Maddala Rupalatha, Reddy Venkat N, Epstein David L, Rao Vasantha
Department of Ophthalmology, Duke University Medical Center, Durham, NC, USA.
Mol Vis. 2003 Jul 17;9:329-36.
To determine the involvement of the Rho GTPases-mediated signaling pathway in growth factor-stimulated actomyosin cytoskeletal organization and focal adhesion formation in lens epithelial cells.
Serum starved human lens epithelial cells (SRA01/04) were treated with different growth factors including epidermal growth factor (EGF), basic-fibroblast growth factor (b-FGF), platelet derived growth factor (PDGF), transforming growth factor beta (TGF-beta), insulin-like growth factor 1 (IGF-1), lysophosphatidic acid (LPA), and thrombin. Growth factor stimulated activation of Rho and Rac GTPases were evaluated by GTP-loading pull-down assays. Changes in actin cytoskeletal organization and focal adhesions were determined by fluorescence staining using FITC-phalloidin and anti-vinculin antibody/rhodamine-conjugated secondary antibody, respectively. Fluorescence images were recorded using either confocal or fluorescence microscopy.
Rho GTPase activity was significantly augmented in human lens epithelial cells treated with EGF, b-FGF, TGF-beta, IGF-1, and LPA. Rac GTPase activation, in contrast, was significantly enhanced in response to only EGF or b-FGF. Serum starved human lens epithelial cells exhibited a strong increase in cortical actin stress fibers and integrin-mediated focal adhesions in response to b-FGF, PDGF, TGF-beta, thrombin, and LPA. While EGF induced a striking increase in membrane ruffling and a marginal increase on focal adhesion formation, IGF-1 had no effect on either. Pretreatment of lens epithelial cells with C3-exoenzyme (an irreversible inhibitor of Rho-GTPase), lovastatin (an isoprenylation inhibitor), or the Rho kinase inhibitor Y-27632 abolished the ability of the different growth factors to elicit actin stress fiber and focal adhesion formation. EGF induced membrane ruffling, however, was not suppressed by Y-27632 and C3-exoenzyme.
These results demonstrate that different growth factors induce actin cytoskeleton reorganization and formation of cell-ECM interactions in lens epithelial cells and this response of growth factors appears to be mediated, at least in part, through the Rho/Rho kinase-mediated signaling pathway. The ability of growth factors to trigger activation of Rho and Rac GTPases along with actomyosin cytoskeletal reorganization and formation of focal adhesions might well play a crucial role in lens epithelial cell proliferation, migration, elongation and survival.
确定Rho GTPases介导的信号通路在生长因子刺激晶状体上皮细胞中肌动球蛋白细胞骨架组织和粘着斑形成过程中的作用。
用血清饥饿处理人晶状体上皮细胞(SRA01/04),然后用不同的生长因子进行处理,包括表皮生长因子(EGF)、碱性成纤维细胞生长因子(b-FGF)、血小板衍生生长因子(PDGF)、转化生长因子β(TGF-β)、胰岛素样生长因子1(IGF-1)、溶血磷脂酸(LPA)和凝血酶。通过GTP加载下拉试验评估生长因子刺激的Rho和Rac GTPases的激活情况。分别使用FITC-鬼笔环肽和抗纽蛋白抗体/罗丹明偶联二抗进行荧光染色,以确定肌动蛋白细胞骨架组织和粘着斑的变化。使用共聚焦显微镜或荧光显微镜记录荧光图像。
在用EGF、b-FGF、TGF-β、IGF-1和LPA处理的人晶状体上皮细胞中,Rho GTPase活性显著增强。相比之下,仅在对EGF或b-FGF的反应中,Rac GTPase的激活显著增强。血清饥饿的人晶状体上皮细胞在对b-FGF、PDGF、TGF-β、凝血酶和LPA的反应中,皮质肌动蛋白应力纤维和整合素介导的粘着斑显著增加。虽然EGF诱导膜皱襞显著增加,粘着斑形成略有增加,但IGF-1对两者均无影响。用C3外切酶(一种Rho-GTPase的不可逆抑制剂)、洛伐他汀(一种异戊二烯化抑制剂)或Rho激酶抑制剂Y-27632预处理晶状体上皮细胞,可消除不同生长因子引发肌动蛋白应力纤维和粘着斑形成的能力。然而,Y-27632和C3外切酶并未抑制EGF诱导的膜皱襞。
这些结果表明,不同的生长因子诱导晶状体上皮细胞中的肌动蛋白细胞骨架重组和细胞与细胞外基质相互作用的形成,并且生长因子的这种反应似乎至少部分是通过Rho/Rho激酶介导的信号通路介导的。生长因子触发Rho和Rac GTPases激活以及肌动球蛋白细胞骨架重组和粘着斑形成的能力,很可能在晶状体上皮细胞的增殖、迁移、伸长和存活中起关键作用。