Zarling J M, Shoyab M, Marquardt H, Hanson M B, Lioubin M N, Todaro G J
Proc Natl Acad Sci U S A. 1986 Dec;83(24):9739-43. doi: 10.1073/pnas.83.24.9739.
A polypeptide termed oncostatin M, which inhibits the replication of A375 melanoma and other human tumor cells, but not normal human fibroblasts, has been isolated from serum-free supernatants of U-937 histiocytic lymphoma cells that have been induced to differentiate into macrophage-like cells following treatment with the phorbol ester phorbol 12-myristate 13-acetate. No such growth inhibitory activity is detected in the supernatant of untreated U-937 cells, indicating that the protein is induced or increased in expression in the phorbol ester-induced differentiated cells. Oncostatin M is stable between pH 2 and 11 and after heating for 1 hr at 56 degrees C but is not stable at 90 degrees C. Purification of oncostatin M has been achieved by gel chromatography and reversed-phase HPLC, using sequentially acetonitrile and n-propanol in the presence of aqueous trifluoroacetic acid. The apparent molecular weight of oncostatin M is approximately 18,000, as determined by gel chromatography, and 28,000, as determined by polyacrylamide gel electrophoresis. The amino-terminal amino acid sequence of the purified polypeptide has been determined. No substantial sequence homology between oncostatin M and other proteins was found, including other tumor cell inhibitory proteins produced by mononuclear cells. Oncostatin M, therefore, appears to represent a distinct cell growth regulator.
一种名为制瘤素M的多肽已从U - 937组织细胞淋巴瘤细胞的无血清上清液中分离出来。该细胞在用佛波酯佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯处理后被诱导分化为巨噬细胞样细胞,制瘤素M可抑制A375黑色素瘤和其他人类肿瘤细胞的复制,但不抑制正常人类成纤维细胞。在未处理的U - 937细胞的上清液中未检测到这种生长抑制活性,这表明该蛋白在佛波酯诱导的分化细胞中被诱导或表达增加。制瘤素M在pH 2至11之间以及在56℃加热1小时后是稳定的,但在90℃时不稳定。通过凝胶色谱和反相高效液相色谱法实现了制瘤素M的纯化,在三氟乙酸水溶液存在下依次使用乙腈和正丙醇。通过凝胶色谱法测定,制瘤素M的表观分子量约为18,000,通过聚丙烯酰胺凝胶电泳测定为28,000。已确定纯化多肽的氨基末端氨基酸序列。未发现制瘤素M与其他蛋白质之间存在实质性的序列同源性,包括单核细胞产生的其他肿瘤细胞抑制蛋白。因此,制瘤素M似乎代表一种独特的细胞生长调节因子。