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Inhibiting Cell Viability and Motility by Layer-by-Layer Assembly and Biomineralization

机译:通过层逐层组装和生物矿化抑制细胞活力和运动

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Herein, we proposed a drug-free strategy named cell surface shellization to inhibit the motility of SKOV-3 and HeLa cells. We alternately deposited two- or three-layer cationic polyelectrolyte (PE) and anionic PE films on the surface of SKOV-3 and HeLa cells. Then, a mineral shell (calcium carbonate, CaCO_(3)) was formed on the surface of polymer shells via electrostatic force and biomineralization. The CCK-8 assay results and live/dead staining showed that the surface shells strongly aggravated the cytotoxicity. The monolayer scratch wound migration assay results and immunofluorescence staining results showed that the shells, especially the mineral shells, could efficiently inhibit the migration of SKOV-3 and HeLa cells without any anticancer drugs. The immunofluorescence results of the three small G proteins of the cells showed that the immunofluorescence intensity in SKOV-3 did not change. Preliminary results from our laboratory showed an increase in MMP-9 secreted by cancer cells after coating with films or mineral shells. It suggests that mechanisms that inhibit cell migration are related to the MMP signaling pathway. All the results indicated that shellization (films or nanomineral shells) but not limited to calcification can be used as one of the tools to change the function of cells.
机译:在此,我们提出了一种名为细胞表面壳的无毒策略,以抑制Skov-3和HeLa细胞的运动性。我们在skov-3和HeLa细胞的表面上交替地沉积了两层或三层阳离子聚电解质(PE)和阴离子PE膜。然后,在聚合物壳的表面上通过静电力和生物碳化形成矿物壳(碳酸钙,CaCO_(3))。 CCK-8测定结果和活/死染色表明,表面壳强烈加剧了细胞毒性。单层刮伤伤口迁移测定结果和免疫荧光染色结果表明,壳体,尤其是矿物壳,可以有效地抑制Skov-3和HeLa细胞的迁移而没有任何抗癌药物。细胞的三个小G蛋白的免疫荧光结果表明Skov-3中的免疫荧光强度没有变化。我们实验室的初步结果表明,用薄膜或矿物壳涂覆后,癌细胞分泌的MMP-9增加。它表明,抑制细胞迁移的机制与MMP信号通路有关。所有结果表明,壳化(薄膜或薄膜或纳米壳)但不限于钙化,可以用作改变细胞功能的工具之一。

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