Measurement of intracellular calcium

被引:587
作者
Takahashi, A
Camacho, P
Lechleiter, JD
Herman, B
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Physiol, San Antonio, TX 78229 USA
[3] Univ Texas, Hlth Sci Ctr, Inst Biotechnol, Dept Mol Med, San Antonio, TX 78229 USA
关键词
D O I
10.1152/physrev.1999.79.4.1089
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
To a certain extent, all cellular, physiological, and pathological phenomena that occur in cells are accompanied by ionic changes. The development of techniques allowing the measurement of such ion activities has contributed substantially to our understanding of normal and abnormal cellular function. Digital video microscopy, confocal laser scanning microscopy, and more recently multiphoton microscopy have allowed the precise spatial analysis of intracellular ion activity at the subcellular level in addition to measurement of its concentration. It is well known that Ca2+ regulates numerous physiological cellular phenomena as a second messenger as well as triggering pathological events such as cell injury and death. A number of methods have been developed to measure intracellular Ca2+. In this review, we summarize the advantages and pitfalls of a variety of Ca2+ indicators used in both optical and nonoptical techniques employed for measuring intracellular Ca2+ concentration.
引用
收藏
页码:1089 / 1125
页数:37
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