Up-regulation of NDRG2 in senescent lens epithelial cells contributes to age-related cataract in human

PLoS One. 2011;6(10):e26102. doi: 10.1371/journal.pone.0026102. Epub 2011 Oct 17.

Abstract

Background: Human N-Myc downstream regulated gene2 (NDRG2), a novel gene has been cloned and shown to be related to a number of cellular processes, including proliferation, differentiation, stress, and apoptosis. NDRG2 has also been linked to age-related Alzheimer's disease. Since the role of this gene in senescence is limited, we have investigated the potential role of NDRG2 in human lens epithelial cells (HLECs), a paradigm implicated in age-related cataract.

Methodology/principal findings: Cultured HLECs (SRA01/04) were subjected to prolonged exposure to low dose of H(2)O(2) to simulate senescence. After being exposed to 50 µM H(2)O(2) for 2 weeks, HLECs senescent-morphological changes appeared, cell viability decreased dramatically, cell proliferation reduced from 37.4% to 16.1%, and senescence-associated β-galactosidase activity increased from 0 to 90.3%. Ndrg2 protein expression was also significantly increased in these senescent cells. To induce overexpression of NDRG2, SRA01/04 cells were infected with the adenoviral vector of NDRG2. In these cells, overexpression of NDRG2 resulted in a fibroblast-like appearance and the cell viability decreased about 20%. In addition, the NDRG2-overexpression cells demonstrated 20% lower viability when exposed to 50-200 µM H(2)O(2) for acute oxidative stress. Furthermore, the expression of NDRG2 from age-related cataracts was up-regulated 2-fold at both mRNA and protein levels compared with the clear lenses.

Conclusions/significance: NDRG2 is up regulated not only in the ageing process of HLECs in vitro but also in the cells from human age-related cortical cataract in vivo. Up-regulation of NDRG2 induces cell morphological changes, reduces cell viability, and especially lowers cellular resistance to oxidative stress. NDRG2-mediated affects in HLECs may associate with age-related cataract formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cataract / etiology*
  • Cell Proliferation
  • Cell Shape
  • Cell Survival
  • Cells, Cultured
  • Cellular Senescence / drug effects*
  • Epithelial Cells / metabolism*
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Lens, Crystalline / cytology*
  • Oxidative Stress
  • Tumor Suppressor Proteins / analysis
  • Tumor Suppressor Proteins / physiology*
  • Up-Regulation

Substances

  • NDRG2 protein, human
  • Tumor Suppressor Proteins
  • Hydrogen Peroxide