Sakai N, Tsuneoka K, Shikita M
J Cell Physiol. 1984 Jan;118(1):1-5. doi: 10.1002/jcp.1041180102.
Continuous ambulatory peritoneal dialysis (CAPD) fluid from three patients with chronic renal failure exhibited the activity of colony-stimulating factor (CSF) in amounts varying from 5 to 40 units per ml. Like the CSF obtained from normal human urine, the peritoneal CSF predominantly produced monocyte/macrophage colonies in soft-agar culture of mouse bone marrow cells. Semipurified peritoneal CSF showed its isoelectric point at pH 3.6 and 4.9 before and after the treatment with neuraminidase. Under the same conditions, the urinary CSF was focused at pH 3.1 and 4.6. The position of elution of the peritoneal and urinary CSF in ordinary gel-filtration chromatography corresponded to a molecular weight of 62,000 and 117,000, whereas both CSFs exhibited a molecular weight of 28,000 upon gel-filtration in the presence of 6 M guanidine HCl. Furthermore, the two CSFs from the human sources were neutralized by antimouse L cell CSF serum in the same manner. We conclude that the peritoneal CSF is a sialoglycoprotein which is nearly identical with the urinary CSF despite processing of the latter through kidneys.
三名慢性肾功能衰竭患者的持续性非卧床腹膜透析(CAPD)液呈现出集落刺激因子(CSF)活性,其含量在每毫升5至40单位之间变化。与从正常人尿液中获得的CSF一样,腹膜CSF在小鼠骨髓细胞的软琼脂培养中主要产生单核细胞/巨噬细胞集落。经神经氨酸酶处理前后,半纯化的腹膜CSF在pH 3.6和4.9处显示其等电点。在相同条件下,尿液CSF聚焦于pH 3.1和4.6。在普通凝胶过滤色谱中,腹膜CSF和尿液CSF的洗脱位置对应于分子量62,000和117,000,而在6 M盐酸胍存在下进行凝胶过滤时,两种CSF均呈现分子量28,000。此外,来自人类来源的两种CSF以相同方式被抗小鼠L细胞CSF血清中和。我们得出结论,腹膜CSF是一种唾液糖蛋白,尽管尿液CSF经过肾脏处理,但它与尿液CSF几乎相同。