Sfrp1 and Sfrp2 are not involved in Wnt/β-catenin signal silencing during lens induction but are required for maintenance of Wnt/β-catenin signaling in lens epithelial cells

• Published in: Developmental biology 2013-12, Vol.384 (2), p.181-193
• Main Authors: Sugiyama, Yuki, Shelley, Elizabeth J., Wen, Li, Stump, Richard J.W., Shimono, Akihiko, Lovicu, Frank J., McAvoy, John W.
• Format: Article
• Language: English
• Subjects: Animals; antagonists; Base Sequence; beta Catenin - metabolism; Cell Proliferation; DNA Primers; epithelial cells; Epithelial Cells - cytology; epithelium; eye lens; Intercellular Signaling Peptides and Proteins - genetics; Intercellular Signaling Peptides and Proteins - physiology; Lens development; Lens epithelial cells; Lens, Crystalline - cytology; Lens, Crystalline - metabolism; Membrane Proteins - genetics; Membrane Proteins - physiology; Mice; Mice, Knockout; Polymerase Chain Reaction; Secreted frizzled-related protein; Signal Transduction; TCF/Lef activity; Wnt Proteins - metabolism; Wnt/β-catenin
• ISSN: 0012-1606; 1095-564X
• DOI: 10.1016/j.ydbio.2013.10.008

During eye lens development, regulation of Wnt/β-catenin signaling is critical for two major processes: initially it must be silent in the lens placode for lens development to proceed, but subsequently it is required for maintenance of the lens epithelium. It is not known how these different phases of Wnt/β-catenin activity/inactivity are regulated. Secreted frizzled related protein-2 (Sfrp2), a putative Wnt-Fz antagonist, is expressed in lens placode and in lens epithelial cells and has been put forward as a candidate for regional Wnt/β-catenin pathway regulation. Here we show its closely-related isoform, Sfrp1, has a complimentary pattern of expression in the lens, being absent from the placode and epithelium but expressed in the fibers. As mice with single knockouts of Sfrp1 or Sfrp2 had no defects in lens formation, we examined lenses of Sfrp1 and Sfrp2 double knockout (DKO) mice and showed that they formed lens placode and subsequent lens structures. Consistent with this we did not observe ectopic TCF/Lef activity in lens placode of DKOs. This indicates that Sfrp1 and Sfrp2 individually, or together, do not constitute the putative negative regulator that blocks Wnt/β-catenin signaling during lens induction. In contrast, Sfrp1 and Sfrp2 appear to have a positive regulatory function because Wnt/β-catenin signaling in lens epithelial cells was reduced in Sfrp1 and Sfrp2 DKO mice. Lenses that formed in DKO mice were smaller than controls and exhibited a deficient epithelium. Thus Sfrps play a role in lens development, at least in part, by regulating aspects of Wnt/β-catenin signaling in lens epithelial cells. •Sfrps play a role in lens development.•Sfrps function by regulating aspects of Wnt/β-catenin signaling.•Sfrp1/2 do not negatively regulate Wnt/β-catenin signaling in lens.•Sfrp1 and Sfrp2 have a positive regulatory function for Wnt/β-catenin signaling.