Twenty years of calcium imaging: Cell physiology to dye for

被引:34
作者
Knot, HJ [1 ]
Laher, I
Sobie, EA
Guatimosim, S
Gomez-Viquez, L
Hartmann, H
Song, LS
Lederer, WJ
Graier, WF
Malli, R
Frieden, M
Petersen, OH
机构
[1] Univ British Columbia, Dept Pharmacol & Therapeut, Vancouver, BC V6T 1W5, Canada
[2] Univ Florida, Coll Med, Dept Pharmacol & Therapeut, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Med, Div Cardiol, Gainesville, FL USA
[4] Univ Maryland, Maryland Biotechnol Inst, Ctr Med Biotechnol, Baltimore, MD 21201 USA
[5] Med Univ Graz, Inst Mol Biol & Biochem, Graz, Austria
[6] Univ Geneva, Med Ctr, Dept Cell Physiol & Metab, CH-1211 Geneva, Switzerland
[7] Univ Liverpool, Physiol Lab, Liverpool L69 3BX, Merseyside, England
基金
奥地利科学基金会;
关键词
D O I
10.1124/mi.5.2.8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of fluorescent dyes over the past two decades has led to a revolution in our understanding of calcium signaling. Given the ubiquitous role of Ca2+ in signal transduction at the most fundamental levels of molecular, cellular, and organismal biology, it has been challenging to understand how the specificity and versatility of Ca2+ signaling is accomplished. In excitable cells, the coordination of changing Ca2+ concentrations at global (cellular) and well-defined subcellular spaces through the course of membrane depolarization can now be conceptualized in the context of disease processes such as cardiac arrhythmogenesis. The spatial and temporal dimensions of Ca2+ signaling are similarly important in non-excitable cells, such as endothelial and epithelial cells, to regulate multiple signaling pathways that participate in organ homeostasis as well as cellular organization and essential secretory processes.
引用
收藏
页码:112 / 127
页数:16
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