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决定能量剥夺细胞存活或死亡的细胞内钙离子阈值。

Intracellular Ca2+ thresholds that determine survival or death of energy-deprived cells.

作者信息

Dong Z, Saikumar P, Griess G A, Weinberg J M, Venkatachalam M A

机构信息

Department of Pathology, University of Texas Health Science Center at San Antonio, 78284-7750, USA.

出版信息

Am J Pathol. 1998 Jan;152(1):231-40.

Abstract

Increase of intracellular ionized or free Ca2+ is thought to play a central role in cell death due to ATP depletion. However, concurrently operative mechanisms of injury that do not require intracellular Ca2+ increases have made it difficult to test this hypothesis or to determine the concentrations at which intracellular Ca2+ becomes lethal. The predominant Ca2+-independent mechanism of injury during ATP depletion involves the loss of cellular glycine. This type of damage can be fully inhibited by adding the amino acid exogenously. Using glycine to suppress Ca2+-independent plasma membrane damage, we have examined the effect of intracellular Ca2+ elevations on cell viability during ATP depletion. Madin-Darby canine kidney (MDCK) cells were depleted of ATP by incubation with a mitochondrial uncoupler in glucose-free medium. Free Ca2+ concentration in the medium was varied between 26 nmol/L and 1.25 mmol/L in the presence of a Ca2+ ionophore. Measurements with the Ca2+ probes fura-2, furaptra, and fura-2FF showed that intracellular Ca2+ was clamped at extracellular levels under these conditions. Cell survival during ATP depletion was indicated by viable cells recovered 24 hours later. The results show that ATP-depleted cells can sustain high levels of intracellular Ca2+ (100 micromol/L) for prolonged periods and remain viable if plasma membrane damage is prevented by glycine. Cell death was observed only when intracellular free Ca2+ was allowed to increase beyond 100 micromol/L, and this was associated with dramatic nuclear alterations: chromatin condensation, loss of nuclear lamins, and breakdown of DNA into large 50- to 150-kb fragments. Our studies demonstrate unexpectedly high resistance of cells to calcium cytotoxicity if glycine that is lost during ATP depletion is restored. In addition, they provide insights into novel mechanisms of nuclear disintegration and DNA damage that are triggered when the high thresholds of intracellular Ca2+ required for cell death are exceeded.

摘要

细胞内离子化或游离Ca2+的增加被认为在因ATP耗竭导致的细胞死亡中起核心作用。然而,同时起作用的、不需要细胞内Ca2+增加的损伤机制使得难以检验这一假设或确定细胞内Ca2+变得致命的浓度。ATP耗竭期间主要的与Ca2+无关的损伤机制涉及细胞内甘氨酸的丢失。通过外源添加氨基酸,这种类型的损伤可被完全抑制。利用甘氨酸抑制与Ca2+无关的质膜损伤,我们研究了ATP耗竭期间细胞内Ca2+升高对细胞活力的影响。通过在无葡萄糖培养基中与线粒体解偶联剂孵育,使Madin-Darby犬肾(MDCK)细胞耗尽ATP。在存在Ca2+离子载体的情况下,培养基中的游离Ca2+浓度在26 nmol/L至1.25 mmol/L之间变化。用Ca2+探针fura-2、furaptra和fura-2FF进行的测量表明,在这些条件下细胞内Ca2+被钳制在细胞外水平。ATP耗竭期间的细胞存活通过24小时后回收的活细胞来指示。结果表明,ATP耗尽的细胞如果质膜损伤被甘氨酸阻止,能够长时间维持高水平的细胞内Ca2+(100 μmol/L)并保持存活。仅当细胞内游离Ca2+增加超过100 μmol/L时才观察到细胞死亡,这与显著的核改变相关:染色质凝聚、核纤层蛋白丢失以及DNA断裂成50至150 kb的大片段。我们的研究表明,如果恢复ATP耗竭期间丢失的甘氨酸,细胞对钙细胞毒性具有出乎意料的高抗性。此外,它们还深入了解了当超过细胞死亡所需的细胞内Ca2+高阈值时引发的核解体和DNA损伤的新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5a6/1858134/a35320fdfbc5/amjpathol00013-0227-a.jpg

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