Koopman P, Cotton R G
Exp Cell Res. 1984 Sep;154(1):233-42. doi: 10.1016/0014-4827(84)90683-9.
Medium conditioned by STO mouse fibroblast cells inhibited both the spontaneous differentiation of NG2 embryonal carcinoma cells and the differentiation of F9 embryonal carcinoma cells induced by retinoic acid. This effect was due to a differentiation retarding factor (DRF). Reduction in DRF activity in conditioned medium by boiling and by pronase treatment suggested the involvement of a polypeptide, which had an apparent molecular weight of 57000 on gel filtration. A 28-fold purification of DRF was achieved. DRF delayed but did not prevent the extensive differentiation observed after prolonged culture of NG2 colonies. Conditioned medium could be successfully used to replace feeder cells in NG2 stock cultures. Media conditioned by a variety of other cell types also contained differentiation retarding activity.
由STO小鼠成纤维细胞条件化的培养基既能抑制NG2胚胎癌细胞的自发分化,也能抑制视黄酸诱导的F9胚胎癌细胞的分化。这种效应归因于一种分化抑制因子(DRF)。通过煮沸和链霉蛋白酶处理降低条件化培养基中DRF的活性,提示有一个多肽参与其中,该多肽在凝胶过滤中的表观分子量为57000。实现了DRF 28倍的纯化。DRF延迟但并未阻止NG2集落长期培养后观察到的广泛分化。条件化培养基可成功用于替代NG2原代培养中的饲养细胞。由多种其他细胞类型条件化的培养基也含有分化抑制活性。