一种用于三维微组织工程的新型超薄胶原纳米层组装:用于长期稳定微流控肝细胞培养的逐层胶原沉积。

William J McCarty, O Berk Usta, Martha Luitje, Shyam Sundhar Bale, Abhinav Bhushan, Manjunath Hegde, Inna Golberg, Rohit Jindal, Martin L Yarmush
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引用次数: 20

摘要

利用细胞-基质相互作用创造稳定的肝细胞培养物在微设备中已被证明是困难的,因为尺寸限制限制了涉及使用水凝胶(如胶原蛋白“双凝胶”或“覆盖”)的经典组织培养技术的实用性。为了将胶原覆盖技术转化为微器件,我们利用琥珀酰化和甲基化反应对胶原进行修饰,制备了聚阴离子和聚阳离子的胶原溶液,并将其逐层沉积在肝细胞上,形成超薄的胶原纳米层。这些超薄胶原层覆盖在微装置中的肝细胞上,1)维持细胞形态、活力和极性,2)诱导胆小管形成和肌动蛋白重组,3)维持白蛋白和尿素分泌以及CYP活性,与平板培养中胶原双凝胶肝细胞中的肝细胞相似。除了直接应用该技术创建稳定的体外微流控肝细胞培养物用于药物毒性测试之外,该技术通常适用于其他3D微组织的薄生物材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A novel ultrathin collagen nanolayer assembly for 3-D microtissue engineering: Layer-by-layer collagen deposition for long-term stable microfluidic hepatocyte culture.

A novel ultrathin collagen nanolayer assembly for 3-D microtissue engineering: Layer-by-layer collagen deposition for long-term stable microfluidic hepatocyte culture.

A novel ultrathin collagen nanolayer assembly for 3-D microtissue engineering: Layer-by-layer collagen deposition for long-term stable microfluidic hepatocyte culture.

A novel ultrathin collagen nanolayer assembly for 3-D microtissue engineering: Layer-by-layer collagen deposition for long-term stable microfluidic hepatocyte culture.

The creation of stable hepatocyte cultures using cell-matrix interactions has proven difficult in microdevices due to dimensional constraints limiting the utility of classic tissue culture techniques that involve the use of hydrogels such as the collagen "double gel" or "overlay". To translate the collagen overlay technique into microdevices, we modified collagen using succinylation and methylation reactions to create polyanionic and polycationic collagen solutions, and deposited them layer-by-layer to create ultrathin collagen nanolayers on hepatocytes. These ultrathin collagen layers covered hepatocytes in microdevices and 1) maintained cell morphology, viability, and polarity, 2) induced bile canalicular formation and actin reorganization, and 3) maintained albumin and urea secretions and CYP activity similar to those observed in hepatocytes in collagen double gel hepatocytes in plate cultures. Beyond the immediate applications of this technique to create stable, in vitro microfluidic hepatocyte cultures for drug toxicity testing, this technique is generally applicable as a thin biomaterial for other 3D microtissues.

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来源期刊
TECHNOLOGY
TECHNOLOGY ENGINEERING, MULTIDISCIPLINARY-
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