Riss T L, Sirbasku D A
Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston 77225.
In Vitro Cell Dev Biol. 1987 Dec;23(12):841-9. doi: 10.1007/BF02620963.
Transferrin was identified as a major tissue-derived growth factor for MTW9/PL2 rat mammary tumor cells. Mitogenic activity was assayed by the ability to stimulate the increase in number of MTW9/PL2 cells over 4 d in Dulbecco's modified Eagle's medium containing only 15 mM HEPES, 2 mM glutamine, and 50 micrograms/ml gentamicin. This growth-promoting activity was purified from ammonium sulfate precipitates of phosphate buffered saline extracts of porcine pituitaries using DEAE-Sepharose, chromatofocusing, molecular sieve chromatography and reverse phase high performance liquid chromatography. Pig pituitary mitogen (PPM) migrated as a single band at molecular weight 78,000 on sodium dodecyl sulfate polyacrylamide gel electrophoresis, eluted from chromatofocusing at multiple pH values near 6.3, exhibited an absorption maximum at 465 nm which was diminished by removal of iron, showed a characteristic salmon-pink color in aqueous solution, and was similar in amino acid composition to previously reported values for porcine transferrin. Purified PPM stimulated the growth of MTW9/PL2 cells with mitogenic potency (ED50 = 190 to 280 ng/ml) similar to commercially available human transferrin (ED50 = 160 to 350 ng/ml). We have concluded that using serum-free assay conditions with MTW9/PL2 cells, transferrin was a major source of the mitogenic activity present in extracts of porcine pituitary.
转铁蛋白被鉴定为MTW9/PL2大鼠乳腺肿瘤细胞的一种主要的组织来源生长因子。通过在仅含有15 mM HEPES、2 mM谷氨酰胺和50微克/毫升庆大霉素的杜尔贝科改良伊格尔培养基中刺激MTW9/PL2细胞在4天内数量增加的能力来测定促有丝分裂活性。这种促生长活性是从猪垂体的磷酸盐缓冲盐水提取物的硫酸铵沉淀中纯化得到的,使用了DEAE-琼脂糖、色谱聚焦、分子筛色谱和反相高效液相色谱。猪垂体促有丝分裂原(PPM)在十二烷基硫酸钠聚丙烯酰胺凝胶电泳上以分子量78,000迁移为单一条带,在接近6.3的多个pH值下从色谱聚焦中洗脱,在465 nm处有最大吸收,去除铁后吸收减弱,在水溶液中呈现特征性的鲑鱼粉红色,并且氨基酸组成与先前报道的猪转铁蛋白值相似。纯化的PPM刺激MTW9/PL2细胞生长,其促有丝分裂效力(ED50 = 190至280 ng/ml)与市售人转铁蛋白(ED50 = 160至350 ng/ml)相似。我们得出结论,在使用MTW9/PL2细胞的无血清测定条件下,转铁蛋白是猪垂体提取物中促有丝分裂活性的主要来源。