首页> 外文期刊>Cell motility and the cytoskeleton >Dynamics of cell adhesion and motility in living cells is altered by a single amino acid change in E-cadherin fused to enhanced green fluorescent protein.
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Dynamics of cell adhesion and motility in living cells is altered by a single amino acid change in E-cadherin fused to enhanced green fluorescent protein.

机译:通过与增强型绿色荧光蛋白融合的E-cadherin中的单个氨基酸变化,可以改变活细胞中细胞粘附和运动的动力学。

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E-Cadherin regulates epithelial cell adhesion and is critical for the maintenance of tissue integrity. In sporadic diffuse-type gastric carcinoma, mutations of the E-cadherin gene are frequently observed that predominantly affect putative calcium binding motifs located in the linker region between the second and third extracellular domains. A single amino acid change (D370A) as found in a gastric carcinoma patient reduces cell adhesion and up-regulates cell motility. To study the effect of this mutation on the dynamics of cell adhesion and motility in living cells, enhanced green fluorescent protein (EGFP) was C-terminally fused to E-cadherin. The resulting mutant E-cadherin-EGFP fusion protein with a point mutation in exon 8 (p8-EcadEGFP) and a wild-type E-cadherin-EGFP fusion construct (wt-EcadEGFP) were expressed in human MDA-MB-435S cells. Fluorescent images were acquired by time-lapse laser scanning microscopy and E-cadherin was visualized during contact formation and in moving cells. Spatial and temporal localization of p8- and wt-EcadEGFP differed significantly. While wt-EcadEGFP was mainly localized at lateral membranes of contacting cells and formed E-cadherin puncta and plaques, p8-EcadEGFP-expressing cells frequently formed transient cell-cell contacts. During random cell migration, p8-EcadEGFP was found in lamellipodia. In contrast, wt-EcadEGFP localized at lateral cell-cell contact sites in low or non-motile cells. Inhibition of the epidermal growth factor (EGF) receptor, which plays a major role in lamellipodia formation and cell migration, reduced the motility of p8-EcadEGFP-expressing cells and caused lateral membrane staining of p8-EcadEGFP. Conversely, EGF induced cell motility and caused formation of lamellipodia that were E-cadherin positive. In conclusion, our data show that mutant E-cadherin significantly alters the dynamics of cell adhesion and motility in living cells and interferes with the formation of stable cell-cell contacts. Cell Motil. Cytoskeleton 59:50-61, 2004. Copyright 2004 Wiley-Liss, Inc.
机译:E-钙黏着蛋白调节上皮细胞粘附,对于维持组织完整性至关重要。在散发性弥漫型胃癌中,经常观察到E-钙粘着蛋白基因的突变,这些突变主要影响位于第二个和第三个细胞外结构域之间的接头区域中的假定钙结合基序。在胃癌患者中发现的单个氨基酸变化(D370A)会降低细胞黏附并上调细胞运动性。为了研究此突变对活细胞中细胞粘附和运动的动力学的影响,将增强的绿色荧光蛋白(EGFP)C端融合到E-钙粘蛋白上。在人MDA-MB-435S细胞中表达所得的外显子8具有点突变的突变E-钙粘着蛋白-EGFP融合蛋白(p8-EcadEGFP)和野生型E-钙粘着蛋白-EGFP融合构建体(wt-EcadEGFP)。通过延时激光扫描显微镜获得荧光图像,并在接触形成过程中和在移动的细胞中可视化E-钙粘着蛋白。 p8-和wt-EcadEGFP的时空定位差异显着。虽然wt-EcadEGFP主要位于接触细胞的侧膜并形成E-钙粘蛋白点和斑块,但表达p8-EcadEGFP的细胞经常形成瞬时细胞与细胞的接触。在随机细胞迁移过程中,在lamellipodia中发现了p8-EcadEGFP。相反,wt-EcadEGFP位于低或非运动细胞的横向细胞-细胞接触位点。表皮生长因子(EGF)受体的抑制作用,在片状脂蛋白形成和细胞迁移中起主要作用,降低了表达p8-EcadEGFP的细胞的运动,并引起p8-EcadEGFP的侧膜染色。相反,EGF诱导细胞运动,并导致E-cadherin阳性的片状脂蛋白形成。总之,我们的数据表明,突变型E-钙粘着蛋白显着改变了活细胞中细胞粘附和运动的动力学,并干扰了稳定的细胞间接触。细胞动力。 Cytoskeleton 59:50-61,2004。版权所有2004 Wiley-Liss,Inc.。

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