Stam K, Stewart A A, Qu G Y, Iwata K K, Fenyö D, Chait B T, Marshak D R, Haley J D
Pharmaceuticals Division, Oncogene Science, Uniondale, NY 11553.
Biochem J. 1995 Jan 1;305 ( Pt 1)(Pt 1):87-92. doi: 10.1042/bj3050087.
Epithelial- and haematopoietic-cell growth-inhibitory activities have been identified in the conditioned medium of the human peripheral neuroepithelioma cell line A673. An A673-cell-derived growth-inhibitory activity was previously fractionated into two distinct components which inhibited the proliferation of human carcinoma and leukaemia cells in culture. One inhibitory activity was shown to comprise interleukin-1 alpha (IL-1 alpha). Here, we have purified to homogeneity a distinct activity which inhibited the growth of the epithelial cells in vitro. Using a combination of protein-sequence analysis and mass spectrometry, we demonstrated that biological activity can be assigned to a dimeric protein with a molecular mass of 25,576 (+/- 4) Da and an N-terminal sequence identical with that of transforming growth factor-beta 1 (TGF-beta 1). Further characterization of the growth inhibitor with TGF-beta-isoform-specific antibodies showed that > 90% of the bioactivity consists of TGF-beta 1 and not TGF-beta 2 or TGF-beta 3. Although A673 cells were growth-inhibited by exogenous TGF-beta 1, we showed that TGF-beta 1 in A673-cell-conditioned media was present in the latent, biologically inactive, form which did not act as an autocrine growth modulator of A673 cells in vitro.
在人外周神经上皮瘤细胞系A673的条件培养基中已鉴定出上皮细胞和造血细胞生长抑制活性。先前将A673细胞衍生的生长抑制活性分离为两个不同的组分,它们在培养中抑制人癌细胞和白血病细胞的增殖。其中一种抑制活性被证明包含白细胞介素-1α(IL-1α)。在此,我们已将一种能在体外抑制上皮细胞生长的独特活性纯化至同质状态。通过结合蛋白质序列分析和质谱分析,我们证明该生物活性可归因于一种分子量为25,576(±4)Da的二聚体蛋白,其N端序列与转化生长因子-β1(TGF-β1)相同。用TGF-β同工型特异性抗体对该生长抑制剂进行的进一步表征表明,>90%的生物活性由TGF-β1组成,而非TGF-β2或TGF-β3。尽管外源性TGF-β1可抑制A673细胞生长,但我们发现A673细胞条件培养基中的TGF-β1以潜伏的、无生物活性的形式存在,在体外它不作为A673细胞的自分泌生长调节剂。