The regulation and function of acetylated high-mobility group box 1 during implantation and decidualization
Open Access
- 25 January 2023
- journal article
- research article
- Published by Frontiers Media SA in Frontiers in Immunology
- Vol. 14, 1024706
Abstract
Introduction: High-mobility group box 1 (HMGB1) is a non-histone nuclear protein and can be extracellularly secreted to induce sterile inflammation. Although uterine deletion of HMGB1 causes implantation and decidualization defects, how secreted HMGB1 is involved in mouse early pregnancy is still unknown.Methods: Mouse models, mouse primary endometrial cells and human endometrial cell lines were used in this study. Both immunofluorescence and Western blot were performed to show the localization and relative level of HMGB1 and acetylated HMGB1, respectively. Relative mRNA levels were analyzed by real time RT-PCR.Results: The secreted HMGB1 was detected in uterine lumen fluid in mouse periimplantation uterus. There is an obvious difference for secreted HMGB1 levels in uterine fluid between day 4 of pregnancy and day 4 of pseudopregnancy, suggesting the involvement of blastocysts during HMGB1 secretion. Trypsin is clearly detected in mouse blastocyst cavity and in the supernatant of cultured blastocysts. Trypsin significantly stimulates HB-EGF production through activating PAR2 and ADAM17. Uterine injection of PAR2 inhibitor into day 4 pregnant mice significantly reduces the number of implantation sites. HB-EGF released from luminal epithelium can induce mouse in vitro decidualization. The conditioned medium collected from trypsin-treated luminal epithelium is able to induce in vitro decidualization, which is suppressed by EGFR inhibitor. Intrauterine injection of glycyrrhizin (HMGB1 inhibitor) can significantly inhibit mouse embryo implantation. We also showed that exogenous HMGB1 released from human epithelial cells are able to induce human in vitro decidualization.Conclusion: Trypsin can induce decidualization of stromal cells via PAR2-HMGB1-ADAM17-HB-EGF from luminal epithelium.Keywords
Funding Information
- National Key Research and Development Program of China
- National Natural Science Foundation of China
This publication has 54 references indexed in Scilit:
- Serine protease inhibitor 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride (AEBSF) inhibits the rat embryo implantation in vivo and interferes with cell adhesion in vitroContraception, 2011
- Ectodomain shedding of HB-EGF: A potential target for cancer therapyThe Journal of Biochemistry, 2011
- Shedding of the Mer Tyrosine Kinase Receptor Is Mediated by ADAM17 Protein through a Pathway Involving Reactive Oxygen Species, Protein Kinase Cδ, and p38 Mitogen-activated Protein Kinase (MAPK)Journal of Biological Chemistry, 2011
- Microarray assessment of the influence of the conceptus on gene expression in the mouse uterus during decidualizationReproduction, 2011
- Inflammation and pregnancy: the role of the immune system at the implantation siteAnnals of the New York Academy of Sciences, 2011
- Sterile inflammation: sensing and reacting to damageNature Reviews Immunology, 2010
- Mitochondrial Reactive Oxygen Species Mediate GPCR–induced TACE/ADAM17-dependent Transforming Growth Factor-α SheddingMolecular Biology of the Cell, 2009
- Maternal heparin-binding-EGF deficiency limits pregnancy success in miceProceedings of the National Academy of Sciences, 2007
- Mice with defects in HB-EGF ectodomain shedding show severe developmental abnormalitiesJournal of Cell Biology, 2003
- Tumor Necrosis Factor-α Converting Enzyme/ADAM 17 Mediates MUC1 SheddingJournal of Biological Chemistry, 2003