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首页> 外文期刊>Journal of cell biology >Role of serum components in density-dependent inhibition of growth of cells in culture. Platelet-derived growth factor is the major serum determinant of saturation density
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Role of serum components in density-dependent inhibition of growth of cells in culture. Platelet-derived growth factor is the major serum determinant of saturation density

机译:血清成分在密度依赖性抑制培养细胞生长中的作用。血小板衍生的生长因子是饱和度密度的主要血清决定因素

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The effects of platelet-derived growth factor and plasma components on saturation density in cultures of 3T3 cells were investigated. Both of these components of whole blood serum affect saturation density; however, when 3T3 cells become quiescent at high density in medium containing whole blood serum, only platelet-derived growth factor and fresh whole blood serum are capable of stimulating proliferation. Addition of fresh plasma- derived serum has little effect on cell growth. These results suggest that the platelet factor is the major determinant of saturation density in cultures of 3T3 cells maintained in medium supplemented with whole blood serum.Experiments were performed to investigate the mechanism by which platelet-derived growth factor regulates saturation density. We investigated the possibilities of inactivation of growth factors by proliferating cells, and the effects of cell density on the response of 3T3 cells to platelet-derived growth factor. The amount of platelet- derived growth factor required to initiated DNA synthesis increases with increasing cell density. Some inactivation of growth factors by growing cells was detected, but this depletion was only evident at high cell density. We propose that density-dependent inhibition in cultured 3T3 cells is the result both of an increased requirement for the platelet- derived growth factor as the cultures become more crowded and of inactivation of growth factor activity by growing cells.
机译:研究了血小板衍生的生长因子和血浆成分对3T3细胞培养物中饱和密度的影响。全血清的这两个成分都会影响饱和度密度。然而,当3T3细胞在含有全血清的培养基中以高密度静止时,只有血小板衍生的生长因子和新鲜的全血清能够刺激增殖。添加新鲜血浆来源的血清对细胞生长影响很小。这些结果表明,血小板因子是在补充全血清的培养基中维持的3T3细胞培养物中饱和密度的主要决定因素。进行了实验以研究血小板衍生的生长因子调节饱和密度的机制。我们研究了通过增殖细胞使生长因子失活的可能性,以及细胞密度对3T3细胞对血小板衍生生长因子的反应的影响。启动DNA合成所需的血小板衍生生长因子的数量随细胞密度的增加而增加。检测到通过生长的细胞使生长因子失活,但是这种消耗仅在高细胞密度时才明显。我们提出,在培养的3T3细胞中密度依赖性抑制是由于随着培养物变得更加拥挤而对血小板衍生生长因子的需求增加以及生长细胞使生长因子活性失活的结果。

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