Acid sphingomyelinase involvement in tumor necrosis factor α-regulated vascular and steroid disruption during luteolysis in vivo

Luiz E. Henkes, Brian T. Sullivan, Maureen P. Lynch, Richard Kolesnick, Danielle Arsenault, Mark Puder, John S. Davis, Bo R. Rueda

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

TNF is well known for its role in inflammation, including direct effects on the vasculature. TNF also is implicated in the regulation of reproduction by its actions to affect ovarian steroidogenic cells and to induce apoptosis of corpus luteum (CL)-derived endothelial cells in vitro. We hypothesized that the disruption of TNF signaling would postpone the regression of the highly vascularized CL in vivo, and this effect could be replicated in mutant mouse models lacking TNF receptor (TNFRI-/-) and/or a critical enzyme of TNF signaling, acid sphingomyelinase (ASMase-/-). In the current study, the treatment of pseudopregnant mice with the luteolytic mediator prostaglandin F2-α (PGF) significantly increased TNF in the ovaries when compared with saline-treated controls. Treatment with PGF also reduced serum progesterone (P4) concentrations and caused involution of the CL. However, pretreatment of pseudopregnant mice with Etanercept (ETA), a TNF-neutralizing antibody, inhibited the PGF-induced decrease in P4 and delayed luteal regression. A similar outcome was evident in pseudopregnant TNFRI-/- animals. Treatment of luteal microvascular endothelial cells (MVECs) with TNF provoked a significant increase in ASMase activity when compared with the corresponding controls. Furthermore, TNF-induced MVEC death was inhibited in the ASMase-/- mice. The ASMase-/- mice displayed no obvious evidence of luteal regression 24 h after treatment with PGF and were resistant to the PGF-induced decrease in P4. Together these data provide evidence that TNF plays an active role in luteolysis. Further studies are required to determine the deleterious effects of antiinflammatory agents on basic ovarian processes.

Original languageEnglish (US)
Pages (from-to)7670-7675
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume105
Issue number22
DOIs
StatePublished - Jun 3 2008

Keywords

  • Corpus luteum
  • Cytokines
  • Endothelial cells
  • Ovary
  • Progesterone

ASJC Scopus subject areas

  • General

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