A novel mouse model of endometriosis mimics human phenotype and reveals insights into the inflammatory contribution of shed endometrium

Erin Greaves, Fiona L. Cousins, Alison Murray, Murray A, Arantza Esnal‐Zufiaurre, Arantza Esnal-Zufiaurre, Esnal-Zufiurre A, Fassbender A, Amelie Fassbender, Andrew W. Horne, Philippa T. K. Saunders
The American Journal of Pathology · 2014 · vol. 184(7) , pp. 1930–1939 · doi:10.1016/j.ajpath.2014.03.011 · PMID:24910298 · PMC4076466 · W2053121468
Lab / animal OA: bronze CC0 ⤵ 146 in-corpus citations
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This study developed a novel mouse model of endometriosis that successfully mimics human disease characteristics and provides insights into the inflammatory role of shed endometrial tissue.

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Abstract

Endometriosis is an estrogen-dependent inflammatory disorder characterized by the presence of endometrial tissue outside the uterine cavity. Patients experience chronic pelvic pain and infertility, with the most likely origin of the tissue deposits (lesions) being endometrial fragments shed at menses. Menstruation is an inflammatory process associated with a dramatic increase in inflammatory mediators and tissue-resident immune cells. In the present study, we developed and validated a mouse model of endometriosis using syngeneic menstrual endometrial tissue introduced into the peritoneum of immunocompetent mice. We demonstrate the establishment of endometriotic lesions that exhibit similarities to those recovered from patients undergoing laparoscopy. Specifically, in both cases, lesions had epithelial (cytokeratin(+)) and stromal (vimentin/CD10(+)) cell compartments with a well-developed vasculature (CD31(+) endothelial cells). Expression of estrogen receptor β was increased in lesions compared with the peritoneum or eutopic endometrium. By performing experiments using mice with green fluorescent protein-labeled macrophages (MacGreen) in reciprocal transfers with wild-type mice, we obtained evidence that macrophages present in the peritoneum and in menses endometrium can contribute to the inflammatory microenvironment of the lesions. In summary, we developed a mouse model of endometriosis that exhibits similarities to human peritoneal lesions with respect to estrogen receptor expression, inflammation, and macrophage infiltration, providing an opportunity for further studies and the possible identification of novel therapies for this perplexing disorder.

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Condition tags

endometriosis

MeSH descriptors

Disease Models, Animal Disease Models, Animal Endometriosis Endometrium Inflammation Adolescent Adolescent Adult Adult Animals Animals Endometriosis Endometriosis Endometrium Endometrium Estrogen Receptor alpha Estrogen Receptor alpha Estrogen Receptor alpha Female Female

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (51)

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