a specific cyclooxygenase-2 (COX-2) inhibitor blocked the stimulatory effect of IL-1{alpha} on PG production. IL-1{alpha} (0.06 nM) promoted COX-2 and microsomal PGE synthase-1 (PGES1) gene and its protein expression. The expression of COX-1, PGES2, PGES3 and prostaglandin F synthase (PGFS) mRNA was not affected by IL-1{alpha} in the stromal cells. The overall results indicate that 1) the target of IL-1{alpha} and IL-1β for stimulating PG production is the stromal cell, 2) IL-1{alpha} is far more potent stimulator than IL-1β, 3) the stimulatory effect of IL-1{alpha} on PG production is mediated via the activation of PLA2 and COX-2, 4) IL-1{alpha} induced PG production by increasing expressions of COX-2 and PGES1 mRNAs and their proteins in bovine stromal cells.







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