Elevated Peritoneal Fluid TNF-α Incites Ovarian Early Growth Response Factor 1 Expression and Downstream Protease Mediators: A Correlation With Ovulatory Dysfunction in Endometriosis

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Elevated peritoneal fluid TNF-α in endometriosis models correlates with increased ovarian Egr1 expression, potentially impeding ovulation through downstream protease pathways.

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The paper investigated signaling pathways linking peritoneal endometriotic lesions to ovulatory failure by profiling ovarian gene expression and focusing on how elevated peritoneal fluid TNF-α could regulate early growth response factor 1 (Egr1). Using genome-wide microarray analysis of ovarian tissue from a rat in vivo endometriosis model (Endo) versus sham controls, the authors found 22 differentially expressed genes, including Egr1, and reported that Egr1 mRNA and EGR1 protein localization differed in follicular compartments along with increased peritoneal fluid TNF-α in Endo rats. The authors propose that elevated TNF-α–driven follicular EGR1 affects downstream protease mediators implicated in impaired ovulation, and include preliminary human data showing similar EGR1 protein localization patterns in endometriosis versus non-endometriosis ovaries. A key caveat is that downstream protease pathway effects are described as preliminary/correlative rather than fully mechanistically established in the presented text. This paper is centrally about endometriosis — it examines TNF-α–EGR1 signaling in the ovary associated with ovulatory dysfunction in an endometriosis model and includes preliminary human localization data.

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Abstract

Endometriosis-associated infertility manifests itself via multiple, poorly understood mechanisms. Our goal was to characterize signaling pathways, between peritoneal endometriotic lesions and the ovary, leading to failed ovulation. Genome-wide microarray analysis comparing ovarian tissue from an in vivo endometriosis model in the rat (Endo) with controls (Sham) identified 22 differentially expressed genes, including transiently expressed early growth response factor 1 (Egr1). The Egr1 regulates gene requisites for ovulation. The Egr1 promoter is responsive to tumor necrosis factor-alpha (TNF-α) signaling. We hypothesized that altered expression of ovarian EGR1 is induced by elevated peritoneal fluid TNF-α which is upregulated by the presence of peritoneal endometriosis. Endo rats, compared to controls, had more peritoneal fluid TNF-α and quantitative, spatial differences in Egr1 mRNA and EGR1 protein localization in follicular compartments. Interactions between elevated peritoneal fluid TNF-α and overexpression of follicular Egr1/EGR1 expression may affect downstream protease pathways impeding ovulation in endometriosis. Preliminary studies identified similar patterns of EGR1 protein localization in human ovaries from women with endometriosis and compared to those without endometriosis. Similar content being viewed by others

References

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Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Birt, J.A., Nabli, H., Stilley, J.A. et al. Elevated Peritoneal Fluid TNF-α Incites Ovarian Early Growth Response Factor 1 Expression and Downstream Protease Mediators: A Correlation With Ovulatory Dysfunction in Endometriosis. Reprod. Sci. 20, 514–523 (2013). https://doi.org/10.1177/1933719113477479 Published: Issue date: DOI: https://doi.org/10.1177/1933719113477479

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mesh:D004715endometriosis

MeSH descriptors

Ascitic Fluid Early Growth Response Protein 1 Endometriosis Ovary Ovulation Peptide Hydrolases Tumor Necrosis Factor-alpha Animals Ascitic Fluid Ascitic Fluid Binding Sites Case-Control Studies Disease Models, Animal Early Growth Response Protein 1 Early Growth Response Protein 1 Endometriosis Endometriosis Endometriosis Endometriosis Female

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