DHA-promoted repair of human corneal epithelial cells in high-glucose environment

Abstract Aim The purpose of this study was to evaluate DHA’s effect and relative mechanisms in diabetic keratopathy (DK) treatment by vitro study. Methods and materials: Using high glucose to make DK cell model; measuring cell apoptosis by flow cytometry and Hoechst 33342 staining; evaluating cell m...

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Bibliographic Details
Authors: HUANG,Chenchen, CHENG,Hong, ZHANG,Jing, ZHANG,Dachuan
Format: article
Status:Published version
Publication Date:2022
Country:Brasil
Institution:Sociedade Brasileira de Ciência e Tecnologia de Alimentos (SBCTA)
Repository:Food Science and Technology (Campinas)
Language:English
OAI Identifier:oai:scielo:S0101-20612022000100841
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0101-20612022000100841
Access Level:Open access
Keyword:DK
DHA
PEDE
TKE-2
Description
Summary:Abstract Aim The purpose of this study was to evaluate DHA’s effect and relative mechanisms in diabetic keratopathy (DK) treatment by vitro study. Methods and materials: Using high glucose to make DK cell model; measuring cell apoptosis by flow cytometry and Hoechst 33342 staining; evaluating cell migration abilities by wound healing assay; relative gene and proteins including PEDF, VEGF, Caspase-3, Caspase-9 and NF-κB(p65) expression by RT-qPCR and WB assay; And evaluatign PDEF and p-NF-κB(p65) protein expression by immunofluorescence detection. Results: After high glucose treatment, TKE-2 cell apoptosis was significantly increased and cell migration ability was significantly depressed with PEDF, Caspase-3, Caspase-9 and NF-κB(p65) gene and protein significantly increasing and VEGF expression significantly depressing (P < 0.001, respectively); with DHA supplement, TKE-2 cell biological activities were significantly improved with relative gene and proteins significantly changed; However, with DHA and PEDF supplement, DHA’s treatment was disappeared with PEDF, Caspase-3, Caspase-9 and NF-κB(p65) gene and protein significantly increasing and VEGF expression significantly depressing (P < 0.001, respectively). Conclusion: DHA had effects to improved DK by regulation PEDF pathway in vitro study.