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Reactive oxygen species mediates a metabolic memory of high glucose stress signaling in bovine retinal pericytes

Reactive oxygen species mediates a metabolic memory of high glucose stress signaling in bovine retinal pericytes
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摘要 AIM: To investigate the role of reactive oxygen species (ROS) and antioxidant mechanism underlying the metabolic memory of bovine retinal pericytes (BRPs) induced by high glucose.METHODS: Effects of high glucose levels and culture time on BRPs viability were evaluated by CCK-8. BRPs were grown in high-glucose media (30 mmol/L) for 4d followed by culture in normal glucose condition (5.6 mmol/L) for 4d in an experimental group. In contrast, in negative and positive control groups, BRPs were grown in either normal-glucose media or high-glucose media for 8d, respectively. The ROS levels, apoptosis, the expression and activity of manganese superoxide dismutase (MnSOD) in BRPs, as well as the protective effect of adeno-associated viral (AAV)-mediated over expression of MnSOD were determined separately by DCHFA, ELISA and Western blot.RESULTS: Comparing the result of cells apoptosis, activity and protein expression of MnSOD and caspase-3, the cell culture system that exposed in sequence in 30 mmol/L and normal glucose for 4d was demonstrated as a suitable model of metabolic memory. Furthermore, delivery of antioxidant gene MnSOD can decrease BRPs apoptosis, reduce activated caspase-3, and reverse hyperglycemic memory by reducing the ROS of mitochondria.CONCLUSION: Increased ROS levels and decreased MnSOD levels may play important roles in pericyte loss of diabetic retinopathy. BRPs cultured in high glucose for 4d followed by normal glucose for 4d could be an appropriate model of metabolic memory. rAAV-MnSOD gene therapy provides a promising strategy to inhibit this blinding disease. AIM: To investigate the role of reactive oxygen species(ROS) and antioxidant mechanism underlying the metabolic memory of bovine retinal pericytes(BRPs) induced by high glucose.METHODS: Effects of high glucose levels and culture time on BRPs viability were evaluated by CCK-8. BRPs were grown in high-glucose media(30 mmol/L) for 4 d followed by culture in normal glucose condition(5.6 mmol/L) for 4 d in an experimental group. In contrast, in negative and positive control groups, BRPs were grown in either normal-glucose media or high-glucose media for 8 d, respectively. The ROS levels, apoptosis, the expression and activity of manganese superoxide dismutase(MnSOD) in BRPs, as well as the protective effect of adeno-associated viral(AAV)-mediated over expression of MnSOD were determined separately by DCHFA, ELISA and Western blot.RESULTS: Comparing the result of cells apoptosis, activity and protein expression of MnSOD and caspase-3, the cell culture system that exposed in sequence in 30 mmol/L and normal glucose for 4 d was demonstrated as a suitable model of metabolic memory. Furthermore, delivery of antioxidant gene MnSOD can decrease BRPs apoptosis, reduce activated caspase-3, and reverse hyperglycemic memory by reducing the ROS of mitochondria. CONCLUSION: Increased ROS levels and decreased Mn SOD levels may play important roles in pericyte loss of diabetic retinopathy. BRPs cultured in high glucose for 4 d followed by normal glucose for 4 d could be an appropriate model of metabolic memory. rAAV-MnSOD gene therapyprovides a promising strategy to inhibit this blinding disease.
出处 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2019年第7期1067-1074,共8页 国际眼科杂志(英文版)
基金 Supported by the National Natural Science Foundation of China(No.81371054 No.81500746) Natural Science Foundation of Hunan Province(No.2014SK2010 No.2018JJ2576)
关键词 DIABETIC RETINOPATHY metabolic memory manganese superoxide DISMUTASE molecular THERAPEUTICS reactive oxygen species diabetic retinopathy metabolic memory manganese superoxide dismutase molecular therapeutics reactive oxygen species
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