Michio Otsuki
Department School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine Position Professor and Division head |
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Article types | Original article |
Language | English |
Peer review | Peer reviewed |
Title | Specific regulation of lipocalin-type prostaglandin D synthase in mouse heart by estrogen receptor beta |
Journal | Formal name:Molecular endocrinology Abbreviation:Mol Endocrinol ISSN code:08888809 (Print)08888809 (Linking) |
Domestic / Foregin | Foregin |
Volume, Issue, Page | 17(9),pp.1844-1855 |
Author and coauthor | Otsuki, M. Gao, H. Dahlman-Wright, K. Ohlsson, C. Eguchi, N. Urade, Y. Gustafsson, J. A. |
Authorship | Lead author |
Publication date | 2003 |
Summary | Estrogens have important physiological roles in the cardiovascular system. We use DNA microarray technology to study the molecular mechanism of estrogen action in the heart and to identify novel estrogen-regulated genes. In this investigation we identify genes that are regulated by chronic estrogen treatment of mouse heart. We present our detailed characterization of one of these genes, lipocalin-type prostaglandin D synthase (L-PGDS). Northern and Western blot analysis revealed that L-PGDS was induced both by acute and chronic estrogen treatment. Northern blot analysis, using estrogen receptor (ER)-disrupted mice, suggests that L-PGDS is specifically induced by ERbeta in vivo. In further support of ERbeta-selective regulation, we identify a functional estrogen-responsive element in the L-PGDS promoter, the activity of which is up-regulated by ERbeta, but not by ERalpha. We demonstrate that a one-nucleotide change (A to C) in the L-PGDS estrogen-responsive element affects receptor selectivity. |
DOI | 10.1210/me.2003-0016 |
Document No. | 12829806 |