Niho Y, Kimura N, Yamano Y, Yamamoto Y, Hirota Y, Ono J, Takaki R
Int J Cell Cloning. 1985 Jan;3(1):22-32. doi: 10.1002/stem.5530030105.
Erythroid-potentiating activity (EPA) was detected in culture medium conditioned by a human cancer cell line (KONT) that produces colony-stimulating activity (CSA), using erythroid colony formation in vitro. EPA in the medium conditioned by the KONT cells (KONT-CM) was markedly heat stable. After treating KONT-CM at 80 degrees C for 30 min, 30% EPA remained, while CSA was completely inactivated. Both EPA and CSA appeared in approximately the same fractions of the gel filtration, indicating a molecular weight of approximately 30,000 daltons. EPA bound partially to Concanavalin-A Sepharose, whereas CSA almost did not bind. Our results indicate that EPA can be separated from CSA based on heat stability and binding to Concanavalin-A Sepharose.
利用体外红系集落形成,在由产生集落刺激活性(CSA)的人癌细胞系(KONT)条件培养的培养基中检测到红系增强活性(EPA)。KONT细胞条件培养的培养基(KONT-CM)中的EPA具有显著的热稳定性。在80℃处理KONT-CM 30分钟后,仍保留30%的EPA,而CSA则完全失活。EPA和CSA在凝胶过滤中出现于大致相同的级分中,表明分子量约为30,000道尔顿。EPA部分结合伴刀豆球蛋白A琼脂糖,而CSA几乎不结合。我们的结果表明,基于热稳定性和与伴刀豆球蛋白A琼脂糖的结合,EPA可与CSA分离。