Save Sight Institute, University of Sydney, Sydney, New South Wales, Australia.
Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3599-610. doi: 10.1167/iovs.09-4797. Epub 2010 Feb 3.
PURPOSE. Although some of the factors and signaling pathways that are involved in induction of fiber differentiation have been defined, such as FGF-mediated MAPK/ERK and PI3-K/Akt signaling, the factors in the vitreous that regulate this differentiation process in vivo have yet to be identified. The purpose of this study was to better understand the role of growth factors in vitreous that regulate this process by further characterizing the signaling pathways involved in lens fiber differentiation. METHODS. Rat lens epithelial explants were used to compare the ability of vitreous, IGF-1, PDGF-A, EGF, and FGF-2 to stimulate the phosphorylation of ERK1/2 and Akt leading to fiber differentiation, in the presence or absence of selective receptor tyrosine kinase (RTK) inhibitors. RESULTS. Similar to vitreous, FGF induced a sustained ERK1/2 signaling profile, unlike IGF, PDGF, and EGF, which induced a more transient (shorter) activation of ERK1/2. For Akt activation, IGF was the only factor that induced a profile similar to vitreous. IGF, PDGF, and EGF potentiated the effects of a low dose of FGF on lens fiber differentiation by extending the duration of ERK1/2 phosphorylation. In the presence of selective RTK inhibitors, although the sustained vitreous-induced ERK1/2 signaling profile and subsequent fiber differentiation was perturbed, the results also showed that, although prolonged ERK1/2 phosphorylation was necessary, it was not sufficient for fiber differentiation to proceed. CONCLUSIONS. These results are consistent with FGF's being the key growth factor involved in vitreous-induced signaling leading to lens fiber differentiation; however, they also indicate that other vitreal growth factors such as IGF may be involved in fine-tuning ERK1/2- and Akt-phosphorylation to the level that is necessary for initiation and/or maintenance of lens fiber differentiation in vivo.
目的。虽然已经确定了一些参与纤维分化诱导的因素和信号通路,例如 FGF 介导的 MAPK/ERK 和 PI3-K/Akt 信号通路,但调节体内这种分化过程的玻璃体中的因素尚未确定。本研究的目的是通过进一步研究参与晶状体纤维分化的信号通路,更好地了解调节该过程的生长因子在玻璃体内的作用。
方法。使用大鼠晶状体上皮外植体比较玻璃体、IGF-1、PDGF-A、EGF 和 FGF-2 刺激 ERK1/2 和 Akt 磷酸化以诱导纤维分化的能力,同时存在或不存在选择性受体酪氨酸激酶 (RTK) 抑制剂。
结果。与玻璃体相似,FGF 诱导持续的 ERK1/2 信号通路谱,而不像 IGF、PDGF 和 EGF,它们诱导更短暂(更短)的 ERK1/2 激活。对于 Akt 激活,IGF 是唯一诱导类似于玻璃体的谱的因子。IGF、PDGF 和 EGF 通过延长 ERK1/2 磷酸化的持续时间,增强了低剂量 FGF 对晶状体纤维分化的作用。在存在选择性 RTK 抑制剂的情况下,尽管持续的玻璃体诱导的 ERK1/2 信号通路谱和随后的纤维分化受到干扰,但结果还表明,尽管延长 ERK1/2 磷酸化是必要的,但它不足以使纤维分化进行。
结论。这些结果与 FGF 是参与玻璃体诱导的信号通路导致晶状体纤维分化的关键生长因子一致;然而,它们还表明,其他玻璃体生长因子,如 IGF,可能参与微调 ERK1/2 和 Akt 磷酸化的水平,以满足体内晶状体纤维分化的起始和/或维持的需要。