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Krüppel-like factor 4 mediates cellular migration and invasion by altering RhoA activity

机译:Krüppel样因子4通过改变RhoA活性介导细胞迁移和侵袭

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AbstractKru¨ppel like factor 4 (KLF4) is a transcription factor that regulates genes related to differentiation and proliferation. KLF4 also plays a role in metastasis via epithelial to mesenchymal transition. Here, we investigate the function of Klf4 in migration and invasion using mouse embryonic fibroblasts and the RKO human colon cancer cell line. Compared to wild-type, cells lacking Klf4 exhibited increased migration-associated phenotypes. In addition, overexpression of Klf4 in Klf4?/? MEFs attenuated the presence of stress fibers to wild-type levels. An invasion assay suggested that lack of Klf4 resulted in increased invasive capacity. Finally, analysis of RhoA showed elevated RhoA activity in both RKO and MEF cells. Taken together, our results strongly support the novel role of KLF4 in a post-translational regulatory mechanism where KLF4 indirectly modulates the actin cytoskeleton morphology via activity of RhoA in order to inhibit cellular migration and invasion.
机译:摘要克虏伯样因子4(KLF4)是一种转录因子,可调节与分化和增殖相关的基因。 KLF4在上皮到间充质转移的转移中也起作用。在这里,我们调查使用小鼠胚胎成纤维细胞和RKO人结肠癌细胞系在迁移和侵袭中Klf4的功能。与野生型相比,缺少Klf4的细胞表现出增加的与迁移相关的表型。另外,在Klf4α/β中Klf4的过表达。 MEF将应力纤维的存在衰减至野生型水平。侵袭试验表明缺乏Klf4导致侵袭能力增加。最后,RhoA分析显示RKO和MEF细胞中RhoA活性均升高。两者合计,我们的结果强烈支持KLF4在翻译后调节机制中的新作用,其中KLF4通过RhoA的活性间接调节肌动蛋白的细胞骨架形态,以抑制细胞迁移和侵袭。

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