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首页> 外文期刊>Lab on a chip >Multi-cellular 3D human primary liver cell culture elevates metabolic activity under fluidic flow
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Multi-cellular 3D human primary liver cell culture elevates metabolic activity under fluidic flow

机译:多细胞3D人类原代肝细胞培养可提高流体流动下的代谢活性

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We have developed a low-cost liver cell culture device that creates fluidic flow over a 3D primary liver cell culture that consists of multiple liver cell types, including hepatocytes and non-parenchymal cells (fibroblasts, stellate cells, and Kupffer cells). We tested the performance of the cell culture under fluidic flow for 14 days, finding that hepatocytes produced albumin and urea at elevated levels compared to static cultures. Hepatocytes also responded with induction of P450 (CYP1A1 and CYP3A4) enzyme activity when challenged with P450 inducers, although we did not find significant differences between static and fluidic cultures. Non-parenchymal cells were similarly responsive, producing interleukin 8 (IL-8) when challenged with 10 mu M bacterial lipoprotein (LPS). To create the fluidic flow in an inexpensive manner, we used a rocking platform that tilts the cell culture devices at angles between +/- 12 degrees, resulting in a periodically changing hydrostatic pressure drop between reservoirs and the accompanying periodically changing fluidic flow (average flow rate of 650 mu L min(-1), and a maximum shear stress of 0.64 dyne cm(-2)). The increase in metabolic activity is consistent with the hypothesis that, similar to unidirectional fluidic flow, primary liver cell cultures increase their metabolic activity in response to fluidic flow periodically changes direction. Since fluidic flow that changes direction periodically drastically changes the behavior of other cells types that are shear sensitive, our findings support the theory that the increase in hepatic metabolic activity associated with fluidic flow is either activated by mechanisms other than shear sensing (for example increased opportunities for gas and metabolite exchange), or that it follows a shear sensing mechanism that does not depend on the direction of shear. Our mode of device operation allows us to evaluate drugs under fluidic cell culture conditions and at low device manufacturing and operation costs.
机译:我们开发了一种低成本的肝细胞培养装置,该装置可在3D原代肝细胞培养上产生流体流动,该培养物由多种肝细胞类型组成,包括肝细胞和非实质细胞(成纤维细胞,星状细胞和库普弗细胞)。我们测试了流体在流体流下培养14天的性能,发现与静态培养相比,肝细胞产生的白蛋白和尿素水平升高。当用P450诱导剂攻击时,肝细胞还以P450酶(CYP1A1和CYP3A4)酶的诱导反应,尽管我们没有发现静态和流体培养之间的显着差异。非实质细胞也有类似反应,当用10μM细菌脂蛋白(LPS)攻击时会产生白介素8(IL-8)。为了以廉价的方式产生流体流,我们使用了一个摇动平台,该平台将细胞培养装置倾斜+/- 12度,从而导致储液器之间的流体静压降定期发生变化,并且流体流也随之发生变化(平均流量最大剪切应力为650μL min(-1),最大剪切应力为0.64达因cm(-2))。代谢活性的增加与以下假设相一致:与单向流体流动相似,原代肝细胞培养物响应于周期性变化的流体流动而增加了其代谢活性。由于周期性改变方向的流体流动会极大地改变其他对剪切敏感的细胞类型的行为,因此我们的发现支持以下理论:与流体流动相关的肝代谢活动的增加是由剪切感应以外的其他机制激活的(例如,机会增加) (用于气体和代谢物交换),或者遵循不依赖于剪切方向的剪切传感机制。我们的设备操作模式使我们能够在流体细胞培养条件下以及较低的设备制造和运营成本下评估药物。

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