机构地区:[1]Fujian Institute of Ophthalmology, the First Affiliated Hospital of Fujian Medical University
出 处:《International Journal of Ophthalmology(English edition)》2016年第1期15-20,共6页国际眼科杂志(英文版)
基 金:Supported by the National Natural Science Foundation of China(No.81070715);Innovative Platform Foundation of Fujian Province;China(No.2010Y2003)
摘 要:AIM:To investigate the role of Aquaporin-1(AQP-1)in lens epithelial cells(LECs)and its potential target genes.AQP-1 is specifically expressed in LECs of eyes and is significant for lens homeostasis and transparency maintenance.Herein,AQP-1 expression in LECs was investigated to evaluate its influence on cell survival in association with its potential role in cataract formation.·M ETHODS:LECs were transfected with lentivirus carrying AQP-1 small interfering RNA(si RNA).Real-time polymerase chain reaction(PCR)and Western blotting were conducted to detect AQP-1 expression in LECs from different groups.Meanwhile,cell counting kit-8(CCK-8)assay and flow cytometry were performed to measure LEC proliferation and apoptosis,respectively.·RESULTS:AQP-1 expression was significantly reduced in LECs,both at m RNA and protein levels(〈0.05),after si RNA treatment.Decreased cell viability was detected by CCK-8 assay in LECs with si RNA interference,compared to control cells(〈0.05).The apoptosis rate significantly increased in cells after si RNA interference(〈0.05).·CONCLUSION:The decreased cell viability following AQP-1 down regulation is largely due to its induction of apoptosis of LECs.AQP-1 reduction might lead to changes of physiological functions in LECs,which might be associated with the occurrence and development of cataracts.AIM:To investigate the role of Aquaporin-1(AQP-1)in lens epithelial cells(LECs)and its potential target genes.AQP-1 is specifically expressed in LECs of eyes and is significant for lens homeostasis and transparency maintenance.Herein,AQP-1 expression in LECs was investigated to evaluate its influence on cell survival in association with its potential role in cataract formation.·M ETHODS:LECs were transfected with lentivirus carrying AQP-1 small interfering RNA(si RNA).Real-time polymerase chain reaction(PCR)and Western blotting were conducted to detect AQP-1 expression in LECs from different groups.Meanwhile,cell counting kit-8(CCK-8)assay and flow cytometry were performed to measure LEC proliferation and apoptosis,respectively.·RESULTS:AQP-1 expression was significantly reduced in LECs,both at m RNA and protein levels(〈0.05),after si RNA treatment.Decreased cell viability was detected by CCK-8 assay in LECs with si RNA interference,compared to control cells(〈0.05).The apoptosis rate significantly increased in cells after si RNA interference(〈0.05).·CONCLUSION:The decreased cell viability following AQP-1 down regulation is largely due to its induction of apoptosis of LECs.AQP-1 reduction might lead to changes of physiological functions in LECs,which might be associated with the occurrence and development of cataracts.
关 键 词:AQUAPORIN-1 small interfering RNA lensepithelial cells proliferation APOPTOSIS cell counting kit-8 flow cytometry
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