Synergistic effect of interleukin (IL)-1alpha and ceramide analogue on the production of IL-6, IL-8, and macrophage colony-stimulating factor by endometrial stromal cells

Fertil Steril. 2004 Oct:82 Suppl 3:1043-7. doi: 10.1016/j.fertnstert.2004.05.071.

Abstract

Objective: To measure the level of interleukin 6 (IL-6), IL-8, and macrophage colony-stimulating factor (M-CSF) induced by IL-1alpha in endometrial stromal cells (ESC) following treatment with ceramide analogues.

Design: The effects of IL-1alpha, IL-1 receptor antagonist (IL-1RA), C2-ceramide, and C6-ceramide on the production of IL-6, IL-8, and M-CSF by ESC.

Setting: Research laboratory at Oita University Medical School.

Patient(s): Eleven premenopausal women who had undergone hysterectomies for subserous myoma provided endometrial specimens in the secretory phase.

Intervention(s): The ESC were incubated for 24 hours with IL-1alpha, IL-1RA, C2-ceramide, and C6-ceramide.

Main outcome measure(s): The levels of IL-6, IL-8, and M-CSF in the culture media were measured via enzyme-linked immunoabsorbent assay.

Result(s): : Following stimulation by IL-1alpha, the production of IL-6, IL-8, and M-CSF showed a statistically significant increase, and they were suppressed by IL-1RA in a dose-dependent manner. Production of IL-6, IL-8, and M-CSF was not statistically significantly increased by IL-1alpha plus C2-ceramide as compared with IL-1alpha alone. Production of both IL-8 and M-CSF was statistically significantly increased by IL-1alpha plus C6-ceramide as compared with IL-1alpha alone; however, IL-6 production was not increased.

Conclusion(s): The results suggest that IL-1alpha stimulates the production of IL-8 and M-CSF by a mechanism that involves the sphingomyelin-ceramide system. Ceramide may be important in increasing the production of IL-8 and M-CSF in the human endometrium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cells, Cultured
  • Ceramides / pharmacology*
  • Endometrium / cytology
  • Endometrium / metabolism*
  • Female
  • Humans
  • Interleukin 1 Receptor Antagonist Protein
  • Interleukin-1 / pharmacology*
  • Interleukin-6 / biosynthesis*
  • Interleukin-8 / biosynthesis*
  • Macrophage Colony-Stimulating Factor / biosynthesis*
  • Sialoglycoproteins / pharmacology
  • Sphingosine / analogs & derivatives*
  • Sphingosine / pharmacology*
  • Stromal Cells / metabolism

Substances

  • Ceramides
  • IL1RN protein, human
  • Interleukin 1 Receptor Antagonist Protein
  • Interleukin-1
  • Interleukin-6
  • Interleukin-8
  • N-acetylsphingosine
  • Sialoglycoproteins
  • N-caproylsphingosine
  • Macrophage Colony-Stimulating Factor
  • Sphingosine