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血清或焦磷酸钙复合物对Balb/c3T3细胞存活和增殖的协同控制

Coordinate control of Balb/c3T3 cell survival and multiplication by serum or calcium pyrophosphate complexes.

作者信息

Rubin A H, Bowen-Pope D F

出版信息

J Cell Physiol. 1979 Jan;98(1):81-94. doi: 10.1002/jcp.1040980110.

Abstract

Balb/c3T3 cells in crowded cultures detach from the dish when deprived of serum, and the survivors incorporate 3H-thymidine at a reduced rate. The detachment becomes pronounced two hours after removal of serum, and reaches its maximum rate between two and four hours. Cells in sparse culture are not detached by serum removal, and their rate of 3H-thymidine incorporation is only slightly reduced. As the sparse cultures grow into more crowded cultures, and the serum is depleted, increasing numbers detach. The detached cells are incapable of reattaching when placed in a new dish with ample fresh serum. The cells are leaky to cellular constituents and appear to be dead. Detachment is a consequence rather than the cause of cell death, and can be produced by agents which inhibit cellular energy metabolism. The cells on the dish which survive serum deprivation are fully viable and grow rapidly when serum is added. When they become crowded they are as sensitive to serum deprivation as was the original population. They are therefore not selected for a low serum requirement but apparently survive because they spread into the space vacated by the detaching cells and then behave as sparse cultures in response to serum variations. Insoluble complexes of Ca2+ and pyrophosphate (Ca2+-PPi) show the same concentration dependence in promoting cell survival as in stimulating 3H-thymidine incorporation, showing that a single substance can be responsible for both activities. It is concluded that survival and growth are part of the coordinate response of 3T3 cells to single external effectors. The results are discussed in terms of a simple model in which the coordinate response is regulated by the availability of Mg2+ for transphosphorylation reactions within the cell, and the availability depends on the binding affinity of cellular membranes for Mg2+. The difference between survival and multiplication is postulated to be in the intensity and duration rather than the kind of stimulus.

摘要

在拥挤培养环境中的Balb/c3T3细胞,当血清被剥夺时会从培养皿上脱离,存活的细胞以较低的速率掺入³H-胸腺嘧啶核苷。血清去除两小时后,细胞脱离现象变得明显,并在两到四小时之间达到最大速率。稀疏培养的细胞不会因血清去除而脱离,其³H-胸腺嘧啶核苷掺入速率仅略有降低。随着稀疏培养物生长为更拥挤的培养物且血清耗尽,越来越多的细胞脱离。当将脱离的细胞置于含有充足新鲜血清的新培养皿中时,它们无法重新附着。这些细胞对细胞成分有渗漏现象,似乎已经死亡。细胞脱离是细胞死亡的结果而非原因,并且可以由抑制细胞能量代谢的物质产生。在血清剥夺后存活在培养皿上的细胞是完全有活力的,当添加血清时它们会迅速生长。当它们变得拥挤时,它们对血清剥夺的敏感性与原始细胞群体相同。因此,它们并非因为对血清需求低而被选择存活,而是显然因为它们扩散到脱离细胞腾出的空间中,然后在血清变化时表现得像稀疏培养物一样而存活下来。钙离子和焦磷酸的不溶性复合物(Ca²⁺-PPi)在促进细胞存活方面表现出与刺激³H-胸腺嘧啶核苷掺入相同的浓度依赖性,表明单一物质可负责这两种活性。得出的结论是,存活和生长是3T3细胞对单一外部效应物的协同反应的一部分。根据一个简单模型对结果进行了讨论,在该模型中,协同反应由细胞内用于转磷酸化反应的镁离子可用性调节,而这种可用性取决于细胞膜对镁离子的结合亲和力。存活和增殖之间的差异被假定在于刺激的强度和持续时间而非刺激的种类。

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