Effects of resveratrol on ARPE-19 cell proliferation and migration via regulating the expression of proliferating cell nuclear antigen, P21,P27 and p38MAPK/MMP-9

AIM: To explore whether resveratrol (Res) can inhibit human retinal pigment epithelial cell (ARPE-19 cell) proliferation and migration, and to research the molecular mechanisms.METHODS: ARPE-19 cells were pretreated with various concentrations at 0, 50, 100, 150, 200 and 300 μmol/L of Res, and with...

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Veröffentlicht in:International journal of ophthalmology 2016-12, Vol.9 (12), p.1725-1731
Hauptverfasser: Hao, Xiao-Ning, Wang, Wen-Jie, Chen, Jian, Zhou, Qing, Qu, Yi-Xin, Liu, Xiao-Yong, Xu, Wei
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Sprache:eng
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Zusammenfassung:AIM: To explore whether resveratrol (Res) can inhibit human retinal pigment epithelial cell (ARPE-19 cell) proliferation and migration, and to research the molecular mechanisms.METHODS: ARPE-19 cells were pretreated with various concentrations at 0, 50, 100, 150, 200 and 300 μmol/L of Res, and with 0 μmol/L Res as the control for 24, 48 and 72h. The cell proliferation, apoptosis and migration were measured with cell counting kit-8 (CCK-8), flow cytometry, and wound-healing and Transwell assays, respectively. The expression of proliferating cell nuclear antigen (PCNA), P21 and P27, as well as matrix metalloproteinase-9 (MMP-9) and p38 mitogen-activated protein kinases (p38MAPK) was identified by Western blot.RESULTS: Cell proliferation was effectively inhibited by Res (P〈0.05). When pretreated with Res, cells arrested in S-phase increased remarkably (P〈0.05), but the apoptosis ratios showed no significant difference between the treatment and control groups (P〉0.05). Cell migration was suppressed by Res both in wound-healing assay and Transwell migration assay (P〈0.05). Decreases of PCNA, MMP-9 and p38MAPK, as well as increases of P21 and P27 were detected by Western blot (P〈0.05). CONCLUSION: Res can inhibit APRE-19 cell proliferation and migration in a concentration-dependent manner with up-regulation of the expression of P21 and P27, and down-regulation of PCNA, MMP-9 and p38MAPK.
ISSN:2222-3959
2227-4898
DOI:10.18240/ijo.2016.12.04