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猿猴病毒40转化的3T3细胞对生长因子依赖性降低的分析。

Analysis of the reduced growth factor dependency of simian virus 40-transformed 3T3 cells.

作者信息

Powers S, Fisher P B, Pollack R

出版信息

Mol Cell Biol. 1984 Aug;4(8):1572-6. doi: 10.1128/mcb.4.8.1572-1576.1984.

Abstract

We have measured in a defined serum-free medium the platelet-derived growth factor (PDGF) and insulin requirements of normal Swiss 3T3 cells, simian virus 40-transformed 3T3 cells, and partial revertants of simian virus 40-transformed 3T3 cells. Swiss 3T3 cells displayed strong requirements for both PDGF and insulin. Both of these requirements were significantly diminished in simian virus 40-transformed 3T3 cells. Analysis of the PDGF and insulin requirements of the revertants indicated that the loss of either of these two growth factor requirements was not necessarily linked to the other; rather, the growth factor requirements were specifically associated with other parameters of transformation. The reacquisition of a PDGF requirement cosegregated with reversion to density-dependent growth inhibition, whereas reacquisition of a normal insulin requirement cosegregated with reversion to a normal growth dependence on calf serum. Anchorage dependence was dissociable from both growth factor requirements. The relationship between the PDGF requirement and density-dependent growth inhibition was further analyzed in normal 3T3 cells by measuring the PDGF requirement at different cell densities. At high cell densities, the requirement for PDGF became significantly greater. We suggest that at least in part the ability of transformed cells to grow to high saturation densities results from their loss of a requirement for PDGF.

摘要

我们在一种特定的无血清培养基中测定了正常瑞士3T3细胞、猿猴病毒40转化的3T3细胞以及猿猴病毒40转化的3T3细胞的部分回复突变体对血小板衍生生长因子(PDGF)和胰岛素的需求。瑞士3T3细胞对PDGF和胰岛素均有强烈需求。在猿猴病毒40转化的3T3细胞中,这两种需求均显著降低。对回复突变体的PDGF和胰岛素需求分析表明,这两种生长因子需求中任何一种的丧失并不一定与另一种相关;相反,生长因子需求与其他转化参数有特定关联。对PDGF需求的重新获得与恢复密度依赖性生长抑制共分离,而正常胰岛素需求的重新获得与恢复对小牛血清的正常生长依赖性共分离。贴壁依赖性与两种生长因子需求均可分离。通过在不同细胞密度下测量PDGF需求,进一步分析了正常3T3细胞中PDGF需求与密度依赖性生长抑制之间的关系。在高细胞密度下,对PDGF的需求显著增加。我们认为,至少部分转化细胞生长至高饱和密度的能力源于它们对PDGF需求的丧失。

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