Sarvazyan N, Swift L, Martinez-Zaguilan R
Department of Physiology, Texas Tech University Health Sciences Center, Lubbock 79430, USA.
Arch Biochem Biophys. 1998 Feb 1;350(1):132-6. doi: 10.1006/abbi.1997.0518.
An increasing number of studies use calcium-sensitive fluorescent dyes to address the relationship between elevated levels of intracellular calcium and free-radical-mediated damage in a variety of pathophysiological phenomena. The present study evaluates the effects of reactive oxygen species on the spectral properties of widely used calcium probes such as Fura-2 and Fluo-3. We found that both Fura-2 and Fluo-3 are rapidly inactivated by hydroxyl radicals and enzymatically inactivated by peroxidase/H2O2. This results in a decrease in the dynamic range of sensitivity of both dyes to Ca2+, as well as in a decrease in the affinity of Fluo-3 for Ca2+. The data suggest that oxidation of the calcium probes affects the measurement of calcium in vitro and may alter the interpretation of in vivo data since the absence of or small changes in the calcium fluorescence signal can be the result of probe deactivation by free oxygen radicals rather than the lack of actual Ca2+ changes.
越来越多的研究使用钙敏荧光染料来探讨细胞内钙水平升高与各种病理生理现象中自由基介导的损伤之间的关系。本研究评估了活性氧对广泛使用的钙探针(如Fura-2和Fluo-3)光谱特性的影响。我们发现Fura-2和Fluo-3都能被羟基自由基迅速灭活,并被过氧化物酶/H2O2酶促灭活。这导致两种染料对Ca2+的动态灵敏度范围降低,以及Fluo-3对Ca2+的亲和力降低。数据表明,钙探针的氧化会影响体外钙的测量,并可能改变体内数据的解释,因为钙荧光信号的缺失或微小变化可能是由于游离氧自由基使探针失活,而不是实际Ca2+变化所致。