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姜黄素通过抑制Wnt/β-连环蛋白信号通路激活来抑制角膜新生血管形成。

Suppression of corneal neovascularization by curcumin inhibition of Wnt/β-catenin pathway activation.

作者信息

Zhang Yong-Kang, Li Jing-Ming, Qin Li

机构信息

Department of Ophthalmology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, Shaanxi Province, China.

Department of Ophthalmology, Shaanxi Kangfu Hospital, Xi'an 710065, Shaanxi Province, China.

出版信息

Int J Ophthalmol. 2017 Dec 18;10(12):1791-1797. doi: 10.18240/ijo.2017.12.01. eCollection 2017.

Abstract

AIM

To investigate whether curcumin suppressed corneal neovascularization (CNV) formation inhibiting activation of Wnt/β-catenin pathway.

METHODS

Suture-induced CNV was established on Sprague-Dawley (SD) rats. Curcumin were daily administrated by subconjunctival injection. Phosphorylation of low-density lipoprotein receptor-related protein 6 (LRP6) and nuclear accumulation of β-catenin, two indicators of activated Wnt/β-catenin pathway, were determined by Western-blot analysis in subconfluent/proliferating human microvascular endothelial cells (HMEC) and neovascularized corneas. Wnt3a conditioned medium (WCM) were harvested from Wnt3a expressing cells. WCM-induced cell proliferation and endothelial tubular formation capacity was measured by MTT assay and Matrigel assay, respectively.

RESULTS

Phosphorylation of LRP6 and nuclear accumulation of β-catenin was significantly increased in subconfluent/proliferating endothelial cells. Activation of Wnt/β-catenin pathway by WCM markedly promotes HMEC proliferation and tubular formation. Curcumin inhibited LRP6 phosphorylation and nuclear accumulation of β-catenin. In addition, curcumin attenuated WCM-induced HMEC proliferation and disrupted tubular structure of endothelial cells on Matrigel. Meanwhile curcumin suppressed suture-induced CNV and inhibited LRP6 phosphorylation as well as β-catenin accumulation in SD rats.

CONCLUSION

Taken together, activation of Wnt/β-catenin pathway could be involved in endothelial proliferation during suture-induced CNV formation and curcumin attenuated CNV formation inhibition of Wnt/β-catenin pathway activation.

摘要

目的

研究姜黄素是否通过抑制Wnt/β-连环蛋白信号通路的激活来抑制角膜新生血管(CNV)形成。

方法

在Sprague-Dawley(SD)大鼠上建立缝线诱导的CNV模型。通过结膜下注射每日给予姜黄素。采用蛋白质免疫印迹法检测亚汇合/增殖期人微血管内皮细胞(HMEC)和新生血管化角膜中低密度脂蛋白受体相关蛋白6(LRP6)的磷酸化和β-连环蛋白的核内积聚,这两个指标用于评估Wnt/β-连环蛋白信号通路的激活情况。从表达Wnt3a的细胞中收集Wnt3a条件培养基(WCM)。分别采用MTT法和基质胶实验检测WCM诱导的细胞增殖和内皮细胞成管能力。

结果

在亚汇合/增殖期内皮细胞中,LRP6的磷酸化和β-连环蛋白的核内积聚显著增加。WCM激活Wnt/β-连环蛋白信号通路可显著促进HMEC增殖和成管。姜黄素可抑制LRP6磷酸化和β-连环蛋白的核内积聚。此外,姜黄素可减弱WCM诱导的HMEC增殖,并破坏基质胶上内皮细胞的管状结构。同时,姜黄素可抑制SD大鼠缝线诱导的CNV,并抑制LRP6磷酸化以及β-连环蛋白的积聚。

结论

综上所述,Wnt/β-连环蛋白信号通路的激活可能参与了缝线诱导的CNV形成过程中的内皮细胞增殖,而姜黄素通过抑制Wnt/β-连环蛋白信号通路的激活减弱了CNV的形成。

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