Asai Masayoshi, Takeuchi Kazuhiko, Uchida Shinya, Urushida Tsuyoshi, Katoh Hideki, Satoh Hiroshi, Yamada Shizuo, Hayashi Hideharu, Watanabe Hiroshi
Internal Medicine III, Department of Clinical Pharmacology and Therapeutics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 2008 Jun;377(4-6):423-7. doi: 10.1007/s00210-007-0243-x. Epub 2008 Jan 29.
Due to its high sensitivity, reproducibility and reliability, fura-2 is one of the most preferred tools to quantify Ca2+ levels. Recently, using fura-2/AM, some calcium channel blockers (CCBs) have been reported to have inhibitory effects on intracellular Ca2+ signaling even in nonexcitable cells that do not possess voltage-dependent Ca2+ channels (VDCC). Some CCBs are known to be photosensitive. Since photosensitive chemicals often have autofluorescent property, it is likely that CCBs with autofluorescence interfere with the fluorescent dye probes for Ca2+, which may cause misinterpretation of the results. The aim of this study was to clarify the characteristics of various CCBs on Ca2+ fluorescent probes and to identify proper fluorescent probes for each CCB to allow reliable Ca2+ measurement using endothelial cells (ECs), which possess no VDCC. Thapsigargin (TG, Ca2+-ATPase inhibitor on endoplasmic reticulum) increased fura-2 F340/F380 ratio from 0.75+/-0.06 to 4.28+/-0.32, suggesting the increase in cytosolic Ca2+ concentrations in ECs. Verapamil, nifedipine and nicardipine did not affect TG-induced increase in fura-2 F340/F380 ratio; however, amlodipine dose dependently inhibited the rise of fura-2 ratio by 24% at 100 nM, by 55% at 1 microM and by 82% at 10 microM, respectively, in ECs. In ex vivo experiments without cells, due to the autofluorescence of amlodipine excited by ultraviolet (UV light), amlodipine itself boosted the intensity of F380 much more than it did that of F340, which results in a decrease in F340/F380 ratio of fura-2 fluorescence. Rhod-2/AM, a fluorescent probe of which the excitation wavelength is out of the excitation spectrum of amlodipine, showed that amlodipine did not affect TG-induced intracellular Ca2+ increase in ECs. When the effect of amlodipine on intracellular Ca2+ concentration is assessed, fura-2 fluorospectrometry should not be used due to fluorescent interaction between amlodipine and fura-2, and using rhod-2 is strongly recommended.
由于其高灵敏度、可重复性和可靠性,fura-2是用于定量Ca2+水平的最优选工具之一。最近,使用fura-2/AM,一些钙通道阻滞剂(CCB)已被报道即使在不具有电压依赖性Ca2+通道(VDCC)的非兴奋性细胞中也对细胞内Ca2+信号传导具有抑制作用。一些CCB已知是光敏性的。由于光敏化学物质通常具有自发荧光特性,具有自发荧光的CCB可能会干扰用于Ca2+的荧光染料探针,这可能导致结果的错误解读。本研究的目的是阐明各种CCB对Ca2+荧光探针的特性,并为每种CCB鉴定合适的荧光探针,以便使用不具有VDCC的内皮细胞(EC)进行可靠的Ca2+测量。毒胡萝卜素(TG,内质网上的Ca2+-ATP酶抑制剂)使fura-2 F340/F380比值从0.75±0.06增加到4.28±0.32,表明EC中细胞质Ca2+浓度增加。维拉帕米、硝苯地平和尼卡地平不影响TG诱导的fura-2 F340/F380比值增加;然而,氨氯地平在EC中分别在100 nM时剂量依赖性地抑制fura-2比值升高24%,在1 μM时抑制55%,在10 μM时抑制82%。在无细胞的体外实验中,由于氨氯地平在紫外线(UV光)激发下的自发荧光,氨氯地平本身增强F380的强度远超过其增强F340的强度,这导致fura-2荧光的F340/F380比值降低。Rhod-2/AM是一种激发波长不在氨氯地平激发光谱范围内的荧光探针,结果显示氨氯地平不影响TG诱导的EC中细胞内Ca2+增加。当评估氨氯地平对细胞内Ca2+浓度的影响时,由于氨氯地平和fura-2之间的荧光相互作用,不应使用fura-2荧光光谱法,强烈建议使用Rhod-2。