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来自培养的正常大鼠肾细胞系的粒细胞-巨噬细胞集落刺激因子

Granulocyte-macrophage colony-stimulating factor from cultured normal rat kidney cell line.

作者信息

Wu M C, Reuben P M

出版信息

Exp Hematol. 1984 May;12(4):267-76.

PMID:6201375
Abstract

Serum-free medium conditioned by the normal rat kidney (NRK) cell line contains colony-stimulating factors (CSF) that stimulate the in vitro formation of granulocyte and macrophage colonies from rat, mouse, and human marrow. There are two types of CSF: NRK-CSF I stimulates rat and mouse marrow, while NRK-CSF II stimulates the human marrow. The NRK-CSF I has been partially purified to a specific activity of 5 X 10(7) units/mg by employing methods such as preparative isoelectrofocusing, gel filtration chromatography, and preparative gel electrophoresis. It has an isoelectric point of 5.1 and an apparent molecular weight of 35,000 daltons as estimated by gel filtration. It is stable at 50 degrees C for 30 min and relatively resistant to papain, but highly sensitive to trypsin, chymotrypsin, and subtilisin. The secretion of CSF by NRK cells is inhibited by actinomycin D (0.5 micrograms/ml) and cycloheximide (0.5 micrograms/ml), but not by cytosine arabinoside (5 micrograms/ml). Although the CSF activity is inactivated by periodate oxidation (5 mM), thus suggesting its glycoprotein nature, treatment of the CSF with neuraminidase and other glycosidases has no effect on its activity. Anti-NRK-CSF I antibody inhibits the rat/mouse-active CSF from all rat sources, but has no effect on the human-active CSF. Comparative studies with CSF from media conditioned by the transformed cell line (442) and from rat lung and spleen have shown that CSF I from different rat sources share similar isoelectric points, molecular weights, and immunological properties.

摘要

由正常大鼠肾(NRK)细胞系条件培养的无血清培养基含有集落刺激因子(CSF),该因子能刺激大鼠、小鼠和人类骨髓在体外形成粒细胞和巨噬细胞集落。有两种类型的CSF:NRK-CSF I刺激大鼠和小鼠骨髓,而NRK-CSF II刺激人类骨髓。通过制备性等电聚焦、凝胶过滤色谱和制备性凝胶电泳等方法,NRK-CSF I已被部分纯化至比活性为5×10⁷单位/毫克。通过凝胶过滤估计,其等电点为5.1,表观分子量为35,000道尔顿。它在50℃下稳定30分钟,对木瓜蛋白酶相对耐受,但对胰蛋白酶、胰凝乳蛋白酶和枯草杆菌蛋白酶高度敏感。NRK细胞分泌CSF受到放线菌素D(0.5微克/毫升)和环己酰亚胺(0.5微克/毫升)的抑制,但不受阿糖胞苷(5微克/毫升)的抑制。尽管CSF活性可被高碘酸盐氧化(5毫摩尔)灭活,从而提示其糖蛋白性质,但用神经氨酸酶和其他糖苷酶处理CSF对其活性没有影响。抗NRK-CSF I抗体抑制来自所有大鼠来源的大鼠/小鼠活性CSF,但对人类活性CSF没有影响。与来自转化细胞系(442)以及大鼠肺和脾条件培养的培养基中的CSF进行的比较研究表明,来自不同大鼠来源的CSF I具有相似的等电点、分子量和免疫特性。

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