细胞内
呋喃-2
生物物理学
化学
细胞培养
反应杯
荧光
生物化学
生物
胞浆
酶
光学
遗传学
物理
作者
J. A. Robinson,N. Jenkins,N. A. Holman,Sarah J. Roberts‐Thomson,Gregory R. Monteith
出处
期刊:Journal of Biochemical and Biophysical Methods
[Elsevier]
日期:2004-03-01
卷期号:58 (3): 227-237
被引量:29
标识
DOI:10.1016/j.jbbm.2003.11.002
摘要
Transporters of Ca2+ are potential drug targets and Ca2+ is a useful signal in the assessment of G-protein-coupled receptor activation. Assays involving the assessment of intracellular Ca2+ using microplate readers most often use Ca2+ indicators which do not exhibit a spectra shift on Ca2+ binding (e.g. fluo-3). Indicators that do exhibit a spectral shift upon Ca2+ binding (e.g. fura-2) offer potential advantages for the calibration of intracellular Ca2+ levels. However, experimental limitations may limit the use of ratiometric dyes in microplate readers capable of screening. In this study, we compared the assessment of intracellular Ca2+ in adherent breast cancer cells using ratiometric and nonratiometric Ca2+ indicators. Our results demonstrate that both fluo-3 and fura-2 detect ATP dose-dependent increases in intracellular Ca2+ in the MCF-7 breast cancer cell line and that some of the limitations in the use of fura-2 appear to be overcome by the use of glass bottom microplates. The calibrated intracellular Ca2+ levels derived using fura-2 are consistent with those from microscopy and cuvette-based studies. Fura-2 may be useful in microplate studies, where cell lines with different properties are compared or where screening treatments lead to differences in the number of cells or dye loading.
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