Rasmussen M, Rasmussen L
Institute of Medical Biology, Department of Cell Biology, Odense University, Denmark.
Cell Biochem Funct. 2000 Jun;18(2):133-9. doi: 10.1002/(SICI)1099-0844(200006)18:2<133::AID-CBF868>3.0.CO;2-X.
We made three kinds of experiments in order to elucidate aspects of physiological mechanisms involved in a series of specific events leading to either cell death or survival in the lag phase of culture growth. We studied the fate of newly inoculated Tetrahymena cells in small droplets at 'high' (more than 1000 cells ml(-1)) and 'low' cell densities (less than 600 cells ml(-1)) in a nutrionally complete, synthetic nutrient medium. Confirming previous results we found that the cells in high-density cultures multiplied to final densities around 500,000 cells ml(-1) and that cells in low-density cultures died before multiplying. The appearance of the cells was recorded with a video camera at 20 frames per second for 6 h or until they died. The results indicated that the death process took place within milliseconds. We also studied the effects of U 73122, an inhibitor of the phosphatidylinositol-specific phospholipase C, on cell survival at low densities. At low inhibitor concentrations low-density cells were rescued from dying. At high inhibitor concentrations all cells died, and phosphatidylinositol - but not phosphatidylserine and phosphatidylcholine - saved them. The results indicate that the paths leading to either cell death or to cell proliferation separate within the first few minutes after subcultivation into a new medium, since the first cells in each culture died within 4-30 min after inoculation. Our results also indicate that some PLC activity was required for stimulation of phospholipase D, and that cell death during the early lag phase is caused by a shortage in phosphatidylinositol before the phospholipase D activity is upregulated. These experiments are shedding light on the lethal consequences of a cellular depletion of the important signalling compound phosphatidylinositol in an in vivo system, and may help to elucidate mechanisms behind the century-old fact that eukaryote cells die when inoculated at too low a cell density to survive.
为了阐明在培养生长的延迟期导致细胞死亡或存活的一系列特定事件所涉及的生理机制的各个方面,我们进行了三种实验。我们研究了新接种的四膜虫细胞在营养完全的合成营养培养基中处于“高”(超过1000个细胞/毫升)和“低”细胞密度(低于600个细胞/毫升)的小液滴中的命运。证实先前的结果,我们发现高密度培养中的细胞增殖至最终密度约为500,000个细胞/毫升,而低密度培养中的细胞在增殖前死亡。用摄像机以每秒20帧的速度记录细胞外观6小时或直到它们死亡。结果表明死亡过程在几毫秒内发生。我们还研究了磷脂酰肌醇特异性磷脂酶C的抑制剂U 73122对低密度细胞存活的影响。在低抑制剂浓度下,低密度细胞免于死亡。在高抑制剂浓度下,所有细胞死亡,而磷脂酰肌醇 - 但不是磷脂酰丝氨酸和磷脂酰胆碱 - 挽救了它们。结果表明,在转入新培养基后的最初几分钟内,导致细胞死亡或细胞增殖的途径就分开了,因为每种培养物中的第一批细胞在接种后4 - 30分钟内死亡。我们的结果还表明,刺激磷脂酶D需要一些PLC活性,并且早期延迟期的细胞死亡是由磷脂酶D活性上调之前磷脂酰肌醇的短缺引起的。这些实验正在揭示体内系统中重要信号化合物磷脂酰肌醇细胞耗竭的致命后果,并可能有助于阐明一个世纪以来的事实背后的机制,即真核细胞在接种细胞密度过低而无法存活时会死亡。