Augmented epithelial multidrug resistance-associated protein 4 expression in peritoneal endometriosis: regulation by lipoxin A(4).

Détails

ID Serval
serval:BIB_2978E38F179E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Augmented epithelial multidrug resistance-associated protein 4 expression in peritoneal endometriosis: regulation by lipoxin A(4).
Périodique
Fertility and Sterility
Auteur⸱e⸱s
Gori I., Rodriguez Y., Pellegrini C., Achtari C., Hornung D., Chardonnens E., Wunder D., Fiche M., Canny G.O.
ISSN
1556-5653 (Electronic)
ISSN-L
0015-0282
Statut éditorial
Publié
Date de publication
2013
Peer-reviewed
Oui
Volume
99
Numéro
7
Pages
1965-73.e2
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
OBJECTIVE: To compare the expression of the prostaglandin (PG) E(2) transporter multidrug resistance-associated protein 4 (MRP4) in eutopic and ectopic endometrial tissue from endometriosis patients with that of control subjects and to examine whether MRP4 is regulated by the antiinflammatory lipid lipoxin A(4) (LXA(4)) in endometriotic epithelial cells.
DESIGN: Molecular analysis in human samples and a cell line.
SETTING: Two university hospitals and a private clinic.
PATIENT(S): A total of 59 endometriosis patients and 32 age- and body mass index-matched control subjects undergoing laparoscopy or hysterectomy.
INTERVENTION(S): Normal, eutopic, and ectopic endometrial biopsies as well as peritoneal fluid were obtained during surgery performed during the proliferative phase of the menstrual cycle. 12Z endometriotic epithelial cells were used for in vitro mechanistic studies.
MAIN OUTCOME MEASURE(S): Tissue MRP4 mRNA levels were quantified by quantitative reverse-transcription polymerase chain reaction (qRT-PCR), and localization was analyzed with the use of immunohistochemistry. Cellular MRP4 mRNA and protein were quantified by qRT-PCR and Western blot, respectively. PGE(2) was measured in peritoneal fluid and cell supernatants using an enzyme immunoassay (EIA).
RESULT(S): MRP4 was expressed in eutopic and ectopic endometrium, where it was overexpressed in peritoneal lesions and localized in the cytoplasm of glandular epithelial cells. LXA(4) attenuated MRP4 mRNA and protein levels in endometriotic epithelial cells in a dose-dependent manner, while not affecting the expression of enzymes involved in PGE(2) metabolism. Investigations employing receptor antagonists and small interfering RNA revealed that this occurred through estrogen receptor α. Accordingly, LXA(4) treatment inhibited extracellular PGE(2) release.
CONCLUSION(S): We report for the first time that MRP4 is expressed in human endometrium, elevated in peritoneal endometriosis, and modulated by LXA(4) in endometriotic epithelial cells.
Mots-clé
Adult, Ascitic Fluid/metabolism, Biopsy, Blotting, Western, Case-Control Studies, Cell Line, Dinoprostone/metabolism, Endometriosis/genetics, Endometriosis/metabolism, Endometrium/drug effects, Endometrium/metabolism, Epithelial Cells/drug effects, Epithelial Cells/metabolism, Estrogen Antagonists/pharmacology, Estrogen Receptor alpha/antagonists & inhibitors, Estrogen Receptor alpha/genetics, Female, Humans, Hysterectomy, Immunoenzyme Techniques, Immunohistochemistry, Laparoscopy, Lipoxins/metabolism, Middle Aged, Multidrug Resistance-Associated Proteins/genetics, Multidrug Resistance-Associated Proteins/metabolism, Peritoneal Diseases/genetics, Peritoneal Diseases/metabolism, RNA Interference, RNA, Messenger/metabolism, Reverse Transcriptase Polymerase Chain Reaction, Transfection, Up-Regulation, Young Adult
Pubmed
Web of science
Création de la notice
06/06/2013 14:16
Dernière modification de la notice
20/08/2019 13:09
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