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Updated: Jun 19, 2026

4-Dimensional Imaging of Zebrafish Optic Cup Morphogenesis
07:26

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Published on: May 26, 2021

Essential role for Pbx1 in corneal morphogenesis.

Mark J Murphy1, Bozena K Polok, Daniel F Schorderet

  • 1Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.

Investigative Ophthalmology & Visual Science
|October 3, 2009
PubMed
Summary

The Pbx1 proto-oncogene is essential for corneal development. Its deletion in mice causes severe corneal dystrophy, highlighting its role in maintaining corneal structure and function.

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Area of Science:

  • Developmental Biology
  • Ophthalmology
  • Genetics

Background:

  • Pbx TALE homeodomain proteins interact with Hox proteins, crucial for cell fate.
  • Pbx1 is a key regulator in developmental processes.

Purpose of the Study:

  • To investigate the function of Pbx1 in the mouse corneal epithelium.
  • To understand the role of Pbx1 in corneal morphogenesis.

Main Methods:

  • Used Pbx1(f/f) mice crossed with K14-Cre mice for tissue-specific deletion.
  • Analyzed eyes via histologic and molecular methods.

Main Results:

  • Pbx1 deletion caused corneal dystrophy and clouding from birth, worsening with age.
  • Observed corneal epithelial thickening, stromal infiltration by atypical basal cells, and collagen disorganization.
  • Found high epithelial cell turnover, perturbed developmental regulators, and aberrant differentiation.

Conclusions:

  • Pbx1 is essential for normal corneal development and morphogenesis.
  • Pbx1 plays a critical role in maintaining corneal structure and barrier function.