Estrogen-TGFbeta cross-talk in bone and other cell types: role of TIEG, Runx2, and other transcription factors

J Cell Biochem. 2008 Feb 1;103(2):383-92. doi: 10.1002/jcb.21425.

Abstract

It is well established that E(2) and TGFbeta have major biological effects in multiple tissues, including bone. The signaling pathways through which these two factors elicit their effects are well documented. However, the interaction between these two pathways and the potential consequences of cross-talk between E(2) and TGFbeta continue to be elucidated. In this prospectus, we present known and potential roles of TIEG, Runx2, and other transcription factors as important mediators of signaling between these two pathways.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Bone Remodeling / physiology
  • Bone and Bones / metabolism*
  • Core Binding Factor Alpha 1 Subunit / physiology*
  • DNA-Binding Proteins / physiology*
  • Dimerization
  • Early Growth Response Transcription Factors / physiology*
  • Estrogens / physiology*
  • Female
  • Kruppel-Like Transcription Factors / physiology*
  • MAP Kinase Signaling System / physiology
  • Male
  • Mice
  • Mice, Knockout
  • Osteoblasts / metabolism
  • Osteoclasts / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / physiology
  • Rats
  • Signal Transduction / physiology*
  • Transcription Factors / physiology*
  • Transcription, Genetic
  • Transforming Growth Factor beta / deficiency
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / physiology*

Substances

  • Core Binding Factor Alpha 1 Subunit
  • DNA-Binding Proteins
  • Early Growth Response Transcription Factors
  • Estrogens
  • KLF10 protein, human
  • Kruppel-Like Transcription Factors
  • Protein Isoforms
  • Tieg1 protein, mouse
  • Transcription Factors
  • Transforming Growth Factor beta