Iyengar Laxmi, Wang Qian, Rasko John E J, McAvoy John W, Lovicu Frank J
Save Sight Institute, University of Sydney, Sydney, NSW, Australia.
Differentiation. 2007 Sep;75(7):662-8. doi: 10.1111/j.1432-0436.2007.00167.x. Epub 2007 Mar 23.
The ocular environment is important for the establishment and maintenance of lens growth patterns and polarity. In the anterior chamber of the eye, the aqueous humour regulates lens epithelial cell proliferation whereas in the posterior, the vitreous humour regulates the differentiation of the lens cells into fiber cells. Members of the fibroblast growth factor (FGF) growth factor family have been shown to induce lens epithelial cells to undergo cell division and differentiate into fibers, with a low dose of FGF able to induce cell proliferation (but not fiber differentiation), and higher doses required to induce fiber differentiation. Both these cellular events have been shown to be regulated by the MAPK/ERK1/2 signalling pathway. In the present study, to better understand the contribution of ERK1/2 signalling in regulating lens cell proliferation and differentiation, we characterized the ERK1/2 signalling profiles induced by different doses of FGF, and compared these to those induced by the different ocular media. Here, we show that FGF induced a dose-dependent sustained activation of ERK1/2, with both a high (fiber differentiating) dose of FGF and vitreous, stimulating and maintaining a prolonged (up to 18 hr) ERK1/2 phosphorylation profile. In contrast, a lower (proliferating) dose of FGF, and aqueous, stimulated ERK1/2 phosphorylation for only up to 6 hr. If we selectively reduce the 18 hr ERK1/2 phosphorylation profile induced by vitreous to 6 hr, by specifically blocking FGF receptor signalling, the vitreous now fails to induce lens fiber differentiation but retains the ability to induce lens cell proliferation. These findings not only provide insights into the important role that FGF plays in the different ocular media that bathe the lens, but enlighten us on some of the putative molecular mechanisms by which one specific growth factor, in this case FGF, can elicit a different cellular response in the same cell type.
眼内环境对于晶状体生长模式和极性的建立与维持至关重要。在眼前房中,房水调节晶状体上皮细胞增殖,而在眼后段,玻璃体调节晶状体细胞向纤维细胞的分化。成纤维细胞生长因子(FGF)家族成员已被证明可诱导晶状体上皮细胞进行细胞分裂并分化为纤维细胞,低剂量的FGF能够诱导细胞增殖(但不能诱导纤维分化),而诱导纤维分化则需要更高剂量。这两种细胞事件均已证明受丝裂原活化蛋白激酶/细胞外信号调节激酶1/2(MAPK/ERK1/2)信号通路调控。在本研究中,为了更好地理解ERK1/2信号在调节晶状体细胞增殖和分化中的作用,我们对不同剂量FGF诱导的ERK1/2信号谱进行了表征,并将其与不同眼内介质诱导的信号谱进行比较。在此,我们表明FGF诱导ERK1/2呈剂量依赖性持续激活,高剂量(纤维分化)的FGF和玻璃体均刺激并维持延长(长达18小时)的ERK1/2磷酸化谱。相比之下,低剂量(增殖)的FGF和房水仅刺激ERK1/2磷酸化长达6小时。如果我们通过特异性阻断FGF受体信号,将玻璃体诱导的18小时ERK1/2磷酸化谱选择性地降低至6小时,此时玻璃体无法诱导晶状体纤维分化,但仍保留诱导晶状体细胞增殖的能力。这些发现不仅为FGF在环绕晶状体的不同眼内介质中所起的重要作用提供了见解,还让我们了解了一种特定生长因子(在本案例中为FGF)在同一细胞类型中引发不同细胞反应的一些假定分子机制。