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Regulation of chemokine receptor CXCR4 in HepG2 cell adhesion sensing by QCM

机译:QCM对HepG2细胞粘附传感中趋化因子受体CXCR4的调节。

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Cell adhesion is implicated in a number of biological pathways such as angiogenesis, arteriosclerosis, chronic inflammatory diseases, and carcinogenesis. Chemokine receptor CXCR4 is often found aberrantly expressed on metastatic tumor cells. To investigate CXCR4 signaling in tumor cell adhesion, we stably overexpressed CXCR4 in hepatocellular carcinoma HepG2 cells. Regulation of CXCR4 in HepG2 cell adhesion was in-situ investigated using a quartz crystal microbalance. The results of cell adhesion assays illustrated that stimulation of the receptor with its ligand, CXCL12, promotes adhesion of HepG2-CXCR4 cells to both extracellular matrix and endothelial ligands.
机译:细胞粘附与许多生物学途径有关,例如血管生成,动脉硬化,慢性炎性疾病和致癌作用。通常发现趋化因子受体CXCR4在转移性肿瘤细胞上异常表达。为了研究肿瘤细胞粘附中的CXCR4信号传导,我们在肝细胞癌HepG2细胞中稳定地过度表达了CXCR4。使用石英晶体微量天平就地研究了HepG2细胞粘附中CXCR4的调控。细胞粘附测定的结果表明,用其配体CXCL12刺激受体可促进HepG2-CXCR4细胞与细胞外基质和内皮配体的粘附。

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