Requirement for TGFbeta receptor signaling during terminal lens fiber differentiation

Development. 2001 Oct;128(20):3995-4010. doi: 10.1242/dev.128.20.3995.


Several families of growth factors have been identified as regulators of cell fate in the developing lens. Members of the fibroblast growth factor family are potent inducers of lens fiber differentiation. Members of the transforming growth factor beta (TGFbeta) family, particularly bone morphogenetic proteins, have also been implicated in various stages of lens and ocular development, including lens induction and lens placode formation. However, at later stages of lens development, TGFbeta family members have been shown to induce pathological changes in lens epithelial cells similar to those seen in forms of human subcapsular cataract. Previous studies have shown that type I and type II TGFbeta receptors, in addition to being expressed in the epithelium, are also expressed in patterns consistent with a role in lens fiber differentiation. In this study we have investigated the consequences of disrupting TGFbeta signaling during lens fiber differentiation by using the mouse alphaA-crystallin promoter to overexpress mutant (kinase deficient), dominant-negative forms of either type I or type II TGFbeta receptors in the lens fibers of transgenic mice. Mice expressing these transgenes had pronounced bilateral nuclear cataracts. The phenotype was characterized by attenuated lens fiber elongation in the cortex and disruption of fiber differentiation, culminating in fiber cell apoptosis and degeneration in the lens nucleus. Inhibition of TGFbeta signaling resulted in altered expression patterns of the fiber-specific proteins, alpha-crystallin, filensin, phakinin and MIP. In addition, in an in vitro assay of cell migration, explanted lens cells from transgenic mice showed impaired migration on laminin and a lack of actin filament assembly, compared with cells from wild-type mice. These results indicate that TGFbeta signaling is a key event during fiber differentiation and is required for completion of terminal differentiation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / metabolism
  • Activin Receptors, Type I / genetics
  • Activin Receptors, Type I / physiology*
  • Animals
  • Apoptosis
  • Aquaporins
  • Cataract / embryology
  • Cataract / genetics
  • Cataract / metabolism
  • Cell Differentiation
  • Cell Division
  • Cell Movement
  • Crystallins / genetics
  • Eye Proteins / genetics
  • Gene Expression Regulation, Developmental
  • Humans
  • In Situ Hybridization
  • Intermediate Filament Proteins / genetics
  • Lens, Crystalline / cytology
  • Lens, Crystalline / embryology*
  • Lens, Crystalline / metabolism
  • Membrane Glycoproteins*
  • Mice
  • Mice, Transgenic
  • Protein Serine-Threonine Kinases
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II
  • Receptors, Transforming Growth Factor beta / genetics
  • Receptors, Transforming Growth Factor beta / physiology*
  • Signal Transduction


  • Actins
  • Aquaporins
  • Crystallins
  • Eye Proteins
  • Intermediate Filament Proteins
  • Membrane Glycoproteins
  • Receptors, Transforming Growth Factor beta
  • aquaporin 0
  • filensin
  • phakinin
  • Protein Serine-Threonine Kinases
  • Activin Receptors, Type I
  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II