Lysophosphatidic receptor, LPA3, is positively and negatively regulated by progesterone and estrogen in the mouse uterus

被引:54
作者
Hama, Kotaro
Aoki, Junken
Bandoh, Koji
Inoue, Asuka
Endo, Tomoko
Amano, Tomokazu
Suzuki, Hiroshi
Arai, Hiroyuki
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Dev & Med Technol, Bunkyo Ku, Tokyo 1130033, Japan
[3] Obihiro Univ Agr & Vet Med, Obihiro, Hokkaido 0808555, Japan
关键词
implantation; LPA(3); lysophosphatidic acid; progesterone; estrogen;
D O I
10.1016/j.lfs.2006.06.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Reciprocal interactions between blastocysts and receptive uteri are essential for successful implantation. This process is regulated by the timely interplay of two ovarian hormones, progesterone and estrogen. However, the molecular targets of these hormones are largely unknown. We showed recently that a small bioactive lysophospholipid, lysophosphatidic acid, plays a pivotal role in the establishment of implantation via its cellular receptor, LPA(3). Here we demonstrate that LPA(3) expression is positively and negatively regulated by steroid hormones in mouse uteri. The LPA(3) mRNA level in the uteri increased during early pseudopregnancy, peaking around 3.5 days post coitus (3.5 d.p.c.), then, decreased to the basal level on 4.5 d.p.c. LPA(3) expression remained at a low level in ovariectomized mice, and administration of progesterone to ovariectomized mice up-regulated LPA(3) mRNA expression. In addition, simultaneous administration of estrogen counteracted the effect of progesterone. These results show that progesterone and estrogen cooperatively regulate LPA(3) expression, thereby contributing to the receptivity of uteri during early pregnancy. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1736 / 1740
页数:5
相关论文
共 22 条
[1]
Characterization of a novel subtype of human G protein-coupled receptor for lysophosphatidic acid [J].
An, SZ ;
Bleu, T ;
Hallmark, OG ;
Goetzl, EJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (14) :7906-7910
[2]
ARDELL SE, 2006, TRENDS MOL MED, V12, P65
[3]
Molecular cloning and characterization of a novel human G-protein-coupled receptor, EDG7, for lysophosphatidic acid [J].
Bandoh, K ;
Aoki, J ;
Hosono, H ;
Kobayashi, S ;
Kobayashi, T ;
Murakami-Murofushi, K ;
Tsujimoto, M ;
Arai, H ;
Inoue, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) :27776-27785
[4]
Embryo implantation [J].
Carson, DD ;
Bagchi, I ;
Dey, SK ;
Enders, AC ;
Fazleabas, AT ;
Lessey, BA ;
Yoshinaga, K .
DEVELOPMENTAL BIOLOGY, 2000, 223 (02) :217-237
[5]
Lysophosphatidic acid receptors [J].
Contos, JJA ;
Ishii, I ;
Chun, J .
MOLECULAR PHARMACOLOGY, 2000, 58 (06) :1188-1196
[6]
Requirement for the IpA1 lysophosphatidic acid receptor gene in normal suckling behavior [J].
Contos, JJA ;
Fukushima, N ;
Weiner, JA ;
Kaushal, D ;
Chun, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (24) :13384-13389
[7]
Characterization of lpa2 (Edg4) and lpa1/lpa2 (Edg2/Edg4) lysophosphatidic acid receptor knockout mice:: Signaling deficits without obvious phenotypic abnormality attributable to lpa2 [J].
Contos, JJA ;
Ishii, I ;
Fukushima, N ;
Kingsbury, MA ;
Ye, XQ ;
Kawamura, S ;
Brown, JH ;
Chun, J .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (19) :6921-6929
[8]
Molecular cues to implantation [J].
Dey, SK ;
Lim, H ;
Das, SK ;
Reese, J ;
Paria, BC ;
Daikoku, T ;
Wang, HB .
ENDOCRINE REVIEWS, 2004, 25 (03) :341-373
[9]
EMBRYONIC SIGNALS IN PREGNANCY [J].
DEY, SK ;
JOHNSON, DC .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1986, 476 :49-62
[10]
Lysophosphatidic acid and autotaxin stimulate cell motility of neoplastic and non-neoplastic cells through LPA1 [J].
Hama, K ;
Aoki, J ;
Fukaya, M ;
Kishi, Y ;
Sakai, T ;
Suzuki, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (17) :17634-17639