The endocytic recycling regulatory protein EHD1 Is required for ocular lens development

Dev Biol. 2015 Dec 1;408(1):41-55. doi: 10.1016/j.ydbio.2015.10.005. Epub 2015 Oct 9.

Abstract

The C-terminal Eps15 homology domain-containing (EHD) proteins play a key role in endocytic recycling, a fundamental cellular process that ensures the return of endocytosed membrane components and receptors back to the cell surface. To define the in vivo biological functions of EHD1, we have generated Ehd1 knockout mice and previously reported a requirement of EHD1 for spermatogenesis. Here, we show that approximately 56% of the Ehd1-null mice displayed gross ocular abnormalities, including anophthalmia, aphakia, microphthalmia and congenital cataracts. Histological characterization of ocular abnormalities showed pleiotropic defects that include a smaller or absent lens, persistence of lens stalk and hyaloid vasculature, and deformed optic cups. To test whether these profound ocular defects resulted from the loss of EHD1 in the lens or in non-lenticular tissues, we deleted the Ehd1 gene selectively in the presumptive lens ectoderm using Le-Cre. Conditional Ehd1 deletion in the lens resulted in developmental defects that included thin epithelial layers, small lenses and absence of corneal endothelium. Ehd1 deletion in the lens also resulted in reduced lens epithelial proliferation, survival and expression of junctional proteins E-cadherin and ZO-1. Finally, Le-Cre-mediated deletion of Ehd1 in the lens led to defects in corneal endothelial differentiation. Taken together, these data reveal a unique role for EHD1 in early lens development and suggest a previously unknown link between the endocytic recycling pathway and regulation of key developmental processes including proliferation, differentiation and morphogenesis.

Keywords: Apoptosis; Corneal endothelium; EHD1; Endocytic recycling; Lens development; Lens epithelium; Polarity; Proliferation.

Publication types

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

MeSH terms

  • Animals
  • Cataract / complications
  • Cataract / embryology
  • Cataract / genetics
  • Cataract / pathology
  • Cell Differentiation
  • Cell Polarity
  • Cell Survival
  • Embryo, Mammalian / pathology
  • Endocytosis*
  • Endothelium, Corneal / metabolism
  • Endothelium, Corneal / pathology
  • Epithelial Cells / pathology
  • Eye Abnormalities / genetics
  • Eye Abnormalities / pathology
  • Gene Deletion
  • Gene Expression Regulation, Developmental
  • Lens, Crystalline / embryology*
  • Lens, Crystalline / metabolism*
  • Lens, Crystalline / pathology
  • Mice, Knockout
  • Microphthalmos / complications
  • Microphthalmos / embryology
  • Microphthalmos / genetics
  • Phenotype
  • Vesicular Transport Proteins / deficiency
  • Vesicular Transport Proteins / metabolism*

Substances

  • Ehd1 protein, mouse
  • Vesicular Transport Proteins