Blue light attenuates TGF-β2-induced epithelial-mesenchymal transition in human lens epithelial cells via autophagy impairment

• Published in: BMC ophthalmology Vol. 22; no. 1; pp. 1 - 456
• Main Authors: Zhang, Dongyan, Zhu, Hong, Yu, Xin, Wang, Liyin, Wen, Yingying, Zhang, Liyue, Tong, Jianping, Shen, Ye
• Format: Journal Article
• Language: English
• Published: London BioMed Central 28.11.2022; BMC
• Subjects: Antibodies; Autophagy; Blue light; Cancer; Cataracts; Cell activation; Cell growth; Cell migration; Chloroquine; Circadian rhythm; Epithelial cells; Epithelial-mesenchymal transition; Eye diseases; Fibroblasts; Gene expression; Human lens epithelial cells; Immunofluorescence; Light; Medical research; Membranes; Mesenchyme; Ophthalmology; Proteins; Rapamycin; Transmission electron microscopy; Western blotting; Wound healing
• ISSN: 1471-2415; 1471-2415
• DOI: 10.1186/s12886-022-02691-6

Abstract Background Pathogenesis of posterior capsular opacification (PCO) was related to pathological epithelial-mesenchymal transition (EMT) of lens epithelial cells (LECs). It has been reported that blue light could have an effect on EMT. This study aims to elucidate the role and potential mechanism of autophagy in EMT after blue light exposure in LECs. Methods HLE-B3 cells were treated with TGF-β2 with different concentration and time to induce EMT as a model of PCO in vitro. Cells were exposed to blue light with or without TGF-β2. The expression levels of EMT-associated markers were analyzed by qRT-PCR, western blotting and cell migration ability was determined by transwell migration assay and wound healing assay. The expressions of autophagy-related proteins were analyzed by western blotting, immunofluorescence and transmission electron microscopy. Rapamycin and chloroquine were utilized in cells for autophagy activation and inhibition. Results TGF-β2 induced autophagy activation during EMT progression in HLE-B3 cells in a dose- and time-dependent manner. Blue light exposure inhibited TGF-β2-induced EMT characterized by inhibited expression of EMT related markers and reduced migration capacity. Meanwhile, blue light exposure impaired autophagy activated by TGF-β2. Furthermore, Autophagy activation with rapamycin rescued EMT attenuated by blue light. Autophagy inhibition with chloroquine reduced TGF-β2-induced EMT in HLE-B3 cells. Conclusion Blue light exposure had inhibited effects on TGF-β2-induced EMT in LECs through autophagy impairment, which provides a new insight on prevention and treatment of PCO.