Interleukin-33 regulates the endoplasmic reticulum stress of human myometrium via an influx of calcium during initiation of labor

Elife. 2022 Aug 23:11:e75072. doi: 10.7554/eLife.75072.

Abstract

Background: Inflammation is currently recognized as one of the major causes of premature delivery. As a member of the interleukin-1β (IL-1β) family, interleukin-33 (IL-33) has been shown to be involved in normal pregnancy as well as a variety of pregnancy-related disorder. This study aims to investigate the potential function of IL-33 in uterine smooth muscle cells during labor.

Methods: Myometrium samples from term pregnant (≥37 weeks gestation) women were either frozen or cells were isolated and cultured. Immunohistochemistry and western blotting were used to assess the distribution of IL-33. Cultured cells were incubated with lipopolysaccharide (LPS) to mimic inflammation as well as in the presence of 4μ8C (IRE1 inhibitor III) to block endoplasmic reticulum (ER) stress and BAPTA-AM, a calcium chelator.

Results: LPS reduced the expression of nuclear IL-33 in a time-limited manner and induced ER stress. However, knockdown of IL-33 increased LPS-induced calcium concentration, ER stress and phosphorylation of nuclear factor kappa-B (NF-κB), and P38 mitogen-activated protein kinase (P38 MAPK). In addition, siRNA IL-33 further stimulates LPS enhanced cyclooxygenase-2 (COX-2) expression via NF-κB and p38 pathways. IL-33 expression was decreased in the nucleus with the onset of labor. LPS-induced ER stress and increased expression of the labor-associated gene, COX-2, as well as IL-6 and IL-8 in cultured myometrial cells. IL-33 also increased COX-2 expression, but after it was knocked down, the stimulating effect of LPS on calcium was enhanced. 4μ8C also inhibited the expression of COX-2 markedly. The expression of calcium channels on the membrane and intracellular free calcium ion were both increased which was accompanied by phosphorylated NF-κB and p38.

Conclusions: These data suggest that IL-33 may be involved in the initiation of labor by leading to stress of the ER via an influx of calcium ions in human uterine smooth muscle cells.

Funding: This study was supported by grants from the National Natural Science Foundation of China (No. 81300507).

Keywords: calcium channels; cell biology; human; inflammation; interleukin-33; medicine; myometrium; preterm labor; stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism
  • Cells, Cultured
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Endoplasmic Reticulum Stress
  • Female
  • Humans
  • Inflammation / metabolism
  • Interleukin-33 / metabolism*
  • Lipopolysaccharides / metabolism
  • Myometrium* / metabolism
  • NF-kappa B* / metabolism
  • Pregnancy
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • IL33 protein, human
  • Interleukin-33
  • Lipopolysaccharides
  • NF-kappa B
  • Cyclooxygenase 2
  • p38 Mitogen-Activated Protein Kinases
  • Calcium

Grants and funding

The funders had no role in study design, data collection, and interpretation, or the decision to submit the work for publication.