Nicotine induces cell proliferation in association with cyclin D1 up-regulation and inhibits cell differentiation in association with p53 regulation in a murine pre-osteoblastic cell line

Biochem Biophys Res Commun. 2008 Dec 5;377(1):126-30. doi: 10.1016/j.bbrc.2008.09.114. Epub 2008 Oct 1.

Abstract

Recent studies have suggested that nicotine critically affects bone metabolism. Many studies have examined the effects of nicotine on proliferation and differentiation, but the underlying molecular mechanisms remain unclear. We examined cell cycle regulators involved in the proliferation and differentiation of MC3T3-E1 cells. Nicotine induced cell proliferation in association with p53 down-regulation and cyclin D1 up-regulation. In differentiated cells, nicotine reduced alkaline phosphatase activity and mineralized nodule formation in dose-dependent manners. Furthermore, p53 expression was sustained in nicotine-treated cells during differentiation. These findings indicate that nicotine promotes the cell cycle and inhibits differentiation in association with p53 regulation in pre-osteoblastic cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcification, Physiologic / drug effects
  • Cell Cycle / drug effects
  • Cell Differentiation / drug effects*
  • Cell Line
  • Cell Proliferation / drug effects*
  • Cyclin D1 / metabolism*
  • Mice
  • Nicotine / pharmacology*
  • Osteoblasts / cytology
  • Osteoblasts / drug effects*
  • Osteoblasts / metabolism
  • Receptors, Nicotinic / drug effects
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation

Substances

  • Receptors, Nicotinic
  • Tumor Suppressor Protein p53
  • Cyclin D1
  • Nicotine