Follistatin Is Induced by IL-1β and TNF-α in Stromal Cells From Endometrioma

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Interleukin 1β and tumor necrosis factor-α induced follistatin mRNA and protein in endometrioma stromal cells, while cystic fluid showed predominant activin activity despite follistatin presence.

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The study examined how follistatin, an activin-binding protein, is regulated in endometriosis by analyzing endometrioma stromal cells from 9 patients and measuring activin-A and follistatin in endometrioma cystic fluid from 8 patients. In cultured endometrioma stromal cells, IL-1β and TNF-α induced follistatin mRNA and protein, and activin activity in cystic fluid was confirmed by a bioassay, despite follistatin being detectable by ELISA. The mean cystic fluid activin-A and follistatin concentrations were 36.8 ng/mL and 4.0 ng/mL, respectively, and activin activity was reported to be predominant in vivo. The paper is limited by using a small patient sample and by focusing on stromal-cell cytokine regulation without detailing downstream functional consequences. This paper is centrally about endometriosis—specifically the cytokine (IL-1β, TNF-α) induction of follistatin in stromal cells from ovarian endometrioma and the balance between follistatin and activin activity in endometrioma cystic fluid.

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Abstract

The aim of this study is to examine the regulation of follistatin, an activin-binding protein, in endometriosis. Endometrioma stromal cells (EoSCs) were obtained from 9 patients undergoing laparoscopy of the ovarian endometrioma. In cultured EoSCs, interleukin 1β (IL-1β) and tumor necrosis factor-α (TNF-α), which could induce activin-A, also induced follistatin messenger RNA (mRNA) and protein. The cystic fluid of endometrioma from 8 patients was obtained to measure the concentration of activin-A and follistatin by enzyme-linked immunosorbent assay (ELISA). Also, activin activity in the fluid was examined by erythroid differentiation assay using mouse erythroleukemia F5-5.fl cells. In the cystic fluid of endometrioma, the mean values of activin-A and follistatin concentration were 36.8 ng/mL and 4.0 ng/mL, respectively. In a bioassay, all 8 samples exhibited activin activity, which was equivalent to recombinant activin-A activity of 12.8 ± 1.4 ng/mL. Although follistatin was present in the cystic fluid of endometrioma, the activity of activin, which is an exacerbation factor of endometriosis, was predominant in vivo.
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Abstract

The aim of this study is to examine the regulation of follistatin, an activin-binding protein, in endometriosis. Endometrioma stromal cells (EoSCs) were obtained from 9 patients undergoing laparoscopy of the ovarian endometrioma. In cultured EoSCs, interleukin 1β (IL-1β) and tumor necrosis factor-α (TNF-α), which could induce activin-A, also induced follistatin messenger RNA (mRNA) and protein. The cystic fluid of endometrioma from 8 patients was obtained to measure the concentration of activin-A and follistatin by enzyme-linked immunosorbent assay (ELISA). Also, activin activity in the fluid was examined by erythroid differentiation assay using mouse erythroleukemia F5-5.fl cells. In the cystic fluid of endometrioma, the mean values of activin-A and follistatin concentration were 36.8 ng/mL and 4.0 ng/mL, respectively. In a bioassay, all 8 samples exhibited activin activity, which was equivalent to recombinant activin-A activity of 12.8 ± 1.4 ng/mL. Although follistatin was present in the cystic fluid of endometrioma, the activity of activin, which is an exacerbation factor of endometriosis, was predominant in vivo. Similar content being viewed by others

References

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endometriosisendometrioma

MeSH descriptors

Endometriosis Follistatin Interleukin-1beta Stromal Cells Tumor Necrosis Factor-alpha Activins Activins Animals Cell Line Endometriosis Enzyme-Linked Immunosorbent Assay Female Follistatin Follistatin Humans Interleukin-1beta Mice Real-Time Polymerase Chain Reaction Recombinant Proteins Recombinant Proteins

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