TGFβ inducible early gene-1 knockout mice display defects in bone strength and microarchitecture

Sabine F. Bensamoun, John R. Hawse, Malayannan Subramaniam, Brice Ilharreborde, Armelle Bassillais, Claude L. Benhamou, Daniel G. Fraser, Merry J. Oursler, Peter C. Amadio, Kai Nan An, Thomas C. Spelsberg

Research output: Contribution to journalArticlepeer-review

53 Scopus citations


TGFβ inducible early gene-1 (TIEG) is a member of the Sp/Krüppel-like transcription factor family originally cloned from human osteoblasts. We have previously demonstrated that TIEG plays a role in the expression of important osteoblast marker genes and in the maturation/differentiation of osteoblasts. To elucidate the function of TIEG in skeletal development and maintenance, we have generated a TIEG knockout (KO) mouse. Three-point bending tests demonstrated that the femurs of TIEG KO mice are significantly weaker than those of wild-type animals. pQCT analysis of tibias revealed significant decreases in bone content, density and size in KO animals compared to wild-type mice. Micro-CT analysis of the femoral head and vertebrae revealed increases in femoral head trabecular separation and decreases in cortical bone thickness and vertebral bone volume in KO mice relative to wild-type controls. In addition, electron microscopy indicated a significant decrease in osteocyte number in the femurs of KO mice. Taken together, these data demonstrate that the bones of TIEG KO mice display an osteopenic phenotype with significantly weaker bones and reduced amounts of cortical and trabecular bone. In summary, an important role for TIEG in skeletal development and/or homeostasis is indicated.

Original languageEnglish (US)
Pages (from-to)1244-1251
Number of pages8
Issue number6
StatePublished - Dec 2006


  • Bone
  • Osteoblast
  • Osteopenia
  • TGFβ
  • TIEG

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Histology


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