Antagonists of retinoic acid and BMP4 affect fetal mouse osteogenesis and odontoblast differentiation

Despina S Koussoulakou1, Lukas H Margaritis, Stauros L Koussoulakos

  • 1Department of Cell Biology and Biophysics, Faculty of Biology, N. & K. University of Athens, Panepistimiopolis 15784, Greece.

Insights

Citral and anti-BMP4 antibody treatments in pregnant mice showed minor, temporary effects on fetal cranial bone development and tooth formation, concluding both substances are safe at tested doses.

Area of Science:

  • Developmental biology
  • Osteogenesis research
  • Toxicology studies

Background:

  • Retinoic acid and bone morphogenetic protein (BMP4) are vital for vertebrate development.
  • Potential human exposure to retinoic acid inhibitors and BMP4 neutralizers necessitates safety assessments.

Purpose of the Study:

  • To evaluate the impact of citral (retinoic acid synthesis inhibitor) and anti-BMP4 antibody on fetal cranial osteogenesis and odontoblast differentiation.
  • To determine the safety of these compounds for potential clinical use by assessing side effects.

Main Methods:

  • Pregnant mice were injected with citral or anti-BMP4 antibody on day 9 of gestation.
  • Newborns were analyzed macroscopically, stereoscopically (histochemistry), and microscopically (histology, immunohistochemistry for apoptosis).

Main Results:

  • Citral administration mimicked hypovitaminosis A, causing cranial chondrogenesis and osteogenesis retardation; no apoptosis was observed in teeth.
  • Anti-BMP4 antibody caused transient interference with odontoblast differentiation and pre-dentin production, with delayed ossification in alveoli.
  • Adult offspring exhibited largely normal phenotypes, indicating resilience to the treatments.

Conclusions:

  • Citral and anti-BMP4 antibody, at the tested concentrations, demonstrate a low risk profile for fetal development.
  • These findings support the safety of citral and anti-BMP4 antibody, paving the way for future clinical considerations.

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