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首页> 外文期刊>The Journal of biological chemistry >The Lutheran/Basal Cell Adhesion Molecule Promotes Tumor Cell Migration by Modulating Integrin-mediated Cell Attachment to Laminin-511 Protein
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The Lutheran/Basal Cell Adhesion Molecule Promotes Tumor Cell Migration by Modulating Integrin-mediated Cell Attachment to Laminin-511 Protein

机译:通过调节整联蛋白介导的细胞附着于层粘连蛋白-511蛋白,路德兰/基础细胞粘附分子促进肿瘤细胞迁移

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摘要

Cell-matrix interactions are critical for tumor cell migration. Lutheran (Lu), also known as basal cell adhesion molecule (B-CAM), competes with integrins for binding to laminin α5, a subunit of LM-511, a major component of basement membranes. Here we show that the preferential binding of Lu/B-CAM to laminin α5 promotes tumor cell migration. The attachment of Lu/B-CAM transfectants to LM-511 was slightly weaker than that of control cells, and this was because Lu/B-CAM disturbed integrin binding to laminin α5. Lu/B-CAM induced a spindle cell shape with pseudopods and promoted cell migration on LM-511. In addition, blocking with an anti-Lu/B-CAM antibody led to a flat cell shape and inhibited migration on LM-511, similar to the effects of an activating integrin β1 antibody. We conclude that tumor cell migration on LM-511 requires that Lu/B-CAM competitively modulates cell attachment through integrins. We suggest that this competitive interaction is involved in a balance between static and migratory cell behaviors.
机译:细胞基质相互作用对于肿瘤细胞迁移至关重要。路德(LU),也称为基底细胞粘附分子(B-CAM),与整联蛋白竞争,用于与层粘蛋白α5结合,LM-511的亚基,基底膜的主要成分。在这里,我们表明LU / B型凸轮α5的优先结合促进了肿瘤细胞迁移。 Lu / B-CAM转染子于LM-511的附着比对照细胞略微弱,这是因为LU / B-CAM干扰与层粘蛋白α5的整合蛋白结合。 LU / B-CAM用假偶联诱导轴形细胞形状,并在LM-511上促进细胞迁移。另外,用抗LU / B-CAM抗体阻断导致平坦的细胞形状并抑制LM-511的迁移,类似于活化整合蛋白β1抗体的效果。我们得出结论,LM-511上的肿瘤细胞迁移要求LU / B-CAM通过整合素竞争地调节细胞附着。我们建议这种竞争性互动涉及静态和迁移细胞行为之间的平衡。

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