Disruption of Rest Leads to the Early Onset of Cataracts with the Aberrant Terminal Differentiation of Lens Fiber Cells

PLoS One. 2016 Sep 15;11(9):e0163042. doi: 10.1371/journal.pone.0163042. eCollection 2016.

Abstract

REST (RE1-silencing transcription factor, also called Nrsf) is involved in the maintenance of the undifferentiated state of neuronal stem/progenitor cells in vitro by preventing precocious expression of neuronal genes. REST expression was then decreased in developing neurons to down-regulate neuronal genes which allow their maturation. However, the function of REST during neurogenesis in vivo remains to be elucidated because of the early embryonic lethal phenotype of conventional Rest knockout mice. In order to investigate the role of REST in ocular tissues, we generated and examined the mice evoking genetic ablation to Rest specifically to neural tissues including ocular tissue. We used a Sox1-Cre allele to excise the floxed Rest gene in the early neural tissues including the lens and retinal primordia. The resulting Rest conditional knockout (CKO) and co cntrol mice were used in comparative morphological, histological, and gene expression analyses. Rest CKO mice had an abnormal lens morphology after birth. The proliferation of lens epithelial cells was likely to be slightly reduced, and vacuoles formed without a visible increase in apoptotic cells. Although the aberrant expression of late onset cataract marker proteins was not detected, the expression of Notch signaling-related genes including a previously identified REST-target gene was up-regulated around birth, and this was followed by the down-regulated expression of lens fiber regulators such as c-Maf and Prox1. Rest CKO induces a unique cataract phenotype just after birth. Augmented Notch signaling and the down-regulated expression of lens fiber regulator genes may be responsible for this phenotype. Our results highlight the significance of REST function in lens fiber formation, which is necessary for maintaining an intact lens structure.

MeSH terms

  • Animals
  • Cataract / pathology*
  • Cell Differentiation*
  • Cell Proliferation
  • Gene Expression Profiling
  • Lens, Crystalline / cytology*
  • Mice
  • Mice, Transgenic
  • Repressor Proteins / genetics*

Substances

  • RE1-silencing transcription factor
  • Repressor Proteins

Grants and funding

This research was funded by a grant from the Japan Science and Technology Agency and by Grants-in-Aid for Scientific Research by the JSPS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.