Nmp4/CIZ contributes to fluid shear stress induced MMP-13 gene induction in osteoblasts

J Cell Biochem. 2007 Dec 1;102(5):1202-13. doi: 10.1002/jcb.21349.

Abstract

The expression of matrix metalloproteinase-13 (MMP-13), involved in bone turnover, is elevated in stretched MC3T3-E1 osteoblast-like cells. Strain-mediated forces impact bone remodeling due in large part to the movement of fluid through the canalicular-lacunar network. The resulting fluid shear stress (FSS) over the surface membranes of bone cells initiates bone remodeling. Although the nuclear events mediating putative FSS-induced changes in osteoblast MMP-13 transcription are unknown, previous studies with bone cells suggest an overlap between osteoblast FSS- and PTH-induced signal response pathways. MMP-13 PTH response is regulated by a 110 bp 5' regulatory region, conserved across the mouse, rat, and human genes, that supports the binding of numerous transcription factors including Runx2, c-fos/c-jun, Ets-1, and nuclear matrix protein 4/cas interacting zinc finger protein (Nmp4/CIZ) a nucleocytoplasmic shuttling trans-acting protein that attenuates PTH-driven transcription. Nmp4/CIZ also binds p130(cas), an adaptor protein implicated in mechanotransduction. Here we sought to determine whether Nmp4/CIZ contributes to FSS-induced changes in MMP-13 transcription. FSS (12 dynes/cm(2), 3-5 h) increased MMP-13 promoter-reporter activity approximately two-fold in MC3T3-E1 osteoblast-like cells attended by a comparable increase in mRNA expression. This was accompanied by a decrease in Nmp4/CIZ binding to its cis-element within the PTH response region, the mutation of which abrogated the MMP-13 response to FSS. Interestingly, FSS enhanced Nmp4/CIZ promoter activity and induced p130(cas) nuclear translocation. We conclude that the PTH regulatory region of MMP-13 also contributes to FSS response and that Nmp4/CIZ plays similar but distinct roles in mediating hormone- and FSS-driven induction of MMP-13 in bone cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3T3 Cells
  • Animals
  • Cell Culture Techniques
  • Cells, Cultured
  • Crk-Associated Substrate Protein / metabolism
  • Electrophoretic Mobility Shift Assay
  • Genes, Reporter
  • Luciferases / metabolism
  • Matrix Metalloproteinase 13 / biosynthesis*
  • Matrix Metalloproteinase 13 / genetics
  • Mechanotransduction, Cellular
  • Mice
  • Nuclear Matrix-Associated Proteins / genetics
  • Nuclear Matrix-Associated Proteins / metabolism*
  • Osteoblasts / cytology
  • Osteoblasts / metabolism*
  • Promoter Regions, Genetic
  • Protein Binding
  • RNA, Messenger / metabolism
  • Stress, Mechanical
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • Crk-Associated Substrate Protein
  • Nuclear Matrix-Associated Proteins
  • RNA, Messenger
  • Transcription Factors
  • Zfp384 protein, mouse
  • Luciferases
  • Matrix Metalloproteinase 13
  • Mmp13 protein, mouse