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The application of 3D micropatterning of agarose substrate for cell culture and in situ comet assays.

机译:琼脂糖底物的3D微图案化在细胞培养和原位彗星测定中的应用。

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We report the fabrication of a 3D micropatterned agarose substrate that enables the culture of single or multiple cells. Patterning was performed on dried agarose using deep UV irradiation leading to 6-microm-deep micropatterns of 25-70 microm in diameter. Cell adhesion was facilitated by the specific grafting of ECM (extra cellular matrix) proteins such as fibronectin into the micropatterns. We show that the pattern size induced the adhesion of one or more cells, thus allowing precise control of the cell number used in the assay, and that cells proliferated similarly as in standard culture conditions. Moreover, cell polarity appeared well preserved on this substrate, so polarized cells like hepatoma HepaRG cells might maintain their differentiation status and act as primary human hepatocytes for hepatotoxicity testing. These 3D patterned culture slides have been successfully used for in situ comet assays and there is evidence that the genotoxic effects of sub-cytotoxic concentrations of drugs could be analyzed in a large number of single HeLa cells. Coupled with the parallel-based design of the 3D micropatterning, which allows automated image analysis, these results strongly indicate that this new cell array system is suitable for high-throughput cytotoxicity and genotoxicity screening applications.
机译:我们报告制造的3D微图案琼脂糖底物,使单个或多个细胞的培养。使用深紫外辐射在干燥的琼脂糖上进行构图,从而形成直径为25-70微米的6微米深的微图案。通过将ECM(细胞外基质)蛋白(例如纤连蛋白)特异性移植到微模式中,可以促进细胞粘附。我们显示模式大小诱导了一个或多个细胞的粘附,因此可以精确控制测定中使用的细胞数,并且细胞的增殖与标准培养条件下的相似。此外,细胞极性似乎很好地保留在该底物上,因此极化细胞如肝癌HepaRG细胞可能保持其分化状态,并作为人类肝细胞进行肝毒性测试。这些3D图案化的培养玻片已成功用于原位彗星测定,并且有证据表明可以在大量单个HeLa细胞中分析亚细胞毒性浓度的药物的遗传毒性作用。这些结果与3D微图案的基于并行的设计相结合,可以进行自动图像分析,这些结果强烈表明,这种新的细胞阵列系统适用于高通量细胞毒性和遗传毒性筛选应用。

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