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Regulation of Chemokine Receptor CXCR4 in HepG2 Cell Adhesion Sensing by QCM

机译:QCM调节趋化因子受体CXCR4在QCM中的HepG2细胞粘附性感测

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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:细胞粘附涉及许多生物途径,例如血管生成,动脉硬化,慢性炎症疾病和致癌作用。趋化因子受体CXCR4通常在转移性肿瘤细胞上发现异常表达。为了探讨肿瘤细胞粘附中的CXCR4信号传导,我们在肝细胞癌HepG2细胞中稳定地过表达CXCR4。使用石英晶体微稳定调查HepG2细胞粘附中CXCR4的调节。细胞粘附测定的结果表明,通过其配体CXCl12刺激受体促进HepG2-CXCR4细胞对细胞外基质和内皮配体的粘附性。

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