Rubin H, Sanui H
Proc Natl Acad Sci U S A. 1977 Nov;74(11):5026-30. doi: 10.1073/pnas.74.11.5026.
Addition of 0.1-0.5 mM sodium PP(i) for 17 hr to confluent cultures of BALB/c 3T3 cells in low serum concentrations stimulated the incorporation of [(3)H]thymidine into DNA to an extent equal to that produced by high serum concentration. PP(i) prevented much but not all of the cell detachment that accompanies decreasing the serum concentration of confluent cultures and it increased the saturation density of cultures in high serum concentrations. The stimulation had a sharp concentration dependence and was associated with the appearance in the medium of a flocculent precipitate. Stimulation and precipitate formation were dependent on Ca(2+) and inorganic orthophosphate (HPO(4) (2-)) and were inhibited by Mg(2+). More than half the Ca(2+) requirement could be met with Sr(2+). In the absence of PP(i), supranormal concentrations of either Ca(2+) or HPO(4) (2-) caused graded increases in [(3)H]thymidine incorporation and total cell yield. The effect of supranormal [Ca(2+)] depended on [HPO(4) (2-)] and vice versa, and the Ca(2+) requirement could be partially met by Sr(2+). The stimulation was associated with increasing turbidity of the medium. Various other complexing agents of Ca(2+), including the divalent cation ionophore A 23187, failed to produce stimulation of 3T3 cells. We conclude that water insoluble complexes of PP(i), HPO(4) (2-), and Ca(2+) or, at much higher concentrations, the latter two together, stimulate 3T3 cells and we speculate that this is brought about by the association of these complexes with the cell membrane.
在低血清浓度下,向汇合的BALB/c 3T3细胞培养物中添加0.1 - 0.5 mM的焦磷酸钠(PP(i))17小时,可刺激[³H]胸苷掺入DNA,其程度与高血清浓度所产生的程度相当。PP(i)可防止汇合培养物血清浓度降低时出现的大部分但非全部细胞脱离现象,并且它增加了高血清浓度下培养物的饱和密度。这种刺激具有明显的浓度依赖性,并且与培养基中出现絮状沉淀有关。刺激和沉淀形成依赖于Ca²⁺和无机正磷酸盐(HPO₄²⁻),并受到Mg²⁺的抑制。超过一半的Ca²⁺需求可用Sr²⁺满足。在没有PP(i)的情况下,超正常浓度的Ca²⁺或HPO₄²⁻会导致[³H]胸苷掺入和总细胞产量的分级增加。超正常[Ca²⁺]的作用取决于[HPO₄²⁻],反之亦然,并且Ca²⁺需求可部分由Sr²⁺满足。这种刺激与培养基浊度增加有关。Ca²⁺的各种其他络合剂,包括二价阳离子载体A 23187,均未能对3T3细胞产生刺激作用。我们得出结论,PP(i)、HPO₄²⁻和Ca²⁺的水不溶性复合物,或者在高得多的浓度下,后两者一起,可刺激3T3细胞,并且我们推测这是由这些复合物与细胞膜的结合所导致的。