Ben-Ze'ev A
Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Electrophoresis. 1996 Nov;17(11):1752-63. doi: 10.1002/elps.1150171113.
The morphology and functions of cells and tissues are determined, in a large part, by mechanical forces generated at cell-cell and cell-extracellular matrix (ECM) contacts. At these sites, transmembrane adhesion receptors of the integrin and cadherin families are linked, via their cytoplasmic domain, to the cytoskeleton by submembranal plaque proteins such as vinculin, alpha-actinin and the cell-cell junctional plaque proteins alpha- and beta-catenin and plakoglobin (or gamma-catenin). Recent studies have implicated this link of structural molecules between the outside and inside of the cell in signal transduction. We have shown that the expression of junctional plaque proteins is modulated during growth stimulation and differentiation, and is dramatically reduced in certain tumor cells. To study the functional significance of these changes in expression, we have used recombinant DNA technologies to overexpress or suppress the levels of junctional plaque proteins. In addition, we eliminated the expression of vinculin in embryonal stem (ES) cells and in the embryonal carcinoma F9 line by gene disruption employing homologous recombination. The results have indicated that moderate overexpression of cell-ECM plaque proteins results in reduced cell motility. In contrast, suppression of their expression, by antisense transfection, led to enhanced motility and conferred anchorage independent growth and tumorigenicity, upon injection into nude mice. These findings suggest that submembranal plaque proteins can act as effective tumor suppressors. In agreement with this notion, we found in several tumor cell lines diminished levels of junctional plaque proteins. Restoration of their level to that found in normal cells resulted in tumor suppression after their injection into experimental animals. Here we demonstrate the usefulness of the application of two dimensional (2-D) gel electrophoresis in these studies.
细胞和组织的形态及功能在很大程度上由细胞-细胞和细胞-细胞外基质(ECM)接触部位产生的机械力所决定。在这些部位,整合素家族和钙黏着蛋白家族的跨膜黏附受体通过其胞质结构域,经由诸如纽蛋白、α-辅肌动蛋白等膜下斑块蛋白以及细胞-细胞连接斑块蛋白α-连环蛋白、β-连环蛋白和桥粒斑珠蛋白(或γ-连环蛋白)与细胞骨架相连。最近的研究表明,这种细胞内外结构分子的连接参与了信号转导。我们已经证明,连接斑块蛋白的表达在生长刺激和分化过程中受到调节,并且在某些肿瘤细胞中显著降低。为了研究这些表达变化的功能意义,我们利用重组DNA技术来过表达或抑制连接斑块蛋白的水平。此外,我们通过同源重组基因敲除,消除了胚胎干细胞(ES细胞)和胚胎癌细胞F9系中纽蛋白的表达。结果表明,适度过表达细胞-ECM斑块蛋白会导致细胞运动性降低。相反,通过反义转染抑制它们的表达,则会增强细胞运动性,并赋予细胞在裸鼠体内注射后不依赖贴壁生长和致瘤性的能力。这些发现表明,膜下斑块蛋白可以作为有效的肿瘤抑制因子。与此观点一致,我们在几种肿瘤细胞系中发现连接斑块蛋白水平降低。将其水平恢复到正常细胞中的水平后,注射到实验动物体内会导致肿瘤抑制。在此,我们展示了二维(2-D)凝胶电泳在这些研究中的应用价值。