人癌细胞系RPMI 2650产生的自刺激生长因子。

B M Carey, M Dooley, R Weedle, M Clynes
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引用次数: 2

摘要

人癌细胞RPMI 2650产生自分泌因子;通过RPMI 2650条件培养基(CM)刺激低密度RPMI 2650细胞在软琼脂中生长的能力来检测它们。粗CM中的自分泌活性可通过超滤分离成较低分子量(MW)的馏分(R1-30),其分子集中在1000- 30000 Da范围内;分子量更高的分数(R30),分子大于30,000 Da,以更浓缩的形式存在。R1-30对酸、碱和热处理不稳定,而R30对这些处理是稳定的(有时被这些处理激活)。然而,R30的煮沸使其对酸、碱和胰蛋白酶的处理不稳定。CM可分为弱肝素结合部分(稳定性与R1-30相似,但不完全相同)和非肝素结合部分(稳定性与R30相似)。RPMI 2650细胞分泌转化生长因子(TGF) α -和TGF β样分子,但R1-30部分可以通过其不同寻常的酸不稳定性和对肝素的弱亲和力与这些TGF -和大多数其他已知的生长因子区分开来。由于R30/非肝素结合部分通过煮沸或酸处理变得不稳定,它可能代表一种结合或构象稳定的生长因子形式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production of autostimulatory growth factors by the human carcinoma line, RPMI 2650.

The human carcinoma line RPMI 2650 produces autocrine factors; they are detected by the ability of RPMI 2650 conditioned medium (CM) to stimulate growth in soft agar of RPMI 2650 cells plated at low density. The autocrine activity in crude CM can be fractionated by ultrafiltration into a lower molecular weight (MW) fraction (R1-30), which concentrates molecules in the 1000-30,000 Da range; and a higher MW fraction (R30) with molecules greater than 30,000 Da in a more concentrated form. R1-30 is labile to acid, base, and heat treatment, whereas R30 is stable to (and sometimes activated by) these treatments. Boiling of R30, however, renders it labile to acid, base, and trypsin treatments. CM can be separated into a weakly heparin-binding fraction (with stability properties similar, but not identical, to R1-30), and a non-heparin binding fraction (with stability properties similar to R30). RPMI 2650 cells secrete transforming growth factor (TGF)alpha- and TGF beta-like molecules, but the R1-30 fraction can be distinguished from these TGFs, and from most other known growth factors, by its unusual combination of acid lability and weak affinity for heparin. Since the R30/non-heparin binding fraction is rendered labile by boiling or acid treatment, it may represent a bound or conformationally stable form of a growth factor.

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