Yen A, Pardee A B
Science. 1979 Jun 22;204(4399):1315-7. doi: 10.1126/science.451539.
Swiss 3T3 cells arrested in B0 (quiescent state) by reducing serum content of the medium all contain the same amount of DNA but vary in nuclear volume over approximately a twofold range. By use of flow microfluorimetry, scatterplots of nuclear volume versus DNA content were obtained in intervals after serum stimulation. The earliest cells to enter DNA synthesis were those with the largest nuclei, whereas cells with the smallest nuclei were among the latest. Regulation of cellular transit from G0 to the S phase was therefore, at least in part, deterministic, since all G0 cells did not have equal probabilities of entry into S at a given moment. All cells having the same nuclear volume did not initiate DNA synthesis at the same moment; therefore, factors other than nuclear volume must also influence this timing. Nuclear volume correlated with the maximum rate at which cells could enter S. The kinetic model of the cell cycle postulating a probabilistic event as solely responsible for entry into S thus appears too simple.
通过降低培养基中的血清含量使瑞士3T3细胞停滞在B0期(静止状态),所有细胞的DNA含量相同,但核体积在大约两倍的范围内变化。利用流式细胞荧光测定法,在血清刺激后的不同时间间隔获得了核体积与DNA含量的散点图。最早进入DNA合成的细胞是那些核最大的细胞,而核最小的细胞则是最晚进入的。因此,细胞从G0期到S期的过渡调节至少部分是确定性的,因为并非所有G0期细胞在给定时刻进入S期的概率都相等。所有具有相同核体积的细胞并非同时开始DNA合成;因此,除核体积外的其他因素也必定影响这个时间。核体积与细胞进入S期的最大速率相关。假设进入S期仅由概率事件决定的细胞周期动力学模型因此显得过于简单。