Burgess A W, Metcalf D
Exp Hematol. 1977 Nov;5(6):456-64.
Granulocyte-macrophage colony stimulating factor (GM-CSF) from mouse lung conditioned medium has recently been purified. This GM-CSF was radioiodinated using the chloramine T method, but dimethylsulfoxide was needed to prevent the loss of biological activity during the iodination. 125I-labeled GM-CSF was isolated from the reaction mixture by gel filtration and affinity chromatography with concanavalin A-Sepharose. One hour after intravenous injection of 125I-labeled GM-CSF almost 80% of the radioactivity was still localized in the serum. 125I-labeled GM-CSF was cleared from the blood of C57BL mice with a serum half-life of 7.3 +/- 1.3 hours. Six hours after intravenous injection 125I-GM-CSF appeared to be distributed throughout most of the tissues of C57BL mice. There was no selective concentration of 125I-labeled GM-CSF in the bone marrow, but levels in the kidney were three times higher than expected from the distribution of 125I-labeled mouse serum albumin. 125I detected in the blood 6 hours after injection of 125I-labeled GM-CSF was precipitable with trichloroacetic acid and bound to concanavalin A-Sepharose. 125I detected in the urine was not macromolecular and appeared to result from the degradation of 125I-labeled GM-CSF.
最近已从小鼠肺条件培养基中纯化出粒细胞-巨噬细胞集落刺激因子(GM-CSF)。使用氯胺T法对这种GM-CSF进行放射性碘化,但在碘化过程中需要二甲基亚砜来防止生物活性丧失。通过凝胶过滤和伴刀豆球蛋白A-琼脂糖亲和色谱从反应混合物中分离出125I标记的GM-CSF。静脉注射125I标记的GM-CSF 1小时后,几乎80%的放射性仍存在于血清中。125I标记的GM-CSF从C57BL小鼠血液中清除,血清半衰期为7.3±1.3小时。静脉注射125I-GM-CSF 6小时后,它似乎分布在C57BL小鼠的大部分组织中。125I标记的GM-CSF在骨髓中没有选择性浓集,但肾脏中的水平比125I标记的小鼠血清白蛋白分布预期的高三倍。注射125I标记的GM-CSF 6小时后在血液中检测到的125I可被三氯乙酸沉淀,并与伴刀豆球蛋白A-琼脂糖结合。在尿液中检测到的125I不是大分子,似乎是125I标记的GM-CSF降解所致。