Nicotine inhibits palatal fusion and modulates nicotinic receptors and the PI-3 kinase pathway in medial edge epithelia

Orthod Craniofac Res. 2003 Aug;6(3):129-42. doi: 10.1034/j.1600-0544.2003.02236.x.

Abstract

Objectives: To analyze the effects of nicotine on palatal fusion inhibition in vitro and determine if nicotine modulated transforming growth factor beta3 or phosphatidylinositol-3 kinase signaling. A second objective was to determine the localization and regulation of nicotinic receptors in the medial edge epithelia (MEE) during palatal fusion.

Design: Palatal shelves from embryonic day (E) 13.5 mice were cultured in serum free media and treated with 0, 0.06, 0.6, or 6 mM nicotine, nicotinic receptor antagonist alpha-bungarotoxin, or the combination of nicotine and alpha-bungarotoxin. Tissues harvested at 72 h were analyzed for epithelial-mesenchymal transformation (EMT) and fusion. MEE samples collected at 20 h were analyzed for phosphorylated Akt-Ser473, phosphorylated Smad2, and nicotinic receptors.

Results: Nicotine inhibited palatal fusion in vitro in a dose dependent manner. Activated Akt-Ser473 was greater in control MEE than in nicotine treated tissues; while there was no difference in activated Smad2 between groups. The alpha7 subunit of nicotinic receptor was expressed in MEE during palate fusion and increased in nicotine treated tissues. Alpha-bungarotoxin did not rescue the nicotine treated palates.

Conclusion: Nicotine treatment had no effect on Smad2, but caused a down regulation of the PI-3 kinase pathway that may have contributed to inhibiting palatal fusion in vitro.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bungarotoxins / pharmacology
  • Cleft Palate / chemically induced*
  • Cleft Palate / embryology*
  • DNA-Binding Proteins / metabolism
  • Epithelium / drug effects
  • Epithelium / embryology
  • Immunohistochemistry
  • Mesoderm / drug effects
  • Mice
  • Mice, Inbred Strains
  • Microscopy, Confocal
  • Nicotine / toxicity*
  • Nicotinic Agonists / toxicity*
  • Organ Culture Techniques
  • Palate, Hard / drug effects*
  • Palate, Hard / embryology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Receptors, Nicotinic / metabolism
  • Signal Transduction / drug effects*
  • Smad2 Protein
  • Trans-Activators / metabolism
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta3

Substances

  • Bungarotoxins
  • DNA-Binding Proteins
  • Nicotinic Agonists
  • Phosphoinositide-3 Kinase Inhibitors
  • Proto-Oncogene Proteins
  • Receptors, Nicotinic
  • Smad2 Protein
  • Smad2 protein, mouse
  • Tgfb3 protein, mouse
  • Trans-Activators
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta3
  • Nicotine
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt