Dysregulated cannabinoid signaling disrupts uterine receptivity for embryo implantation

被引:153
作者
Paria, BC
Song, H
Wang, X
Schmid, PC
Krebsbach, RJ
Schmid, HHO
Bonner, TI
Zimmer, A
Dey, SK
机构
[1] Univ Kansas, Med Ctr, Ralph L Smith Res Ctr, Dept Mol & Intergrat Physiol, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Pediat, Kansas City, KS 66160 USA
[3] Univ Minnesota, Hormel Inst, Austin, MN 55912 USA
[4] NIMH, Genet Lab, Bethesda, MD 20892 USA
[5] Univ Bonn, Psychiat Clin, Mol Neurobiol Lab, D-53105 Bonn, Germany
关键词
D O I
10.1074/jbc.M100679200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanisms by which synchronized embryonic development to the blastocyst stage, preparation of the uterus for the receptive state, and reciprocal embryo-uterine interactions for implantation are coordinated are still unclear. We show in this study that preimplantation embryo development became asynchronous in mice that are deficient in brain-type (CB1) and/or spleen-type (CB2) cannabinoid receptor genes. Furthermore, whereas the levels of uterine anandamide (endocannabinoid) and blastocyst CB1 are coordinately down-regulated with the onset of uterine receptivity and blastocyst activation prior to implantation, these levels remained high in the nonreceptive uterus and in dormant blastocysts during delayed implantation and in pregnant, leukemia inhibitory factor (LIF)-deficient mice with implantation failure. These results suggest that a tight regulation of endocannabinoid signaling is important for synchronizing embryo development with uterine receptivity for implantation. Indeed this is consistent with our finding that while an experimentally induced, sustained level of an exogenously administered, natural cannabinoid inhibited implantation in wild-type mice, it failed to do so in CB1(-/-)/CB2(-/-) double mutant mice. The present study is clinically important because of the widely debated medicinal use of cannabinoids and their reported adverse effects on pregnancy.
引用
收藏
页码:20523 / 20528
页数:6
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