Labour-associated increase in interleukin-1 alpha release in vitro by human gestational tissues

N Laham1, S P Brennecke, K Bendtzen

  • 1Department of Perinatal Medicine, Royal Women's Hospital, Carlton, Victoria, Australia.

Insights

Interleukin-1 alpha (IL-1 alpha) release from fetal membranes increases during term labor, independent of bacterial endotoxin. Placental IL-1 alpha also rises with labor and responds to lipopolysaccharide (LPS).

Area of Science:

  • Reproductive Biology
  • Immunology
  • Maternal-Fetal Medicine

Background:

  • Interleukin-1 alpha (IL-1 alpha) is a key inflammatory mediator.
  • Its role in human term labor onset and regulation by bacterial endotoxins is not fully understood.

Purpose of the Study:

  • To investigate IL-1 alpha concentration and release during human term labor.
  • To examine the regulation of IL-1 alpha release from gestational tissues by bacterial endotoxin (lipopolysaccharide, LPS).

Main Methods:

  • Quantification of immunoreactive IL-1 alpha in maternal plasma, amniotic fluid, and explants of amniotic, choriodecidual, and placental tissues.
  • Assessment of IL-1 alpha release from tissue explants in response to LPS over time and varying concentrations.

Main Results:

  • Maternal plasma and amniotic fluid IL-1 alpha levels did not significantly change with labor onset.
  • IL-1 alpha was released from amniotic and choriodecidual explants specifically with term labor onset and delivery.
  • Placental IL-1 alpha release significantly increased with term labor onset and delivery.
  • LPS significantly increased IL-1 alpha release only from placental explants.

Conclusions:

  • IL-1 alpha release from human gestational tissues is differentially regulated in association with labor and LPS treatment.
  • The labor-associated increase in IL-1 alpha release from fetal membranes appears independent of bacterial endotoxin exposure.