Rosen E M, Joseph A, Jin L, Rockwell S, Elias J A, Knesel J, Wines J, McClellan J, Kluger M J, Goldberg I D
Department of Radiation Oncology, Long Island Jewish Medical Center, New Hyde Park, New York 11042.
J Cell Biol. 1994 Oct;127(1):225-34. doi: 10.1083/jcb.127.1.225.
Scatter factor (SF) (also known as hepatocyte growth factor [HGF]) is a fibroblast-derived cytokine that stimulates motility, proliferation, and morphogenesis of epithelia. SF may play major roles in development, repair, and carcinogenesis. However, the physiologic signals that regulate its production are not well delineated. We found that various human tumor cell lines that do not produce SF secrete factors that stimulate SF production by fibroblasts, suggesting a paracrine mechanism for regulation of SF production. Conditioned medium from these cell lines contained two distinct scatter factor-inducing factor SF-IF activities: a high molecular weight (> 30 kD), heat sensitive activity and a low molecular weight (< 30 kD) heat stable activity. Further studies revealed that SF-producing fibroblasts also secrete factors that stimulate their own SF production. We characterized the < 30-kD SF-IF activity from ras-3T3 (clone D4), a mouse cell line that overproduces both SF and SF-IF. The < 30-kD filtrate from ras-3T3 conditioned medium induced four- to sixfold increases in expression of SF biologic activity, immunoreactive protein, and mRNA by multiple SF-producing fibroblast lines. Ras-3T3 SF-IF activity was stable to boiling, extremes of pH, and reductive alkylation, but was destroyed by proteases. We purified ras-3T3 SF-IF about 10,000-fold from serum-free conditioned medium by a combination of ultrafiltration, cation exchange chromatography, and reverse phase chromatography. The purified protein exhibited electrophoretic mobility of about 12 kD (reduced) and 14 kD (nonreduced) by SDS-PAGE. The identity of the protein was verified by elution of biologic activity from gel slices. Purified SF-IF stimulated SF production in a physiologic concentration range (about 20-400 pM). Its properties and activities were distinct from those of IL-1 and TNF, two known inducers of SF production. We suggest that SF-IF is a physiologic regulator of SF production.
散射因子(SF)(也称为肝细胞生长因子 [HGF])是一种由成纤维细胞产生的细胞因子,可刺激上皮细胞的运动、增殖和形态发生。SF 可能在发育、修复和致癌过程中发挥主要作用。然而,调节其产生的生理信号尚未完全明确。我们发现,各种不产生 SF 的人类肿瘤细胞系会分泌刺激成纤维细胞产生 SF 的因子,提示存在一种旁分泌机制来调节 SF 的产生。这些细胞系的条件培养基含有两种不同的散射因子诱导因子 SF-IF 活性:一种高分子量(> 30 kD)、热敏感活性和一种低分子量(< 30 kD)热稳定活性。进一步研究表明,产生 SF 的成纤维细胞也会分泌刺激自身 SF 产生的因子。我们对来自 ras-3T3(克隆 D4)的 < 30-kD SF-IF 活性进行了表征,ras-3T3 是一种同时过量产生 SF 和 SF-IF 的小鼠细胞系。来自 ras-3T3 条件培养基的 < 30-kD 滤液使多种产生 SF 的成纤维细胞系的 SF 生物活性、免疫反应性蛋白和 mRNA 表达增加了四至六倍。Ras-3T3 SF-IF 活性对煮沸、极端 pH 值和还原烷基化稳定,但被蛋白酶破坏。我们通过超滤、阳离子交换色谱和反相色谱相结合的方法,从无血清条件培养基中纯化了 ras-3T3 SF-IF 约 10,000 倍。通过 SDS-PAGE 分析,纯化后的蛋白质在还原条件下的电泳迁移率约为 12 kD,非还原条件下约为 14 kD。通过从凝胶切片中洗脱生物活性验证了该蛋白质的身份。纯化的 SF-IF 在生理浓度范围(约 20 - 400 pM)内刺激 SF 的产生。其性质和活性与已知的两种 SF 产生诱导因子 IL-1 和 TNF 不同。我们认为 SF-IF 是 SF 产生的生理调节因子。