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Agrin pathway is controlled by leukemia inhibitory factor (LIF) in murine implantation.
Full Abstract
Agrin is the heparan sulfate proteoglycan (HSPG) that is well known as the molecule that aggregates acetylcholine receptor (AChR) through muscle specific kinase (MuSK) and rapsyn at neuromuscular junctions. HSPGs are spatiotemporally expressed in embryonic and maternal tissues during implantation. The present study examined the role of agrin in the mouse embryo using leukemia inhibitory factor (LIF)-deficient mice, which show complete sterility. Agrin was detected widely in the cytoplasm of uterine luminal epithelial cells at the third day of pregnancy (Day 3) and Day 4. At Day 5, agrin moved to the apical surface of the luminal epithelium. This migration was not found in LIF-deficient mice. AChR was also found in the apical surface of the uterine epithelium at Day 4 and Day 5 in normal mice. LIF-deficient mice did not show this pattern of expression. Only nAChR b1 subunit mRNA was increased at Day 5 in normal mice. Furthermore, acetylcholinesterase was active in the uterine stroma of normal mice throughout the implantation period and was exclusively active in the uterine epithelium at Day 4. Taken together, agrin signaling was activated in the uterus during embryo implantation in the mice. Here, we suggest that the agrin pathway is involved in closure of the uterine epithelium toward placentation.
Author information
Author/s: Terakawa, Jumpei (J); Hondo, Eiichi (E); Sugiyama, Makoto (M); Wakitani, Shoichi (S); Stewart, Colin L (CL); Kiso, Yasuo (Y);
Affiliation: Department of Veterinary Anatomy, Faculty of Agriculture, Yamaguchi University.
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: The Journal of reproduction and development (J Reprod Dev), published in Japan. (Language: eng)
Reference: 2009-Jun; vol 55 (issue 3) : pp 293-8
Dates: Created 2009/07/02; Completed 2009/08/12;
PMID: 19325217, status: MEDLINE (last retrieval date: 8/21/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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