Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.
Cell Transplant. 2012;21(2-3):411-20. doi: 10.3727/096368911X605312.
The de novo engineering of a uniform hepatocyte sheet in vitro is considered as a novel approach for liver-directed therapeutics. Hepatocytes can be cultured on a temperature-responsive culture dishes coated with poly(N-isopropylacrylamide) (PIPAAm). Following multiple days of culturing, the hepatocytes can be easily harvested as a uniform sheet by decreasing temperature from 37°C to 20°C. By modifying the sheet harvesting protocol, we have noticed that two different forms of the hepatocyte sheets, "extended" and "shrinking," were obtained. This study describes the methods for harvesting the two different forms of sheets, and their cellular structure and hepatocyte-specific functions. To obtain an "extended sheet" form, a cluster of hepatocytes covered with a support membrane was harvested by the temperature reduction. For the "shrinking sheet" form, the hepatocyte sheet was floated after reducing the culture temperature, and the floating process allowed the sheet to shrink spontaneously. Histological analysis revealed that the hepatocytes in the extended sheet form were predominantly flat, whereas the shrinking sheet contained cuboidal shaped hepatocytes. The preservation of hepatocyte-specific ultrastructures was confirmed in both types of sheets. To investigate hepatocyte-specific functionality, the harvested hepatocyte sheets were recultured on Matrigel-coated dishes. Assessment of protein production levels and chemical metabolizing activities showed the similar functionalities for each form. In contrast, the recalculation of these values per sheet versus per square centimeter of sheet surface demonstrated that the function of the shrinking sheet was significantly higher than that of the extended sheets. This study demonstrated that the hepatocyte sheets created on the PIPAAm dish could spontaneously shrink in size, but retain their hepatocyte functionality. This type of hepatocyte sheet could be utilized for the engineering of liver tissue in limited areas that are unable to give adequate transplant space.
体外从头设计均匀的肝细胞片被认为是一种用于肝脏定向治疗的新方法。肝细胞可以在涂有聚(N-异丙基丙烯酰胺)(PIPAAm)的温度响应培养皿上进行培养。经过多天的培养,通过将温度从 37°C 降低到 20°C,肝细胞可以很容易地作为均匀的片收获。通过修改片收获方案,我们注意到可以获得两种不同形式的肝细胞片,“扩展”和“收缩”。本研究描述了收获两种不同形式片的方法及其细胞结构和肝细胞特异性功能。为了获得“扩展片”形式,通过降低温度收获覆盖有支撑膜的肝细胞簇。对于“收缩片”形式,降低培养温度后,将肝细胞片浮起,并且浮起过程允许片自动收缩。组织学分析表明,在扩展片形式中的肝细胞主要是扁平的,而收缩片中包含立方体形的肝细胞。两种类型的片中均确认了保留了肝细胞特异性超微结构。为了研究肝细胞特异性功能,收获的肝细胞片在 Matrigel 涂覆的培养皿上再培养。评估蛋白质产生水平和化学代谢活性表明每种形式的功能相似。相比之下,将这些值按片计算与按片表面积计算的比值表明,收缩片的功能明显高于扩展片。本研究表明,在 PIPAAm 盘上创建的肝细胞片可以自发地缩小尺寸,但保留其肝细胞功能。这种类型的肝细胞片可用于在无法提供足够移植空间的有限区域中构建肝组织。