Macrophages are a source of IL-17 in the human placenta

Am J Reprod Immunol. 2018 Oct;80(4):e13016. doi: 10.1111/aji.13016. Epub 2018 Jun 29.

Abstract

Problem: To determine if placental macrophages (Hofbauer cells) can synthesize and secrete cytokines of the IL-17 family throughout pregnancy and to reveal the patterns of cytokine expression in early and late gestation.

Methods of study: Macrophages were isolated from the first-trimester and term placental villous tissues from normal pregnancies. Basal and stimulated intracellular production of IL-17A, IL-17E, IL-17F as well as IL-17A secretion was quantified by flow cytometry and cytometric bead array, respectively. The expression of IL-17 and IL-23 receptors was determined on the surface of the placental macrophages by flow cytometry after antibody staining.

Results: In early and late gestation, a substantial proportion of the placental macrophages synthesized IL-17A and IL-17F, but not IL-17E, as determined by intracellular staining of the cytokines. Neither the intracellular production nor the secretion of IL-17 was significantly affected by LPS stimulation and spontaneous labour. The level of secretion decreased slightly but significantly at term. The IL-23 receptor was absent on the surface of cells, whereas variable expression of the IL-17 receptor was observed.

Conclusion: Placental macrophages constitutively produced IL-17 at different gestational ages and represent thus a source of this cytokine in the human placenta. Patterns of the cytokine and receptor expression suggest that this cell population may participate in non-immune processes and contribute to the regulation of placental development and function.

Keywords: IL-17; LPS; first trimester; macrophages; placenta; term pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Chorionic Villi / immunology*
  • Female
  • Humans
  • Interleukin-17 / metabolism*
  • Macrophages / immunology*
  • Pregnancy
  • Pregnancy Trimester, First
  • Receptors, Interleukin / metabolism*

Substances

  • IL17A protein, human
  • IL17F protein, human
  • IL23R protein, human
  • IL25 protein, human
  • Interleukin-17
  • Receptors, Interleukin