Jaumotte-Thelen S, Dozet-Dupont I, Marchand-Brynaert J, Schneider Y J
Laboratoire de Biochimie cellulaire, Université catholique de Louvain, Louvain-la-Neuve, Belgium.
J Biomed Mater Res. 1996 Dec;32(4):569-82. doi: 10.1002/(SICI)1097-4636(199612)32:4<569::AID-JBM10>3.0.CO;2-9.
The adhesion and differentiation of rat hepatocytes onto track-etched poly(ethylene terephthalate) (PET) membranes were studied. Native or [3H]methylated fibronectin (FN) or asialofetuin (ASF) were immobilized onto oxidized PET membranes, preactivated or not with carbodiimide (WSC). Radiochemical assay and ELISA indicated that upon washing in SDS or in serum-containing medium, significantly less FN was released from WSC-activated membranes that from unactivated ones. These differences were abolished when the NH2 functions of FN were fully acetylated, suggesting that part of FN was covalently grafted on WSC-activated PET. Although weaker, a comparable effect was observed with ASF. Hepatocytes adhered faster on membranes on which FN was grafted than adsorbed, reaching values comparable to collagen-coated PET; after 24 h these differences decreased. Experiments with cycloheximide or at 4 degrees C suggested that this results from secretion of extracellular matrix adsorbing on PET. Phase I or II biotransformation activities of cells cultured for 1-4 days on FN-, ASF-, or collagen-treated substrates were not significantly different. These results indicate that stable immobilization of FN (covalent grafting) onto PET membranes significantly accelerates adhesion of hepatocytes but does not affect their differentiation. This may result from a progressive surface reconditioning by neosynthesized extracellular matrix.
研究了大鼠肝细胞在径迹蚀刻聚对苯二甲酸乙二酯(PET)膜上的黏附与分化情况。将天然或[³H]甲基化的纤连蛋白(FN)或去唾液酸胎球蛋白(ASF)固定在经或未经碳二亚胺(WSC)预活化的氧化PET膜上。放射化学分析和酶联免疫吸附测定表明,在SDS或含血清培养基中洗涤后,与未活化的膜相比,从WSC活化的膜上释放的FN显著减少。当FN的氨基功能完全乙酰化时,这些差异消失,这表明部分FN共价接枝到了WSC活化的PET上。虽然ASF的效果较弱,但也观察到了类似的作用。肝细胞在接枝有FN的膜上比在吸附有FN的膜上黏附得更快,达到了与胶原包被的PET相当的值;24小时后这些差异减小。用放线菌酮或在4℃下进行的实验表明,这是由于吸附在PET上的细胞外基质分泌所致。在FN、ASF或胶原处理的底物上培养1 - 4天的细胞的I相或II相生物转化活性没有显著差异。这些结果表明,将FN稳定固定(共价接枝)到PET膜上可显著加速肝细胞的黏附,但不影响其分化。这可能是由于新合成的细胞外基质对表面进行逐步修复的结果。