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Chip-based Three-dimensional Cell Culture in Perfused Micro-bioreactors

机译:灌注式微生物反应器中基于芯片的三维细胞培养

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We have developed a chip-based cell culture system for the three-dimensional cultivation of cells. The chip is typically manufactured from non-biodegradable polymers, e.g., polycarbonate or polymethyl methacrylate by micro injection molding, micro hot embossing or micro thermoforming. But, it can also be manufactured from bio-degradable polymers. Its overall dimensions are 0.7 1 x 20 x 20 x 0.7 1 mm (h x w x l). The main features of the chips used are either a grid of up to 1156 cubic micro-containers (cf-chip) each the size of 120-300 x 300 x 300 μ (h x w x l) or round recesses with diameters of 300 μ and a depth of 300 μ (r-chip). The scaffold can house 10 Mio. cells in a three-dimensional configuration. For an optimal nutrient and gas supply, the chip is inserted in a bioreactor housing. The bioreactor is part of a closed steril circulation loop that, in the simplest configuration, is additionaly comprised of a roller pump and a medium reservoir with a gas supply. The bioreactor can be run in perfusion, superfusion, or even a mixed operation mode. We have successfully cultivated cell lines as well as primary cells over periods of several weeks. For rat primary liver cells we could show a preservation of organotypic functions for more than 2 weeks. For hepatocellular carcinoma cell lines we could show the induction of liver specific genes not or only slightly expressed in standard monolayer culture. The system might also be useful as a stem cell cultivation system since first differentiation experiments with stem cell lines were promising.
机译:我们已经开发了一种基于芯片的细胞培养系统,用于细胞的三维培养。芯片通常由不可生物降解的聚合物,例如聚碳酸酯或聚甲基丙烯酸甲酯,通过微注射成型,微热压花或微热成型来制造。但是,它也可以由可生物降解的聚合物制成。它的整体尺寸为0.7 1 x 20 x 20 x 0.7 1 mm(h xw x l)。所使用芯片的主要特征是每个网格尺寸为120-300 x 300 x 300μ(hxwxl)的多达1156立方微米的微容器(cf-chip)或直径为300μ,深度为300毫米的圆形凹槽300μ(r芯片)。脚手架可容纳10Mio。单元以三维配置。为了获得最佳的养分和气体供应,将芯片插入生物反应器外壳中。该生物反应器是一个封闭的灭菌循环回路的一部分,该循环在最简单的配置中还包括一个滚轴泵和一个带有气体供应的介质储存器。该生物反应器可以在灌注,灌注甚至混合操作模式下运行。我们已经成功培养了数周的细胞系以及原代细胞。对于大鼠原代肝细胞,我们可以显示器官型功能保留超过2周。对于肝癌细胞系,我们可以显示出在标准单层培养物中未表达或仅少量表达的肝特异性基因的诱导。该系统也可能用作干细胞培养系统,因为用干细胞系进行的首次分化实验很有希望。

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