Save Sight Institute, The University of Sydney, NSW, Australia.
Save Sight Institute, The University of Sydney, NSW, Australia.
Exp Eye Res. 2018 Apr;169:122-133. doi: 10.1016/j.exer.2018.01.014. Epub 2018 Jan 31.
Recent studies indicate an important role for the transcriptional co-activator Yes-associated protein (YAP), and its regulatory pathway Hippo, in controlling cell growth and fate during lens development; however, the exogenous factors that promote this pathway are yet to be identified. Given that fibroblast growth factor (FGF)-signaling is an established regulator of lens cell behavior, the current study investigates the relationship between this pathway and Hippo/YAP-signaling during lens cell proliferation and fibre differentiation. Rat lens epithelial explants were cultured with FGF2 to induce epithelial cell proliferation or fibre differentiation. Immunolabeling methods were used to detect the expression of Hippo-signaling components, Total and Phosphorylated YAP, as well as fibre cell markers, Prox-1 and β-crystallin. FGF-induced lens cell proliferation was associated with a strong nuclear localisation of Total-YAP and low-level immuno-staining for phosphorylated-YAP. FGF-induced lens fibre differentiation was associated with a significant increase in cytoplasmic phosphorylated YAP (inactive state) and enhanced expression of core Hippo-signaling components. Inhibition of YAP with Verteporfin suppressed FGF-induced lens cell proliferation and ablated cell elongation during lens fibre differentiation. Inhibition of either FGFR- or MEK/ERK-signaling suppressed FGF-promoted YAP nuclear translocation. Here we propose that FGF promotes Hippo/YAP-signaling during lens cell proliferation and differentiation, with FGF-induced nuclear-YAP expression playing an essential role in promoting the proliferation of lens epithelial cells. An FGF-induced switch from proliferation to differentiation, hence regulation of lens growth, may play a key role in mediating Hippo suppression of YAP transcriptional activity.
最近的研究表明,转录共激活因子 Yes 相关蛋白 (YAP) 及其调节通路 Hippo 在控制晶状体发育过程中的细胞生长和命运方面发挥着重要作用;然而,促进这一途径的外源性因素尚未确定。鉴于成纤维细胞生长因子 (FGF) 信号是晶状体细胞行为的一个既定调节因子,本研究调查了该途径与 Hippo/YAP 信号在晶状体细胞增殖和纤维分化过程中的关系。用 FGF2 培养大鼠晶状体上皮外植体以诱导上皮细胞增殖或纤维分化。免疫标记方法用于检测 Hippo 信号成分、总 YAP 和磷酸化 YAP 以及纤维细胞标记物 Prox-1 和 β-晶状体蛋白的表达。FGF 诱导的晶状体细胞增殖与总 YAP 的强烈核定位和磷酸化 YAP 的低水平免疫染色有关。FGF 诱导的晶状体纤维分化与细胞质中磷酸化 YAP(失活状态)的显著增加和核心 Hippo 信号成分的增强表达有关。用 Verteporfin 抑制 YAP 可抑制 FGF 诱导的晶状体细胞增殖,并在晶状体纤维分化过程中消除细胞伸长。抑制 FGFR 或 MEK/ERK 信号均可抑制 FGF 促进的 YAP 核易位。在这里,我们提出 FGF 在晶状体细胞增殖和分化过程中促进 Hippo/YAP 信号,FGF 诱导的核 YAP 表达在促进晶状体上皮细胞增殖中起着至关重要的作用。从增殖到分化的 FGF 诱导转变,从而调节晶状体生长,可能在介导 Hippo 抑制 YAP 转录活性方面发挥关键作用。