Erickson-Lamy K, Schroeder A, Epstein D L
Department of Ophthalmology, Harvard Medical School, Howe Laboratory of Ophthalmology, Boston, Massachusetts.
Invest Ophthalmol Vis Sci. 1992 Aug;33(9):2631-40.
Cell cultures derived from trabecular meshworks of human and bovine eyes and from bovine vascular endothelia were incubated at 37 degrees C for 1 hr with ethacrynic acid (ECA, 0.1-0.5 mmol/l) dissolved in culture medium. At 2 hr after the initial exposure, ECA at concentrations up to 0.4 mmol/l induced a reversible alteration in cell shape in all three cell types that was coincident with a change in the staining pattern of major cytoskeletal components including actin, alpha-actinin, vinculin, and vimentin. Distinct progressive alterations in beta-tubulin also occurred, with initial changes observed 10 min after ECA exposure. The ECA-induced changes in tubulin were blocked in part by preincubation with taxol (which stabilizes the microtubule structure), but they appeared to differ from those occurring with nocodazole (which interferes with tubulin assembly). These results suggest the possibility that ECA-induced increases in outflow facility may be mediated by alterations in the cytoskeletons of outflow pathway cells.
将来源于人眼和牛眼小梁网以及牛血管内皮的细胞培养物,在37℃下用溶解于培养基中的依他尼酸(ECA,0.1 - 0.5 mmol/L)孵育1小时。在初始暴露后2小时,浓度高达0.4 mmol/L的ECA在所有三种细胞类型中诱导了细胞形状的可逆改变,这与包括肌动蛋白、α - 辅肌动蛋白、纽蛋白和波形蛋白在内的主要细胞骨架成分染色模式的变化相一致。β - 微管蛋白也发生了明显的渐进性改变,在ECA暴露后10分钟观察到初始变化。预先用紫杉醇(可稳定微管结构)孵育可部分阻断ECA诱导的微管蛋白变化,但这些变化似乎与诺考达唑(干扰微管蛋白组装)引起的变化不同。这些结果提示,ECA诱导的房水流出易度增加可能由流出途径细胞细胞骨架的改变介导。