Role of estrogen receptor signaling required for endometriosis-like lesion establishment in a mouse model

Burns KA, Katherine A. Burns, Rodriguez KF, Karina F. Rodriguez, Sylvia C. Hewitt, Kyathanahalli S. Janardhan, Janardhan KS, Steven L. Young, Kenneth S. Korach
Endocrinology · 2012 · vol. 153(8) , pp. 3960–3971 · doi:10.1210/en.2012-1294 · PMID:22700766 · PMC3404357 · W2082998009
Lab / animal OA: bronze CC0 ⤵ 105 in-corpus citations
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Endometriosis-like lesions in mice required estrogen receptor alpha signaling for establishment, growth, and response to estradiol, with lesions lacking ERα showing increased inflammation but reduced distal spread and proliferation.

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Abstract

Endometriosis results from ectopic invasion of endometrial tissue within the peritoneal cavity. Aberrant levels of the estrogen receptor (ER), ERα and ERβ, and higher incidence of autoimmune disorders are observed in women with endometriosis. An immunocompetent mouse model of endometriosis was used in which minced uterine tissue from a donor was dispersed into the peritoneal cavity of a recipient. Wild-type (WT), ERα-knockout (αERKO), and βERKO mice were donors or recipients to investigate the roles of ERα, ERβ, and estradiol-mediated signaling on endometriosis-like disease. Mice were treated with vehicle or estradiol, and resulting location, number, and size of endometriosis-like lesions were assessed. In comparison with WT lesions in WT hosts, αERKO lesions in WT hosts were smaller and fewer in number. The effect of ER status and estradiol treatment on nuclear receptor status, proliferation, organization, and inflammation within lesions were examined. αERKO lesions in WT hosts did not form distal to the incision site, respond to estradiol, or proliferate but did have increased inflammation. WT lesions in αERKO hosts did respond to estradiol, proliferate, and show decreased inflammation with treatment, but surprisingly, progesterone receptor expression and localization remained unchanged. Only minor differences were observed between WT lesions in βERKO hosts and βERKO lesions in WT hosts, demonstrating the estradiol-mediated signaling responses are predominately through ERα. In sum, these results suggest ER in both endometriosis-like lesions and their environment influence lesion characteristics, and understanding these interactions may play a critical role in elucidating this enigmatic disease.

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Condition tags

endometriosis

MeSH descriptors

Disease Models, Animal Disease Models, Animal Endometriosis Receptors, Estrogen Animals Animals Endometriosis Endometriosis Endometriosis Female Female Mice Mice Mice, Knockout Mice, Knockout Receptors, Estrogen Receptors, Estrogen Receptors, Estrogen

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References (74)

Cited by (50)

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