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姜黄素纳米颗粒对人视网膜色素上皮细胞增殖及血管内皮生长因子表达的影响

Effects of curcumin nanoparticles on proliferation and VEGF expression of human retinal pigment epithelial cells.

作者信息

Zheng Hai-Sheng, Lan Yu-Qing, Zhong Xing-Wu, Zhou Huai-Sheng, Xu Jia-Yao

机构信息

Hainan Eye Hospital and Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Haikou 570311, Hainan Province, China.

Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, Guangdong Province, China.

出版信息

Int J Ophthalmol. 2022 Jun 18;15(6):905-913. doi: 10.18240/ijo.2022.06.07. eCollection 2022.

DOI:10.18240/ijo.2022.06.07
PMID:35814903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9203465/
Abstract

AIM

To investigate the effects of curcumin (Cur) nanoparticles loaded with chitosan derivatives grafted by deoxycholic acid (Chit-DC) on human retinal pigment epithelial (hRPE) cell proliferation and vascular endothelial growth factor (VEGF) mRNA expression.

METHODS

Cur nanoparticles were synthesized with Chit-DC as the carrier and Cur as the supported drug. Cell counting kit-8 (CCK-8) method was used to detect the effects of different concentrations of Cur/Chit-DC, Chit-DC, and Cur on the proliferation of hRPE cells for different times. The changes of Cur/Chit-DC and Cur on hRPE cell cycle were determined by flow cytometry. Semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) was used to detect the mRNA expression levels of VEGF in hRPE cells treated with Cur, Chit-DC and Cur/Chit-DC at 10 µg/mL for 24h.

RESULTS

Different concentrations of Chit-DC nanoparticle treated hRPE cells had no significant difference in terms of optical density (OD) values compared with the control group at 24h and 48h. Moreover, there was no change in the cell morphology under a light microscope. After 24h treatment with Cur/Chit-DC and Cur, the percentage of G0-G1 phase cells increased and the percentage of S phase cells decreased in all concentration groups. Cur/Chit-DC and Cur in all concentration groups inhibited the proliferation of hRPE cells in a time and dose dependent manner, and reduced the expression level of VEGF mRNA.

CONCLUSION

The Cur/Chit-DC nanoparticles can release Cur continuously and have sustained release function. Both Cur/Chit-DC nanoparticles and Cur could inhibit hRPE cells cultured , and could reduce the expression level of VEGF mRNA in hRPE cells.

摘要

目的

研究载有经脱氧胆酸接枝的壳聚糖衍生物(Chit-DC)的姜黄素(Cur)纳米颗粒对人视网膜色素上皮(hRPE)细胞增殖及血管内皮生长因子(VEGF)mRNA表达的影响。

方法

以Chit-DC为载体、Cur为载药合成Cur纳米颗粒。采用细胞计数试剂盒-8(CCK-8)法检测不同浓度的Cur/Chit-DC、Chit-DC和Cur在不同时间对hRPE细胞增殖的影响。通过流式细胞术测定Cur/Chit-DC和Cur对hRPE细胞周期的影响。采用半定量逆转录-聚合酶链反应(RT-PCR)检测用10μg/mL的Cur、Chit-DC和Cur/Chit-DC处理24小时的hRPE细胞中VEGF的mRNA表达水平。

结果

在24小时和48小时时,不同浓度的Chit-DC纳米颗粒处理的hRPE细胞与对照组相比,光密度(OD)值无显著差异。此外,光学显微镜下细胞形态无变化。用Cur/Chit-DC和Cur处理24小时后,所有浓度组的G0-G1期细胞百分比增加,S期细胞百分比降低。所有浓度组的Cur/Chit-DC和Cur均以时间和剂量依赖性方式抑制hRPE细胞增殖,并降低VEGF mRNA的表达水平。

结论

Cur/Chit-DC纳米颗粒可持续释放Cur并具有缓释功能。Cur/Chit-DC纳米颗粒和Cur均可抑制培养的hRPE细胞,并可降低hRPE细胞中VEGF mRNA的表达水平。