Su B, Zhang S, Yu W
Burn Institute, Changhai Hospital, Second Military Medical University.
Zhonghua Zheng Xing Shao Shang Wai Ke Za Zhi. 1995 Nov;11(6):433-5.
We propose a modification of the conventional keratinocyte subculture method, showing a significant improvement in the colony growth capacity of subcultured keratinocytes. This method utilized mouse 3T3 fibroblasts and MCDB153 medium, and it has been shown that they could improve the colony growth of human keratinocytes. Compare with the conventional procedure, this culture method was shorter in time, and resulted in a higher colony growth capacity of cells, reaching confluence 3 days earlier. In the treatment of extensively burned patients using cultured epidermal sheets, the time required for their production remains the main problem. Thus, the significantly reduced time to obtain confluent keratinocyte sheets with our method is very important for the treatment of large burn wounds.
我们提出了一种对传统角质形成细胞传代培养方法的改进方法,该方法显示出传代培养的角质形成细胞集落生长能力有显著提高。此方法使用小鼠3T3成纤维细胞和MCDB153培养基,并且已表明它们可改善人角质形成细胞的集落生长。与传统方法相比,这种培养方法所需时间更短,细胞的集落生长能力更高,提前3天达到汇合状态。在使用培养的表皮片治疗大面积烧伤患者时,生产所需时间仍然是主要问题。因此,用我们的方法获得汇合角质形成细胞片的时间显著缩短,这对于治疗大面积烧伤创面非常重要。