Wang Juan, Du Li Xin
College of Animal Science and technology, Shandong Agricultural University, Taian, 271018.
Shi Yan Sheng Wu Xue Bao. 2004 Jun;37(3):247-50.
Gonadal primordial germ cells (PGCs) were isolated from 4.5-7.5-day-old chicken embryos. Factors influencing isolation and cloning of chicken PGCs were analyzed in this study. The results attained were as follows: Chicken PGCs proliferated fast in presence of 10% FBS. At primary culture, PGCs were co-cultured with the gonadal stromal cells. For subculture the chicken PGCs were plated with mitotically inactive feeder layer cells. Further research found that the PMEF (primary mice embryonic fibroblast) feeder cells were the most suitable for the growth of PGCs. When the cell culture medium was supplemented with LIF, FGF, SCF and IGF-I, the chicken PGCs were in the best condition. The chicken PGCs were easier to clone when isolated from 5.5-day-old embryonic gonads. In addition, the proper digestion time was 40s when PGCs colonies were passaged.
从4.5至7.5日龄的鸡胚中分离出性腺原始生殖细胞(PGCs)。本研究分析了影响鸡PGCs分离和克隆的因素。获得的结果如下:鸡PGCs在10%胎牛血清(FBS)存在下增殖迅速。原代培养时,PGCs与性腺基质细胞共培养。传代培养时,将鸡PGCs接种于有丝分裂不活跃的饲养层细胞上。进一步研究发现,原代小鼠胚胎成纤维细胞(PMEF)饲养细胞最适合PGCs生长。当细胞培养基中添加白血病抑制因子(LIF)、成纤维细胞生长因子(FGF)、干细胞因子(SCF)和胰岛素样生长因子-I(IGF-I)时,鸡PGCs处于最佳状态。从5.5日龄胚胎性腺中分离的鸡PGCs更易于克隆。此外,PGCs集落传代时合适的消化时间为40秒。