Jiang D, Xie Q, Li M
Department of Blood Physiology, Hunan Medical University, Changsha.
Hunan Yi Ke Da Xue Xue Bao. 1997;22(2):99-101.
The effects of media buffered with HEPES of different concentrations and different incubation periods on the proliferation and differentiation of CFU-GM were studied under the standard condition for culture. The results exhibited that when the incubation period prolonged, the pH values of culture system raised and the colony formation of CFU-GM decreased; the culture system added with proper HEPES buffer solution could maintain and increase the colony formation of CFU-GM, especially the culture system in which the pH value was not adjusted before the experiment. We also found that media buffered with HEPES could change the ratio of different colony types. This showed that media buffered with HEPES could not only stimulate the proliferation of CFU-GM, but also affect its differentiation. The results suggest that media buffered with HEPES are better than those without HEPES for the culture of hematopoietic progenitor cells, and the optimum concentration is 10-20 mmol.L-1.
在标准培养条件下,研究了不同浓度HEPES缓冲的培养基以及不同培养时间对CFU-GM增殖和分化的影响。结果显示,随着培养时间延长,培养体系的pH值升高,CFU-GM的集落形成减少;添加适当HEPES缓冲溶液的培养体系可维持并增加CFU-GM的集落形成,尤其是实验前未调节pH值的培养体系。我们还发现,HEPES缓冲的培养基可改变不同集落类型的比例。这表明,HEPES缓冲的培养基不仅能刺激CFU-GM的增殖,还能影响其分化。结果表明,对于造血祖细胞培养,HEPES缓冲的培养基优于未添加HEPES的培养基,最佳浓度为10 - 20 mmol·L-1。