Schulz M W, Chamberlain C G, de Iongh R U, McAvoy J W
Department of Anatomy and Histology, University of Sydney, NSW Australia.
Development. 1993 May;118(1):117-26. doi: 10.1242/dev.118.1.117.
We have shown previously that FGF induces lens epithelial cells in explant culture to proliferate, migrate and differentiate into fibre cells in a progressive concentration-dependent manner. In situ, these processes occur in a distinct anterior-posterior pattern in clearly defined regions of the lens. Thus anterior-posterior differences in the bio-availability of FGF in the lens environment may play a role in determining lens polarity and growth patterns. In this study, using heparin chromatography and western blotting (or ELISA), we established that both acidic and basic FGF are present in the aqueous and vitreous (the ocular media that bathe the anterior and posterior compartments of the lens, respectively). In addition, substantially more FGF was recovered from vitreous than from aqueous. Both forms of FGF were also detected in lens fibre cells and capsule. A truncated form of basic FGF (less than 20 x 10(3) M(r)) predominated in every case with traces of higher M(r) forms in lens cells. For acidic FGF, the classical full-length form (about 20 x 10(3) M(r)) predominated in lens cells and a truncated form was found in vitreous. The capsule contained a higher M(r) form. Using our explant system, we also tested the biological activity of ocular media and FGF fractions obtained from vitreous and lens cells. Vitreous but not aqueous contained fibre-differentiating activity. Furthermore, virtually all the fibre-differentiating activity of vitreous was shown to be FGF-associated, as follows: (a) this activity remained associated with FGF during fractionation of vitreous by heparin and Mono-S chromatography and (b) the activity of the major FGF-containing fraction was blocked by antibodies to acidic and basic FGF. Posterior, but not anterior, capsule was shown to have mitogenic activity, which was neutralised by FGF antibodies and associated only with the cellular surface. These results support our hypothesis that FGF is involved in determining the behaviour of lens cells in situ. In particular, a key role for FGF in determining lens polarity and growth patterns is suggested by the anterior-posterior differences in the bio-availability of FGF in the ocular media and capsule.
我们之前已经表明,在器官培养中,成纤维细胞生长因子(FGF)能诱导晶状体上皮细胞增殖、迁移,并以浓度递增的方式逐步分化为纤维细胞。在体内,这些过程在晶状体明确界定区域内以前后模式清晰发生。因此,晶状体环境中FGF生物利用度的前后差异可能在决定晶状体极性和生长模式中发挥作用。在本研究中,我们通过肝素层析和蛋白质印迹法(或酶联免疫吸附测定)证实,酸性和碱性FGF均存在于房水和玻璃体中(分别为环绕晶状体前后腔的眼内介质)。此外,从玻璃体中回收的FGF比从房水中回收的要多得多。在晶状体纤维细胞和晶状体囊中也检测到了两种形式的FGF。在每种情况下,基本FGF的截短形式(分子量小于20×10³)占主导,在晶状体细胞中存在痕量的高分子量形式。对于酸性FGF,经典的全长形式(约20×10³分子量)在晶状体细胞中占主导,而在玻璃体中发现了截短形式。晶状体囊含有较高分子量形式。利用我们的器官培养系统,我们还测试了眼内介质以及从玻璃体和晶状体细胞中获得的FGF组分的生物活性。玻璃体而非房水含有纤维分化活性。此外,玻璃体几乎所有的纤维分化活性都显示与FGF相关,如下所示:(a)在通过肝素和单磺酸(Mono - S)层析对玻璃体进行分级分离过程中,该活性仍与FGF相关;(b)主要含FGF组分的活性被抗酸性和碱性FGF的抗体所阻断。晶状体后囊而非前囊显示具有促有丝分裂活性,该活性被FGF抗体中和且仅与细胞表面相关。这些结果支持了我们的假设,即FGF参与决定体内晶状体细胞的行为。特别是,眼内介质和晶状体囊中FGF生物利用度的前后差异表明FGF在决定晶状体极性和生长模式中起关键作用。