Chen Chun-Hung, Tsai Chen-Chi, Chen Wannhsin, Mi Fwu-Long, Liang Hsiang-Fa, Chen Sung-Ching, Sung Hsing-Wen
Department of Chemical Engineering, National Tsing Hua University, Hsinchu, Taiwan, ROC.
Biomacromolecules. 2006 Mar;7(3):736-43. doi: 10.1021/bm0506400.
In this study, a novel yet simple method, using a thermoreversible hydrogel system coated on tissue culture polystyrene (TCPS) dishes, was developed for harvesting living cell sheets. The hydrogel system was prepared by simply pouring aqueous methylcellulose (MC) solutions blended with distinct salts on TCPS dishes at 20 degrees C. For the applications to cell culture, only those aqueous MC compositions that may form a gel at 37 degrees C were chosen for the study. It was found that the hydrogel coating composed of 8% MC blended with 10 g/L PBS (phosphate buffered saline) (the MC/PBS hydrogel, with a gelation temperature of approximately 25 degrees C) stayed intact throughout the entire course of cell culture. To improve cell attachments, the MC/PBS hydrogel at 37 degrees C was evenly spread with a neutral aqueous collagen at 4 degrees C. The spread aqueous collagen gradually reconstituted with time and thus formed a thin layer of collagen (the MC/PBS/collagen hydrogel). After cells reached confluence, a continuous monolayer cell sheet formed on the surface of the MC/PBS/collagen hydrogel. When the grown cell sheet was placed outside of the incubator at 20 degrees C, it detached gradually from the surface of the thermoreversible hydrogel spontaneously, without treating with any enzymes. The results obtained in the MTT assay demonstrated that the cells cultured on the surface of the MC/PBS/collagen hydrogel had an even better activity than those cultured on an uncoated TCPS dish. After harvesting the detached cell sheet, the remaining viscous hydrogel system is reusable. Additionally, the developed hydrogel system can be used for culturing a multilayer cell sheet. The obtained living cell sheets may be used for tissue reconstructions.
在本研究中,开发了一种新颖且简单的方法,即使用涂覆在组织培养聚苯乙烯(TCPS)培养皿上的热可逆水凝胶系统来收获活细胞片。通过在20℃下将与不同盐混合的甲基纤维素(MC)水溶液简单地倒在TCPS培养皿上来制备水凝胶系统。对于细胞培养应用,仅选择那些在37℃下可能形成凝胶的MC水溶液组合物进行研究。发现由8%MC与10 g/L PBS(磷酸盐缓冲盐水)混合组成的水凝胶涂层(MC/PBS水凝胶,凝胶化温度约为25℃)在细胞培养的整个过程中保持完整。为了改善细胞附着,在37℃下将MC/PBS水凝胶与4℃下的中性胶原水溶液均匀铺展。铺展的胶原水溶液随时间逐渐重构,从而形成一层薄的胶原层(MC/PBS/胶原水凝胶)。细胞达到汇合后,在MC/PBS/胶原水凝胶表面形成连续的单层细胞片。当生长的细胞片置于20℃的培养箱外时,它会自发地从热可逆水凝胶表面逐渐分离,无需用任何酶处理。MTT分析获得的结果表明,在MC/PBS/胶原水凝胶表面培养的细胞比在未涂覆的TCPS培养皿上培养的细胞具有更好的活性。收获分离的细胞片后,剩余的粘性水凝胶系统可重复使用。此外,所开发的水凝胶系统可用于培养多层细胞片。获得的活细胞片可用于组织重建。