Departments of Pathology and Laboratory Medicine, University of Wisconsin, Madison, Wisconsin 53706, USA.
Mol Cell Proteomics. 2013 Jan;12(1):194-206. doi: 10.1074/mcp.M112.019745. Epub 2012 Oct 28.
Changes in the actin cytoskeleton, especially the formation of cross-linked actin networks (CLANs) are thought to contribute to the increased intraocular pressure observed in primary open-angle and steroid-induced glaucoma. To better understand the effects of glucocorticoids, we employed a shotgun method to analyze global changes in the cytoskeleton and integrin signaling pathways following dexamethasone (DEX) treatment of human trabecular meshwork (HTM) cells. RNA and cell lysates were obtained from HTM cells incubated with or without DEX. Changes in protein expression were determined by mass spectrometry (MS) following differential centrifugation of cell lysates to enrich for low-abundance cytoskeletal and signaling proteins, proteolytic digestion, and a titanium dioxide column to enrich for phosphopeptides. Results were validated by Western blots. Changes in RNA levels were determined with gene arrays and RT-PCR. Overall, MS identified 318 cytoskeleton associated proteins. Five of these proteins (PDLIM1, FGFR1OP, leiomodin-1, ZO-2 and LRP16A) were only detected in DEX-treated cells by MS. However, only PDLIM1 showed a statistically significant increase at the RNA level. Other proteins with differences at both the RNA and protein levels included β3 integrin, caveolin-1, Borg2, raftlin1, PI-3 kinase regulatory subunit α, transgelin, and filamin B. By immunofluorescence microscopy filamin B and PDLIM1 showed enhanced expression in human trabecular meshwork cells, but only PDLIM1 demonstrated significant localization within CLANs. Finally, MS showed that some of the cytoskeleton proteins (Borg2, leiomodin-1, LRP16A, raftlin1 and CKAP4) contained phosphorylated residues. This study suggests that DEX affects the expression of cytoskeleton proteins at the transcriptional and translational level and shows that a combined genomic and proteomic approach can be used for rapid analysis of proteins in the TM. It also shows that DEX altered the expression of components (PDLIM1 and β3 integrins) involved in CLAN formation and provides new findings into the effects of glucocorticoids on the cytoskeleton.
细胞骨架的变化,特别是交联肌动蛋白网络(CLANs)的形成,被认为是导致原发性开角型和类固醇诱导性青光眼患者眼内压升高的原因之一。为了更好地了解糖皮质激素的作用,我们采用鸟枪法分析了地塞米松(DEX)处理人眼小梁网(HTM)细胞后细胞骨架和整合素信号通路的整体变化。将 HTM 细胞与 DEX 孵育或不孵育,获得细胞裂解物的 RNA 和细胞裂解物。通过差异离心细胞裂解物以富集低丰度细胞骨架和信号蛋白、蛋白水解消化以及二氧化钛柱富集磷酸肽,然后通过质谱(MS)测定蛋白质表达的变化。通过 Western blot 验证结果。通过基因芯片和 RT-PCR 确定 RNA 水平的变化。总的来说,MS 鉴定了 318 种与细胞骨架相关的蛋白质。其中 5 种蛋白质(PDLIM1、FGFR1OP、leiomodin-1、ZO-2 和 LRP16A)仅通过 MS 在 DEX 处理的细胞中被检测到。然而,只有 PDLIM1 在 RNA 水平上显示出统计学上的显著增加。其他在 RNA 和蛋白质水平上都有差异的蛋白质包括β3 整合素、窖蛋白-1、Borg2、raftlin1、PI-3 激酶调节亚基 α、转胶蛋白和肌联蛋白 B。通过免疫荧光显微镜观察,发现 filamin B 和 PDLIM1 在人眼小梁网细胞中的表达增强,但只有 PDLIM1 显示在 CLANs 中有明显的定位。最后,MS 表明一些细胞骨架蛋白(Borg2、leiomodin-1、LRP16A、raftlin1 和 CKAP4)含有磷酸化残基。本研究表明,DEX 会影响细胞骨架蛋白的转录和翻译水平的表达,并表明基因组和蛋白质组学的联合方法可用于快速分析 TM 中的蛋白质。它还表明,DEX 改变了参与 CLAN 形成的成分(PDLIM1 和β3 整合素)的表达,并为糖皮质激素对细胞骨架的作用提供了新的发现。