Vitamin C Inhibit The Proliferation, Migration And Epithelial-Mesenchymal-Transition Of Lens Epithelial Cells By Destabilizing Hif-1 Alpha

Posterior capsular opacification (PCO), the main complication of cataract surgery, is mainly caused by the proliferation, migration, and epithelial-mesenchymal transition (EMT) of the residual lens epithelial cells (LECs). Vitamin C was reported to reduce the risk of forming a cataract. However, there has been no study showing the association between vitamin C and PCO. In this study, we found that vitamin C could inhibit the migration and proliferation of human lens epithelial cells. We also found that vitamin C could increase the proline hydroxylation of HIF-1 alpha and reduce the activity of HIF-1 alpha. Moreover, vitamin C could not inhibit the activity of proline-mutant HIF-1 alpha (402/564). Overexpression of wild-type HIF-1 alpha or proline-mutant HIF-1 alpha was found to increase the proliferation and migration of human lens epithelial cells. Differently, vitamin C could inhibit the proliferation and migration in wildtype HIF-1 alpha-overexpressing lens epithelial cells but not the proline-mutant HIF-1 alpha-overexpressing cells. Additionally, vitamin C was also found to inhibit the expression of EMT transcription factors TWIST. We then found that vitamin C could repress the EMT phenotypes induced by the overexpression of wild-type HIF-1 alpha but not the proline-mutant HIF-1 alpha. These results provide evidence that vitamin C plays a role in the repression of proliferation, migration, and EMT of human lens epithelial cells by destabilizing HIF-1 alpha.