Farinelli S E, Greene L A
Department of Pathology, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
J Neurosci. 1996 Feb 1;16(3):1150-62. doi: 10.1523/JNEUROSCI.16-03-01150.1996.
In the present study, we tested whether apoptotic neuronal death caused by withdrawal of trophic support might be prevented by agents that block cell cycle progression. We used three complementary model systems that exhibit apoptotic death: dividing PC12 cells deprived of nerve growth factor (NGF); and primary cultures of postmitotic sympathetic neurons deprived of NGF. We show that cell death in each case can be suppressed by treatment with the G1/S blockers mimosine, ciclopirox, and deferoxamine at concentrations that correlate with their abilities to block PC12 cell proliferation. In contrast, agents that block cell cycle progression in the S-, G2-, or M-phase do not prevent cell death. These observations support the hypothesis that removal of trophic support from dividing or postmitotic neuronal cells provokes their apoptotic death by causing them either to proceed through or to attempt to re-enter an uncoordinated and consequently fatal cell cycle. Moreover, the data suggest that simply blocking the cycle at any point is not protective but, rather, that it is necessary to block at specific "safe" points. This study defines a safe point in the cell cycle before the G1/S transition that is demarcated by the action of these three agents.
在本研究中,我们测试了阻断细胞周期进程的药物是否能够预防因营养支持缺失所导致的凋亡性神经元死亡。我们使用了三种呈现凋亡性死亡的互补模型系统:缺乏神经生长因子(NGF)的分裂型PC12细胞;以及缺乏NGF的有丝分裂后交感神经元原代培养物。我们发现,在每种情况下,用G1/S期阻断剂含羞草碱、环匹罗司和去铁胺处理,细胞死亡均可被抑制,其浓度与它们阻断PC12细胞增殖的能力相关。相比之下,阻断S期、G2期或M期细胞周期进程的药物并不能预防细胞死亡。这些观察结果支持以下假说:从分裂型或有丝分裂后神经元细胞中去除营养支持,会导致它们进入或试图重新进入不协调的、因而致命的细胞周期,从而引发其凋亡性死亡。此外,数据表明,仅在细胞周期的任何一点进行阻断并无保护作用,相反,必须在特定的“安全”点进行阻断。本研究确定了在G1/S期转换之前细胞周期中的一个安全点,这是由这三种药物的作用所界定的。