Zhang Yong-Kang, Li Jing-Ming, Qin Li
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.
Int J Ophthalmol. 2017 Dec 18;10(12):1791-1797. doi: 10.18240/ijo.2017.12.01. eCollection 2017.
To investigate whether curcumin suppressed corneal neovascularization (CNV) formation inhibiting activation of Wnt/β-catenin pathway.
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.
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.
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.
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。
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。
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。
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。