Sen Utpal, Moshal Karni S, Singh Mahavir, Tyagi Neetu, Tyagi Suresh C
Department of Physiology & Biophysics, HSC, University of Louisville School of Medicine, A-1215, 500 South Preston Street, Louisville, KY 40202, USA.
Mol Cell Biochem. 2007 Aug;302(1-2):133-43. doi: 10.1007/s11010-007-9435-4. Epub 2007 May 25.
Cellular cytoskeletal remodeling reflects alterations in local biochemical and mechanical changes in terms of stress that manifests relocation of signaling molecules within and across the cell. Although stretching due to load and chemical changes by high homocysteine (HHcy) causes cytoskeletal re-arrangement, the synergism between stretch and HHcy is unclear. We investigated the contribution of HHcy in cyclic stretch-induced focal adhesion (FA) protein redistribution leading to cytoskeletal re-arrangement in mouse aortic endothelial cells (MAEC). MAEC were subjected to cyclic stretch (CS) and HHcy alone or in combination. The redistribution of FA protein, and small GTPases were determined by Confocal microscopy and Western blot techniques in membrane and cytosolic compartments. We found that each treatment induces focal adhesion kinase (FAK) phosphorylation and cytoskeletal actin polymerization. In addition, CS activates and membrane translocates small GTPases RhoA with minimal effect on Rac1, whereas HHcy alone is ineffective in both GTPases translocation. However, the combined effect of CS and HHcy activates and membrane translocates both GTPases. Free radical scavenger NAC (N-Acetyl-Cysteine) inhibits CS and HHcy-mediated FAK phosphorylation and actin stress fiber formation. Interestingly, CS also activates and membrane translocates another FA protein, paxillin in HHcy condition. Cytochalasin D, an actin polymerization blocker and PI3-kinase inhibitor Wortmannin inhibited FAK phosphorylation and membrane translocation of paxillin suggesting the involvement of PI3K pathway. Together our results suggest that CS- and HHcy-induced oxidative stress synergistically contribute to small GTPase membrane translocation and focal adhesion protein redistribution leading to endothelial remodeling.
细胞细胞骨架重塑反映了局部生化和机械变化(即应力)的改变,这种改变表现为信号分子在细胞内和细胞间的重新定位。尽管由于负荷引起的拉伸以及高同型半胱氨酸(HHcy)导致的化学变化会引起细胞骨架重排,但拉伸与HHcy之间的协同作用尚不清楚。我们研究了HHcy在循环拉伸诱导的粘着斑(FA)蛋白重新分布中的作用,这种重新分布导致小鼠主动脉内皮细胞(MAEC)的细胞骨架重排。MAEC单独或联合接受循环拉伸(CS)和HHcy处理。通过共聚焦显微镜和蛋白质免疫印迹技术测定膜和胞质区室中FA蛋白和小GTP酶的重新分布。我们发现每种处理均诱导粘着斑激酶(FAK)磷酸化和细胞骨架肌动蛋白聚合。此外,CS激活并使小GTP酶RhoA膜转位,而对Rac1影响最小,而单独的HHcy对两种GTP酶的转位均无效。然而,CS和HHcy的联合作用激活并使两种GTP酶膜转位。自由基清除剂N-乙酰半胱氨酸(NAC)抑制CS和HHcy介导的FAK磷酸化和肌动蛋白应力纤维形成。有趣的是,在HHcy条件下,CS还激活并使另一种FA蛋白桩蛋白膜转位。细胞松弛素D(一种肌动蛋白聚合阻滞剂)和PI3激酶抑制剂渥曼青霉素抑制FAK磷酸化和桩蛋白的膜转位,提示PI3K途径参与其中。我们的结果共同表明,CS和HHcy诱导的氧化应激协同促进小GTP酶膜转位和粘着斑蛋白重新分布,从而导致内皮重塑。