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

机译:用于3-D微组织工程的新型超薄胶原蛋白纳米层组件:胶原蛋白的逐层沉积可长期稳定地进行微流体肝细胞培养

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摘要

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.
机译:由于尺寸限制,限制了经典组织培养技术的实用性,在微型设备中使用细胞-基质相互作用创建稳定的肝细胞培养物已被证明是困难的,经典组织培养技术的使用涉及水凝胶的使用,例如胶原蛋白“双重凝胶”或“覆盖”。为了将胶原蛋白覆盖技术转化为微设备,我们使用琥珀酰化和甲基化反应修饰了胶原蛋白,以创建聚阴离子和聚阳离子胶原蛋白溶液,并将它们逐层沉积,从而在肝细胞上形成了超薄的胶原蛋白纳米层。这些超薄胶原层覆盖了微型设备中的肝细胞,1)维持细胞形态,活力和极性,2)诱导胆管形成和肌动蛋白重组,3)维持白蛋白和尿素分泌以及CYP活性类似于在双胶原肝细胞中观察到的平板培养中的凝胶肝细胞。除了该技术的立即应用以外,它还可以创建稳定的,在体外用于药物毒性测试的>体外微流体肝细胞培养物,该技术通常还可以用作其他3D微型组织的薄生物材料。

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