Loss of osteopontin perturbs the epithelial-mesenchymal transition in an injured mouse lens epithelium

Lab Invest. 2007 Feb;87(2):130-8. doi: 10.1038/labinvest.3700508. Epub 2007 Jan 8.

Abstract

We previously reported that osteopontin (OPN), a matrix structural glycophosphoprotein, is upregulated in the injured mouse lens prior to the epithelial-mesenchymal transition (EMT). Here, we investigated the role of this protein in EMT of the lens epithelium during wound healing. The crystalline lens was injured by needle puncture in OPN-null (KO, n=40) and wild-type (WT, n=40) mice. The animals were killed at day 1, 2, 5, and 10 postinjury. Immunohistochemistry was employed to detect alpha-smooth muscle action (alphaSMA), a marker of EMT, collagen type I, transforming growth factor beta1 (TGFbeta1), TGFbeta2, and phospho-Smad2/3. Cell proliferation was assayed by examining uptake of bromodeoxyuridine (BrdU). The results showed that injury-induced EMT of mouse lens epithelium, as evaluated by histology, expression pattern of alphaSMA and collagen I, was altered in the absence of OPN with reduced phospho-Smad2/3 signaling. Upregulation of TGFbeta1 and TGFbeta2 in the epithelium was also inhibited. Cell proliferation was more active in KO mice as compared with WT mice at day 1 and 2, but not at day 5 and 10. An in vitro experiment shows OPN facilitates cell adhesion of lens epithelial cell line. OPN is required for activation of Smad2/3 signal in an injured lens epithelium and lens cell EMT.

Publication types

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

MeSH terms

  • Actins / metabolism
  • Animals
  • Bromodeoxyuridine
  • Cell Adhesion / physiology
  • Collagen Type I / metabolism
  • Epithelial Cells / metabolism*
  • Immunohistochemistry
  • Lens, Crystalline / cytology*
  • Lens, Crystalline / injuries*
  • Lens, Crystalline / metabolism
  • Mesoderm / cytology*
  • Mice
  • Mice, Knockout
  • Osteopontin / deficiency
  • Osteopontin / genetics
  • Osteopontin / metabolism*
  • Smad2 Protein / metabolism
  • Transforming Growth Factor beta1 / metabolism
  • Wound Healing / physiology*

Substances

  • Actins
  • Collagen Type I
  • Smad2 Protein
  • Smad2 protein, mouse
  • Transforming Growth Factor beta1
  • Osteopontin
  • Bromodeoxyuridine