4.5 Article

The interleukin 6 trans-signaling increases prostaglandin E2 production in human granulosa cells

Journal

BIOLOGY OF REPRODUCTION
Volume 105, Issue 5, Pages 1189-1204

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/biolre/ioab128

Keywords

interleukin 6; IL6 trans-signaling; SOCS3; PTGS2; PGE2

Funding

  1. China Scholarship Council [201806275007]
  2. Canadian Institutes of Health Research [143317]
  3. National Natural Science Foundation of China [81701412]
  4. Nature Science Foundation of Hubei Province Grant [2018CFB491]
  5. Hubei Chenguang Talented Youth Development Foundation

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This study elucidates the molecular mechanisms by which interleukin 6 trans-signaling upregulates the expression of prostaglandin-endoperoxide 2 and increases prostaglandin E-2 production in the human ovary.
As a potent autocrine regulator, the proinflammatory cytokine interleukin 6 (IL6) is expressed in granulosa cells and is involved in the modulation of various follicular functions, including follicular development and ovulation. At present, the detailed molecular mechanisms by which IL6 regulates the event of ovulation remain to be elucidated. In the present study, primary and immortalized (SVOG) human granulosa-lutein (hGL) cells were used to investigate the effects of IL6 on the expression of prostaglandin-endoperoxide synthase 2 (PTGS2) and the subsequent synthesis of prostaglandin E-2 (PGE(2)) and to investigate the underlying molecular mechanisms. We found that instead of classic signaling, IL6/soluble form of the IL6 receptor (sIL-6Ralpha) trans-signaling induced the expression of PTGS2 and production of PGE(2) in both SVOG cells and primary hGL cells. Moreover, IL6/sIL-6Ralpha activated the phosphorylation of Janus-activated kinase 2 (JAK2) and signal transducer and activator of transcription 3 (STAT3), which in turn induced STAT3 nuclear translocation. In addition, these effects were suppressed by the addition of inhibitors (AG490 for JAK2 and C188-9 for STAT3) and by the small interfering RNA-mediated knockdown of STAT3. In addition, suppressor of cytokine signaling 3 (SOCS3) acts as a negative-feedback regulator in IL6/sIL-6Ralpha-induced cellular activities, including the activation and nuclear translocation of STAT3, upregulation of PTGS2 expression, and increase in PGE(2) production in SVOG cells. In conclusion, IL6 trans-signaling upregulates the expression of PTGS2 and increases the production of PGE(2) via the JAK2/STAT3/SOCS3 signaling pathway in hGL cells. Our findings provide insights into the molecular mechanisms by which IL6 trans-signaling may potentially modulate the event of ovulation in human ovaries. Summary sentence This is a detailed study of the underlying molecular mechanisms by which interleukin 6 trans-signaling upregulates the expression of prostaglandin-endoperoxide 2 and increases prostaglandin E-2 production in the human ovary.

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