Boynton A L, Whitfield J F, Isaacs R J
J Cell Physiol. 1976 Jan;87(1):25-32. doi: 10.1002/jcp.1040870105.
During the first six passages after their arrival in this laboratory, BALB/c 3T3 mouse cells did not proliferate in serum containing-medium having an ionic calcium concentration of 0.05 mM or less, but by the ninth passage they had become able to multiply in the presence of these lower calcium levels. In low calcium (e.g., 0.02 mM) medium, passage 1-6, cells in sparse cultures were blocked at the Gl/S boundary of their cycle. These blocked cells could be induced to start making DNA within only one hour either by returning the ionic calcium level to a normal range of values (1.25 mM), or by adding 0.05 mug/ml of PMA (12-O-tetradecanoyl-phorbol-13-acetate). PMA probably acted by sensitizing the blocked cells to calcium rather than replacing the ion, because it was ineffective in ionic calcium-free medium. Finally, PMA did not by itself induce proliferation of cells (regardless of the number of passages) which had been proliferatively inactivated by density-dependent factors in confluent cultures. However, PMA did promote DNA synthesis by these cells during their brief transition to the "cycling" state caused by exposure to fresh serum-containing medium.
在抵达本实验室后的前六次传代过程中,BALB/c 3T3小鼠细胞在离子钙浓度为0.05 mM或更低的含血清培养基中不增殖,但到第九代时,它们已能够在这些较低钙水平下增殖。在低钙(如0.02 mM)培养基中,传代1-6时,稀疏培养物中的细胞在其细胞周期的G1/S边界处受阻。这些受阻细胞可以通过将离子钙水平恢复到正常范围值(1.25 mM),或添加0.05 μg/ml的佛波酯(12-O-十四酰佛波醇-13-乙酸酯,PMA),在仅一小时内被诱导开始合成DNA。PMA可能是通过使受阻细胞对钙敏感而起作用,而不是替代离子,因为它在无离子钙的培养基中无效。最后,PMA本身不会诱导已在汇合培养物中因密度依赖性因子而增殖失活的细胞(无论传代数)增殖。然而,在这些细胞短暂过渡到因暴露于新鲜含血清培养基而导致的“循环”状态期间,PMA确实促进了它们的DNA合成。