Huang Jian-Xin, Feldmeier Mary, Shui Ying-Bo, Beebe David C
Department of Ophthalmology and Visual Sciences, Cataract Research Center, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Invest Ophthalmol Vis Sci. 2003 Feb;44(2):680-90. doi: 10.1167/iovs.01-1177.
Previous studies have implicated members of the fibroblast growth factor (FGF) and insulin-like growth factor (IGF) families as stimulators of lens fiber cell differentiation in rodent and chicken embryo lenses, respectively. In the present study, the role of FGFs in fiber cell differentiation and epithelial cell proliferation in chicken embryos was examined.
Lenses were injected on embryonic day (E)3 with replication-defective retroviruses that express full-length or truncated FGF receptor (FGFR)-1 or a secreted form of FGF1. Lens epithelial explants were cultured in defined medium or medium supplemented with FGFs or vitreous humor, in the presence or absence of the FGF receptor antagonist SU5402. Explants were also cultured in vitreous humor that had been depleted of heparin-binding growth factors. Cell elongation was measured optically and protein accumulation by densitometry and Western blot analysis.
Lens fiber cell differentiation was not inhibited in cells infected with virus expressing truncated FGFR1. Epithelial cells infected with virus encoding a secreted form of FGF1 did not differentiate into ectopic fiber cells. Viral transduction of FGFR1, truncated FGFR1, or FGF1 did not appreciably alter the proliferation of lens epithelial cells. Bovine vitreous humor stimulated chicken embryo lens epithelial cells to elongate and express markers of lens fiber cell differentiation. Bovine vitreous humor, but not FGF2, protected lens epithelial cells from apoptosis. Depleting vitreous humor of heparin-binding growth factors or treatment of lens cells with SU5402 did not inhibit the initial, rapid phase of lens cell elongation. Both treatments, used separately or together, reduced but did not prevent the expression of later markers of fiber cell differentiation.
Fiber differentiation factors that are not members of the FGF family are present in chicken and mammalian vitreous humor. The factors that stimulate fiber cell differentiation in avian and mammalian eyes are similar.
先前的研究表明,成纤维细胞生长因子(FGF)家族和胰岛素样生长因子(IGF)家族的成员分别是啮齿动物和鸡胚晶状体中晶状体纤维细胞分化的刺激因子。在本研究中,检测了FGFs在鸡胚纤维细胞分化和上皮细胞增殖中的作用。
在胚胎第3天(E3)向晶状体注射表达全长或截短型FGF受体(FGFR)-1的复制缺陷型逆转录病毒或分泌形式的FGF1。晶状体上皮外植体在限定培养基或补充有FGFs或玻璃体液的培养基中培养,同时存在或不存在FGF受体拮抗剂SU5402。外植体也在已去除肝素结合生长因子的玻璃体液中培养。通过光学方法测量细胞伸长,并通过光密度测定和蛋白质印迹分析测量蛋白质积累。
感染表达截短型FGFR1的病毒的细胞中,晶状体纤维细胞分化未受抑制。感染编码分泌形式FGF1的病毒的上皮细胞未分化为异位纤维细胞。FGFR1、截短型FGFR1或FGF1的病毒转导并未明显改变晶状体上皮细胞的增殖。牛玻璃体液刺激鸡胚晶状体上皮细胞伸长并表达晶状体纤维细胞分化标志物。牛玻璃体液而非FGF2可保护晶状体上皮细胞免于凋亡。去除玻璃体液中的肝素结合生长因子或用SU5402处理晶状体细胞,均未抑制晶状体细胞伸长的初始快速阶段。单独或联合使用这两种处理方法均可减少但不能阻止纤维细胞分化后期标志物的表达。
鸡和哺乳动物的玻璃体液中存在非FGF家族成员的纤维分化因子。鸟类和哺乳动物眼睛中刺激纤维细胞分化的因子相似。