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在SV40转化的3T3成纤维细胞的无血清条件培养基中存在转化生长因子的证据。

Evidence for a transforming growth factor(s) in the serum-free conditioned medium of SV40-transformed 3T3 fibroblasts.

作者信息

Pirozzi S, Young D V

出版信息

Int J Cancer. 1984 Apr 15;33(4):525-32. doi: 10.1002/ijc.2910330417.

Abstract

Unlike untransformed 3T3 fibroblasts, Simian Virus 40-transformed 3T3 cells (SV3T3) do not require the presence of exogenous polypeptide mitogens in order to become competent for the initiation of DNA synthesis. As an explanation for this state of perpetual competence, growth activity for 3T3 cells was found in the serum-free conditioned medium of SV3T3 cells. This activity, which is abolished by incubation with pepsin, but withstands to a fair degree denaturants (8 M urea and 4 M guanidinium HCl) and a reducing agent (65 mM dithioerythritol), enhances the growth of Swiss and BALB/c 3T3 cells in 1% (v/v) calf serum medium and ensures the complete survival of Swiss 3T3 cells for several days in the total absence of serum. The growth activity appears to be derived from the SV3T3 cells, since it is not found in the non-conditioned medium (and the insulin and transferrin components of this serum-free medium have only weak growth activity alone) and the chances of it being due to residual serum growth factors are slight because of the method of growing the cells and the collection of the conditioned medium. Moreover, in a separate experiment to test the possible involvement of cell attachment factors, rat fibronectin was found not to affect 3T3 growth in the standard growth assay. The conditioned medium growth activity apparently has the biological capabilities of transforming growth factors. After concentration by ammonium sulfate precipitation, it can stimulate DNA synthesis in confluent, quiescent Swiss 3T3 cells, in both the absence and presence of 10% depleted calf serum. It also permits the growth of large colonies of Swiss 3T3 cells in soft agar. As part of a preliminary characterization of the conditioned medium growth activity, gel filtration in 0.15 M NaCl, 0.001 M HCl resolves the activity into high (mol. wt. greater than or equal to 100,000) and low (mol. wt. 5,000-6,000) molecular weight factors. Since re-chromatography of the high molecular weight factor, which may still be in an aggregated form, does not generate the smaller, the latter is not a dissociation product of the former. The precise relationship of these SV3T3-conditioned medium growth factors to other growth factors, including known transforming growth factors, has not yet been determined.

摘要

与未转化的3T3成纤维细胞不同,猿猴病毒40转化的3T3细胞(SV3T3)在启动DNA合成时无需外源性多肽促有丝分裂原的存在。作为对这种持续感受态状态的一种解释,在SV3T3细胞的无血清条件培养基中发现了对3T3细胞的生长活性。这种活性在用胃蛋白酶孵育后会被消除,但在相当程度上能耐受变性剂(8M尿素和4M盐酸胍)和还原剂(65mM二硫赤藓糖醇),它能增强瑞士和BALB/c 3T3细胞在1%(v/v)小牛血清培养基中的生长,并确保瑞士3T3细胞在完全无血清的情况下存活数天。这种生长活性似乎源自SV3T3细胞,因为在未条件培养基中未发现它(并且这种无血清培养基中的胰岛素和转铁蛋白成分单独只有微弱的生长活性),而且由于细胞培养方法和条件培养基的收集方式,其由残留血清生长因子导致的可能性很小。此外,在另一个测试细胞附着因子可能参与情况的实验中,发现大鼠纤连蛋白在标准生长试验中不影响3T3细胞的生长。条件培养基生长活性显然具有转化生长因子的生物学能力。经硫酸铵沉淀浓缩后,它能在汇合的、静止的瑞士3T3细胞中刺激DNA合成,无论有无10%的耗尽小牛血清。它还能使瑞士3T3细胞在软琼脂中形成大菌落生长。作为对条件培养基生长活性初步表征的一部分,在0.15M NaCl、0.001M HCl中进行凝胶过滤将该活性分离为高分子量(分子量大于或等于100,000)和低分子量(分子量5,000 - 6,000)因子。由于可能仍呈聚集形式的高分子量因子重新层析后不会产生较小的因子,所以后者不是前者的解离产物。这些SV3T3条件培养基生长因子与其他生长因子(包括已知的转化生长因子)的确切关系尚未确定。

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