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用于高密度肝细胞培养的微流体环境

Microfluidic environment for high density hepatocyte culture.

作者信息

Zhang Mimi Y, Lee Philip J, Hung Paul J, Johnson Terry, Lee Luke P, Mofrad Mohammed R K

机构信息

UCSF/UC Berkeley Joint Graduate Group in Bioengineering, Berkeley, CA, USA.

出版信息

Biomed Microdevices. 2008 Feb;10(1):117-21. doi: 10.1007/s10544-007-9116-9.

Abstract

We present a microfluidic bioreactor for culturing high-density arrays of hepatocytes in a tissue-like micro-architecture. The microfluidic environment mimicked physiological liver mass transport, enabling sustained culture of high density cells (>2,000 cells/mm(2)) without nutrient limitation for over 1 week. The key feature of this design was a microporous microfluidic barrier that formed a sieved-pocket to concentrate cells during loading. Nutrient depletion within the cell mass was avoided by maintaining a continuous flow of medium (10 microl/day) that diffused across the porous barrier. Human hepatoma cells (HepG2/C3A) remained viable and functional as demonstrated by fluorescent viability assays and secretion of albumin for the one-week culture period.

摘要

我们展示了一种微流控生物反应器,用于在类似组织的微结构中培养高密度肝细胞阵列。微流控环境模拟了生理性肝脏物质运输,能够在无营养限制的情况下持续培养高密度细胞(>2,000个细胞/mm²)超过1周。该设计的关键特征是一个微孔微流控屏障,在加载过程中形成一个筛状口袋来浓缩细胞。通过维持连续的培养基流(10微升/天)穿过多孔屏障,避免了细胞团内的营养耗尽。荧光活力测定和为期一周的培养期内白蛋白分泌证明,人肝癌细胞(HepG2/C3A)保持存活且功能正常。

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