Abstract

Bone morphogenetic proteins (BMPs), a member of the transforming growth factor β (TGF-β) superfamily, are abundant in human ocular tissues and play an important role in lens development. Targeted deletion of BMP-4 in mice results in failure of lens placode formation. Following lens maturation, the formation of senile cataracts is demonstrably associated with free radical-related oxidative stress. Previous studies reported that BMPs play an antiapoptotic role in cells under oxidative stress, and the BMP-4 signal is important in inflammation regulation and homeostasis. BMP-4 evidently suppressed the apoptosis of human lens epithelial cells (HLECS) under oxidative stress induced by H2O2. This protective antiapoptotic effect is partly due to a decrease in caspase-3 activity and reactive oxygen species (ROS) level. Furthermore, the expression of activating transcription factor- (ATF-) 6 and Krüppel-like factor- (KLF-) 6 increased under oxidative stress and decreased after BMP-4 treatment.

Highlights

  • Cataracts are a widely prevalent eye disease, which are the leading cause of blindness worldwide and involve a complicated pathogenesis

  • The cultured cells were stimulated with H2O2 for 1.5 h, 100 ng/mL Bone morphogenetic proteins (BMPs)-4 in serum-free medium was added for 24 h

  • The results demonstrated that H2O2 markedly enhanced the production of reactive oxygen species (ROS); when BMP-4 was added, there was a significant reduction in the level of ROS (Figures 6(a) and 6(b))

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Summary

Introduction

Cataracts are a widely prevalent eye disease, which are the leading cause of blindness worldwide and involve a complicated pathogenesis. The bone morphogenetic protein (BMP) is a multifunctional growth factor belonging to the transforming growth factor β (TGF-β) superfamily that has been shown to play important roles in both the development and regeneration of different tissues [3]. Previous research has shown that BMPs and their receptors play an important role in the development of lens during eyeball development [4]. BMPs are highly expressed in mouse embryos, and blocking of BMP signals in the lens ectoderm of cultured mouse embryos prevented lens formation. Previous studies have reported that BMPs play an antiapoptotic role in some cells under oxidative stress, and the BMP-4 signal is important in the regulation of inflammation and homeostasis [8, 9]. Limited information is available regarding the role and mechanism of BMP-4 in human lens

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