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生长因子在形态学上对佛波酯(TPA)耐药的Balb/c3T3 TR4细胞中诱导膜皱褶形成。

Induction of membrane ruffling by growth factors in morphologically TPA-resistant Balb/c3T3 TR4 cells.

作者信息

Enomoto T, Asano Y

机构信息

Department of Radiation Biophysics and genetics, Kobe University School of Medicine, Japan.

出版信息

Cell Struct Funct. 1994 Apr;19(2):89-96. doi: 10.1247/csf.19.89.

Abstract

To investigate the biological characteristics of a Balb/c3T3 variant TR4 clone which is morphologically resistant to TPA and hypersensitive to v-src induced metastasis, we compared the responsiveness of the variant and its parent cells to growth factor-induced membrane ruffling. When the confluent cells were stimulated with PDGF, membrane ruffling was rapidly induced in TR4 but not in the parent cell cultures. In TR4 cells, membrane ruffling was observed under a phase-contrast microscope within 2 min after the addition of PDGF, reaching the maximum 5 min later and thereafter decreased gradually to the control level. There were no apparent differences in 125I-PDGF binding kinetics between TR4 and parent cells. Similar membrane ruffling was induced by other growth factors such as insulin, IGF-I, acidic or basic FGF but not by EGF or alpha- and beta-TGF, only in TR4 cells. When TR4 cells were incubated with TPA just before stimulation with these growth factors, growth factor-induced membrane ruffling was completely inhibited. Also, 5 out of 6 clones of stable fusion cells between TR4 and parent cells showed the parental type of responses to TPA and growth factors, indicating that the TR4 phenotype is recessive. These results suggest that the variant TR4 cells may acquire the genetic and recessive alteration of a cellular factor which is responsible for the regulation of growth factor-mediated membrane ruffling and that this genetic alteration occurs at a common step downstream of growth factor-mediated cascades, rather than at their receptor level.

摘要

为了研究对佛波酯(TPA)具有形态学抗性且对v-src诱导的转移高度敏感的Balb/c3T3变异体TR4克隆的生物学特性,我们比较了该变异体及其亲本细胞对生长因子诱导的膜皱襞形成的反应性。当用血小板衍生生长因子(PDGF)刺激汇合细胞时,TR4细胞中迅速诱导出膜皱襞形成,而亲本细胞培养物中则未出现。在TR4细胞中,添加PDGF后2分钟内在相差显微镜下即可观察到膜皱襞形成,5分钟后达到最大值,此后逐渐降至对照水平。TR4细胞与亲本细胞之间的125I-PDGF结合动力学没有明显差异。仅在TR4细胞中,胰岛素、胰岛素样生长因子-I(IGF-I)、酸性或碱性成纤维细胞生长因子(FGF)等其他生长因子可诱导类似的膜皱襞形成,而表皮生长因子(EGF)或α和β转化生长因子(TGF)则不能。当在这些生长因子刺激前将TR4细胞与TPA一起孵育时,生长因子诱导的膜皱襞形成被完全抑制。此外,TR4细胞与亲本细胞之间的6个稳定融合细胞克隆中有5个对TPA和生长因子表现出亲本类型的反应,表明TR4表型是隐性的。这些结果表明,变异体TR4细胞可能获得了一种细胞因子的遗传和隐性改变,该细胞因子负责调节生长因子介导的膜皱襞形成,并且这种遗传改变发生在生长因子介导的级联反应的共同下游步骤,而不是在其受体水平。

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