Dose–response effect of interleukin (IL)-1β, tumour necrosis factor (TNF)-α, and interferon-γ on the in vitro production of epithelial neutrophil activating peptide-78 (ENA-78), IL-8, and IL-6 by human endometrial stromal cells

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IL-1β and TNF-α dose-dependently stimulated endometrial stromal cell production of ENA-78, IL-8, and IL-6, while interferon-γ stimulated IL-6 and inhibited IL-8.

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The study examined how different doses of IL-1β, TNF-α, and interferon-γ affect in vitro production of the neutrophil-activating chemokine ENA-78 and the cytokines IL-8 and IL-6 by human endometrial stromal cells. Stromal cells derived from eutopic endometrium of seven cycling endometriosis-free women were isolated and cultured (including monolayers) and then exposed to IL-1β (0.08–50 ng/mL), TNF-α, and interferon-γ (20–500 ng/mL), with ENA-78, IL-8, and IL-6 release measured. IL-1β increased all three mediators dose-dependently but showed decreased IL-8 and IL-6 release at the highest IL-1β dose tested, while TNF-α produced a plateau effect across a dose range and interferon-γ had opposite effects by inhibiting IL-8 above 20 ng/mL while stimulating IL-6 and largely leaving ENA-78 unaffected. Limitations include small sample size (n=7) and reliance on eutopic, endometriosis-free stromal cells rather than endometriotic tissue. This paper is centrally about endometriosis in its use of IL-8 and ENA-78 biology, explicitly noting that IL-8 and ENA-78 are increased in endometriosis peritoneal fluid and framing stromal cytokine regulation relevant to endometriosis.

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Abstract

PurposeThe production of epithelial neutrophil activating peptide-78 (NA-78) and the interleukins IL-8 and IL-6 by endometrial stromal cells is stimulated by pro-inflammatory interleukin-1 (IL-1) and tumour necrosis factor-α (TNF-α). IL-8 is suggested to play a role in the pathogenesis of endometriosis, and in these women the peritoneal fluid concentrations of ENA-78 and IL-8 are increased. TNF-α has been tested together with interferon-γ because of their cooperative stimulation of IL-6. The release of IL-8, however, is inhibited with increasing interferon levels. The aim of the study was the analysis of the production of ENA-78, IL-6 and IL-8 by cultured human endometrial stromal cells in the presence of varying concentrations of IL-1β, TNF-α, and interferon-γ.MethodsEutopic endometrial tissue was obtained from seven cycling, endometriosis-free women undergoing laparoscopy for reasons of infertility or pain. The release of ENA-78, IL-8 and IL-6 by the isolated and monolayer cultured stromal cell fraction in the presence of IL-1β (0.08 to 50 ng/mL), TNF-α, and interferon-γ (both 20 to 500 ng/mL) was determined.ResultsIL-1β stimulated the production of IL-8, IL-6, and ENA-78 dose dependently from 0.08 to 2.0 ng/mL (ENA-78) or to 10 ng/mL (IL-8, IL-6); at 50 ng/mL a decrease in release was observed for IL-8 and IL-6. TNF-α stimulation yielded a plateau between 20 and 100 ng/mL. Interferon-γ stimulated IL-6 and inhibited IL-8 production above 20 ng/mL. ENA-78 release was largely unaffected by interferon-γ.ConclusionsIL-1β and TNF-α stimulate stromal cytokine production cumulatively with different dose-response curves. The presence of interferon-γ has opposite effects on IL-8 and IL-6. TNF-α and interferon-γ should be investigated separately in future in vitro studies with endometrial cells and explants.
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Abstract

Purpose The production of epithelial neutrophil activating peptide-78 (NA-78) and the interleukins IL-8 and IL-6 by endometrial stromal cells is stimulated by pro-inflammatory interleukin-1 (IL-1) and tumour necrosis factor-α (TNF-α). IL-8 is suggested to play a role in the pathogenesis of endometriosis, and in these women the peritoneal fluid concentrations of ENA-78 and IL-8 are increased. TNF-α has been tested together with interferon-γ because of their cooperative stimulation of IL-6. The release of IL-8, however, is inhibited with increasing interferon levels. The aim of the study was the analysis of the production of ENA-78, IL-6 and IL-8 by cultured human endometrial stromal cells in the presence of varying concentrations of IL-1β, TNF-α, and interferon-γ.

Methods

Eutopic endometrial tissue was obtained from seven cycling, endometriosis-free women undergoing laparoscopy for reasons of infertility or pain. The release of ENA-78, IL-8 and IL-6 by the isolated and monolayer cultured stromal cell fraction in the presence of IL-1β (0.08 to 50 ng/mL), TNF-α, and interferon-γ (both 20 to 500 ng/mL) was determined.

Results

IL-1β stimulated the production of IL-8, IL-6, and ENA-78 dose dependently from 0.08 to 2.0 ng/mL (ENA-78) or to 10 ng/mL (IL-8, IL-6); at 50 ng/mL a decrease in release was observed for IL-8 and IL-6. TNF-α stimulation yielded a plateau between 20 and 100 ng/mL. Interferon-γ stimulated IL-6 and inhibited IL-8 production above 20 ng/mL. ENA-78 release was largely unaffected by interferon-γ.

Conclusions

IL-1β and TNF-α stimulate stromal cytokine production cumulatively with different dose–response curves. The presence of interferon-γ has opposite effects on IL-8 and IL-6. TNF-α and interferon-γ should be investigated separately in future in vitro studies with endometrial cells and explants. Similar content being viewed by others

References

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Arch Gynecol Obstet 283, 1291–1296 (2011). https://doi.org/10.1007/s00404-010-1520-3 Received: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s00404-010-1520-3

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MeSH descriptors

Chemokine CXCL5 Endometrium Endometrium Interferon-gamma Interleukin-1beta Interleukin-6 Interleukin-8 Stromal Cells Stromal Cells Tumor Necrosis Factor-alpha Cells, Cultured Chemokine CXCL5 Dose-Response Relationship, Drug Endometrium Endometrium Female Humans Interferon-gamma Interleukin-1beta Interleukin-6

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