Hypoxia Causes Downregulation of Protein and RNA Synthesis in Noncontracting Mammalian Cardiomyocytes

T. Casey, Julian L. Pakay, M. Guppy, P. Arthur
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引用次数: 60

Abstract

The aim was to identify energy-consuming processes, other than contraction, downregulated during moderate hypoxia (≈5 &mgr;mol/L, 0.5% O2) and severe hypoxia (<0.5 &mgr;mol/L, <0.05% O2) in isolated neonatal cardiomyocytes. The metabolic response of cardiomyocytes to moderate and severe hypoxia was assessed by measuring rates of energy consumption and energetic status of cells maintained under these conditions. We found that the rates of energy production were decreased during both forms of hypoxia. Decreased rates of energy production under moderate hypoxia were associated with reduced energy wastage through a downregulation of proton leak in the mitochondria. Cellular protein synthesis and RNA synthesis, major energy-consuming pathways, were downregulated only during severe hypoxia, when oxygen concentrations were low enough to induce energetic stress (quantitatively defined as being any situation in which phosphocreatine concentrations had fallen by ≥40%). Our results suggest that energetic stress is the signal responsible for this downregulation.
缺氧导致非收缩哺乳动物心肌细胞蛋白和RNA合成下调
目的是确定除收缩外,在分离的新生儿心肌细胞中度缺氧(≈5 mol/L, 0.5% O2)和重度缺氧(<0.5 mol/L, <0.05% O2)期间下调的能量消耗过程。通过测量能量消耗率和在这些条件下维持的细胞能量状态来评估心肌细胞对中度和重度缺氧的代谢反应。我们发现,在两种形式的缺氧中,能量产生的速率都降低了。在中度缺氧条件下,能量产生率的降低与线粒体中质子泄漏的下调有关。细胞蛋白质合成和RNA合成是主要的能量消耗途径,只有在严重缺氧时,当氧浓度低到足以诱导能量应激时(定量定义为磷酸肌酸浓度下降≥40%的任何情况),细胞蛋白质合成和RNA合成才下调。我们的研究结果表明,能量压力是导致这种下调的信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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