Placenta-derived SOD3 deletion impairs maternal behavior via alterations in FGF/FGFR-prolactin signaling axis

Cell Rep. 2024 Oct 22;43(10):114789. doi: 10.1016/j.celrep.2024.114789. Epub 2024 Sep 25.

Abstract

Offspring growth requires establishing maternal behavior associated with the maternal endocrine profile. Placentae support the adaptations of the mother, producing bioactive molecules that affect maternal organs. We recently reported that placentae produce superoxide dismutase 3 (SOD3) that exerts sustained effects on the offspring liver via epigenetic modifications. Here, we demonstrate that placenta-specific Sod3 knockout (Sod3-/-) dams exhibited impaired maternal behavior and decreased prolactin levels. Most fibroblast growth factor (FGF)-regulated pathways were downregulated in the pituitary tissues from Sod3-/- dams. FGF1-, FGF2-, and FGF4-induced prolactin expression and signaling via the phosphoinositide 3-kinase (PI3K)-phospholipase C-γ1 (PLCγ1)-protein kinase-Cδ (PKC)δ axis were reduced in primary pituitary cells from Sod3-/- dams. Mechanistically, FGF1/FGF receptor (FGFR)2 expressions were inhibited by the suppression of the ten-eleven translocation (TET)/isocitrate dehydrogenase (IDH)/α-ketoglutarate pathway and DNA demethylation levels at the zinc finger and BTB domain containing 18 (ZBTB18)-targeted promoters of Fgf1/Fgfr2. Importantly, offspring from Sod3-/- dams also showed impaired nurturing behavior to their grandoffspring. Collectively, placenta-derived SOD3 promotes maternal behavior via epigenetic programming of the FGF/FGFR-prolactin axis.

Keywords: CP: Cell biology; CP: Developmental biology; DNA demethylation; exercise; grandoffspring; maternal exercise; nurturing; pituitary gland; placenta; placentokine; pregnancy.

MeSH terms

  • Animals
  • Female
  • Fibroblast Growth Factors* / genetics
  • Fibroblast Growth Factors* / metabolism
  • Gene Deletion
  • Maternal Behavior
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Pituitary Gland / metabolism
  • Placenta* / metabolism
  • Pregnancy
  • Prolactin* / metabolism
  • Receptor, Fibroblast Growth Factor, Type 2 / genetics
  • Receptor, Fibroblast Growth Factor, Type 2 / metabolism
  • Signal Transduction*
  • Superoxide Dismutase* / genetics
  • Superoxide Dismutase* / metabolism

Substances

  • Fibroblast Growth Factors
  • Superoxide Dismutase
  • Prolactin
  • Receptor, Fibroblast Growth Factor, Type 2