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细胞内钙的测量。

Measurement of intracellular calcium.

作者信息

Takahashi A, Camacho P, Lechleiter J D, Herman B

机构信息

Department of Cellular and Structural Biology, Institute of Biotechnology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229-3900, USA.

出版信息

Physiol Rev. 1999 Oct;79(4):1089-125. doi: 10.1152/physrev.1999.79.4.1089.

Abstract

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.

摘要

在一定程度上,细胞内发生的所有细胞、生理和病理现象都伴随着离子变化。能够测量此类离子活性的技术发展,极大地促进了我们对正常和异常细胞功能的理解。数字视频显微镜、共聚焦激光扫描显微镜,以及最近的多光子显微镜,除了能够测量细胞内离子浓度外,还能在亚细胞水平对细胞内离子活性进行精确的空间分析。众所周知,Ca2+作为第二信使调节众多生理细胞现象,同时引发诸如细胞损伤和死亡等病理事件。已经开发出多种测量细胞内Ca2+的方法。在本综述中,我们总结了用于测量细胞内Ca2+浓度的光学和非光学技术中所使用的各种Ca2+指示剂的优缺点。

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