Zhu Xin Hao, Wang Chi-Hwa, Tong Yen Wah
Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore 119260.
J Biomed Mater Res B Appl Biomater. 2007 Jul;82(1):7-16. doi: 10.1002/jbm.b.30698.
In this study, an oil-in-water emulsion solvent evaporation technique was used to fabricate poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV, 8% PHV), microspheres as scaffold, to guide liver cell growth. Human hepatoma cell lines, HepG2 and Hep3B, were cultured in vitro on both the microspheres and polymer films. SEM and optical microscope images showed that multilayer cells were formed among the microspheres to bridge them together and developed into cell-construct aggregates after 1 week of culture. MTT results showed that the cell proliferation on the microspheres was more than two times higher than that on the films after 12 days of culture. The cells seeded on microspheres secreted albumin 2-4 times more than that on the positive control after 1 week of culture, which indicated that this hepatic function was greatly improved by the aggregation of cells on microspheres. Although HepG2 failed to express P-450 activity, this hepatic function was preserved when Hep3B cultured on microspheres. All the results indicated that PHBV microspheres are appropriate scaffolds for liver tissue engineering.
在本研究中,采用水包油乳液溶剂蒸发技术制备聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV,8% PHV)微球作为支架,以引导肝细胞生长。人肝癌细胞系HepG2和Hep3B在微球和聚合物膜上进行体外培养。扫描电子显微镜(SEM)和光学显微镜图像显示,培养1周后,微球之间形成了多层细胞将它们连接在一起,并发展成细胞构建聚集体。噻唑蓝(MTT)结果表明,培养12天后,微球上的细胞增殖比膜上的细胞增殖高两倍多。培养1周后,接种在微球上的细胞分泌白蛋白的量比阳性对照上的细胞多2-4倍,这表明微球上细胞的聚集极大地改善了肝功能。尽管HepG2未能表达P-450活性,但当Hep3B在微球上培养时,这种肝功能得以保留。所有结果表明,PHBV微球是肝组织工程的合适支架。