Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>

AIM: To investigate the effects of Aflibercept on the K<sup>+</sup> channel of retinal Müller cell membrane cultured <i>in vitro</i>.<p>METHODS: Human Müller cells were divided into 3 groups(control group, high glucose group and experimental group). The control group we...

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Main Authors: Qi-Feng Lei, Wei Cai
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2019-04-01
Series:Guoji Yanke Zazhi
Subjects:
Online Access:http://ies.ijo.cn/cn_publish/2019/4/201904004.pdf
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author Qi-Feng Lei
Wei Cai
author_facet Qi-Feng Lei
Wei Cai
author_sort Qi-Feng Lei
collection DOAJ
description AIM: To investigate the effects of Aflibercept on the K<sup>+</sup> channel of retinal Müller cell membrane cultured <i>in vitro</i>.<p>METHODS: Human Müller cells were divided into 3 groups(control group, high glucose group and experimental group). The control group were cultured in conventional DMEM medium; the high glucose group were cultured in high glucose DMEM medium; the experimental group were cultured with high glucose DMEM medium and 100μmol/L Aflibercept, and the K<sup>+</sup> concentration of the cells were detected by MQAE, and the cell survival were detected by MTT assay, the flow cytometry were used to detect apoptosis rates, Western blot analysis were used to detect the Müller cell caspase-3 protein levels.<p>RESULTS: The Müller cells were positive for glutamine synthetase(GS)after 48h of culture, and the purification degree were above 90%. The relative concentrations of K<sup>+</sup> in the control group, high glucose group and experimental group were(2.14±0.44)%,(23.11±4.39)%,(5.20±0.92)%, and cell viability were(100.00±0.00)%, respectively(73.24±4.13)%,(85.22±5.33)%, the apoptosis rates were(5.03±1.91)%,(26.73±3.14)%,(16.63±2.73)%, and compared the differences between two groups were statistically significant(<i>P</i><0.05). Compared with the control group, the level of caspase-3 protein in the high glucose group Müller cells were increased significantly(<i>P</i><0.05); compared with the high glucose group Müller cells, the caspase-3 protein level in the experimental group Müller cells were decreased significantly(<i>P</i><0.05).<p>CONCLUSION: Aflibercept can inhibit the K<sup>+</sup> channel of retinal Müller cells <i>in vitro</i>, inhibit the apoptosis of Müller cells induced by high glucose, decrease the expression of caspase-3 protein, and promote cell proliferation.
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spelling doaj.art-b1aec69759304403891ce3f0bc75b8b92022-12-21T18:41:58ZengPress of International Journal of Ophthalmology (IJO PRESS)Guoji Yanke Zazhi1672-51231672-51232019-04-0119454755010.3980/j.issn.1672-5123.2019.4.04Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>Qi-Feng Lei0Wei Cai1Department of Ophthalmology, Dongfeng Hospital Affiliated to Hubei University of Medicine, Shiyan 442000, Hubei Province, ChinaDepartment of Ophthalmology, Dongfeng Hospital Affiliated to Hubei University of Medicine, Shiyan 442000, Hubei Province, ChinaAIM: To investigate the effects of Aflibercept on the K<sup>+</sup> channel of retinal Müller cell membrane cultured <i>in vitro</i>.<p>METHODS: Human Müller cells were divided into 3 groups(control group, high glucose group and experimental group). The control group were cultured in conventional DMEM medium; the high glucose group were cultured in high glucose DMEM medium; the experimental group were cultured with high glucose DMEM medium and 100μmol/L Aflibercept, and the K<sup>+</sup> concentration of the cells were detected by MQAE, and the cell survival were detected by MTT assay, the flow cytometry were used to detect apoptosis rates, Western blot analysis were used to detect the Müller cell caspase-3 protein levels.<p>RESULTS: The Müller cells were positive for glutamine synthetase(GS)after 48h of culture, and the purification degree were above 90%. The relative concentrations of K<sup>+</sup> in the control group, high glucose group and experimental group were(2.14±0.44)%,(23.11±4.39)%,(5.20±0.92)%, and cell viability were(100.00±0.00)%, respectively(73.24±4.13)%,(85.22±5.33)%, the apoptosis rates were(5.03±1.91)%,(26.73±3.14)%,(16.63±2.73)%, and compared the differences between two groups were statistically significant(<i>P</i><0.05). Compared with the control group, the level of caspase-3 protein in the high glucose group Müller cells were increased significantly(<i>P</i><0.05); compared with the high glucose group Müller cells, the caspase-3 protein level in the experimental group Müller cells were decreased significantly(<i>P</i><0.05).<p>CONCLUSION: Aflibercept can inhibit the K<sup>+</sup> channel of retinal Müller cells <i>in vitro</i>, inhibit the apoptosis of Müller cells induced by high glucose, decrease the expression of caspase-3 protein, and promote cell proliferation.http://ies.ijo.cn/cn_publish/2019/4/201904004.pdfretinaMüller cellsmembrane ion channelAflibercept
spellingShingle Qi-Feng Lei
Wei Cai
Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>
Guoji Yanke Zazhi
retina
Müller cells
membrane ion channel
Aflibercept
title Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>
title_full Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>
title_fullStr Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>
title_full_unstemmed Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>
title_short Effects of Aflibercept on ion channel of retinal Müller cell membrane cultured <i>in vitro</i>
title_sort effects of aflibercept on ion channel of retinal muller cell membrane cultured i in vitro i
topic retina
Müller cells
membrane ion channel
Aflibercept
url http://ies.ijo.cn/cn_publish/2019/4/201904004.pdf
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