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In the mouse, prostaglandin D2 signalling protects the endometrium against adenomyosis

Title: In the mouse, prostaglandin D2 signalling protects the endometrium against adenomyosis
Authors: Philibert, Pascal; Déjardin, Stéphanie; Pirot, Nelly; Pruvost, Alain; Nguyen, Anvi Laetitia; Bernex, Florence; Poulat, Francis; Boizet-Bonhoure, Brigitte
Contributors: Institut de génétique humaine (IGH); Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS); Centre Hospitalier Universitaire de Nîmes (CHU Nîmes); Institut de Recherche en Cancérologie de Montpellier (IRCM - U1194 Inserm - UM); CRLCC Val d'Aurelle - Paul Lamarque-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM); BioCampus (BCM); Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS); Médicaments et Technologies pour la Santé (MTS); Université Paris-Saclay-Institut des Sciences du Vivant Frédéric JOLIOT (JOLIOT); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE); ANR-11-INBS-0010,METABOHUB,Développement d'une infrastructure française distribuée pour la métabolomique dédiée à l'innovation(2011)
Source: ISSN: 1360-9947.
Publisher Information: CCSD; Oxford University Press (OUP)
Publication Year: 2021
Collection: Inserm: HAL (Institut national de la santé et de la recherche médicale)
Subject Terms: prostaglandin E2; mouse model; prostaglandin D2; endometrium; adenomyosis; [SDV.BA]Life Sciences [q-bio]/Animal biology
Description: International audience ; Adenomyosis is characterised by epithelial gland and mesenchymal stroma invasion of the uterine myometrium. Adenomyosis is an oestrogen-dependent gynaecological disease in which a number of factors, such as inflammatory molecules, prostaglandins (PGs), angiogenic factors, cell proliferation and extracellular matrix remodelling proteins, also play a role as key disease mediators. In this study, we used mice lacking both lipocalin and hematopoietic-PG D synthase (L- and H-Pgds) genes in which PGD2 is not produced to elucidate PGD2 roles in the uterus. Gene expression studied by real-time PCR and hormone dosages performed by ELISA or liquid chromatography tandem mass spectroscopy in mouse uterus samples showed that components of the PGD2 signalling pathway, both PGDS and PGD2-receptors, are expressed in the mouse endometrium throughout the oestrus cycle with some differences among uterine compartments. We showed that PGE2 production and the steroidogenic pathway are dysregulated in the absence of PGD2. Histological analysis of L/H-Pgds−/− uteri, and immunohistochemistry and immunofluorescence analyses of proliferation (Ki67), endothelial cell (CD31), epithelial cell (pan-cytokeratin), myofibroblast (α-SMA) and mesenchymal cell (vimentin) markers, identify that 6-month-old L/H-Pgds−/− animals developed adenomyotic lesions, and that disease severity increased with age. In conclusion, this study suggests that the PGD2 pathway has major roles in the uterus by protecting the endometrium against adenomyosis development. Additional experiments, using for instance transcriptomic approaches, are necessary to fully determine the molecular mechanisms that lead to adenomyosis in L/H-Pgds−/− mice and to confirm whether this strain is an appropriate model for studying the human disease.
Document Type: article in journal/newspaper
Language: English
Relation: WOS: 000697163300006
DOI: 10.1093/molehr/gaab029
Availability: https://hal.science/hal-03436852; https://hal.science/hal-03436852v1/document; https://hal.science/hal-03436852v1/file/Philibert%20MolHuman%20Reproduction%202021%20gaab029%20.pdf; https://doi.org/10.1093/molehr/gaab029
Rights: https://about.hal.science/hal-authorisation-v1/ ; info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.731AF444
Database: BASE