Abstract
As evident in all of the chapters throughout this book, Ca2+ is an essential regulator of various cellular functions, including muscle contraction and the release of neurotransmitters and hormones. However, the question can be asked: How can a ubiquitous signal like Ca2+ generate so many different physiological responses while maintaining selectivity as a cellular signal? (Berridge, 1997b). Since the advent of Ca2+-sensitive fluorophores and fluorescence microscopy, researchers have been able to visualize Ca2+ signaling in living cells. These studies have revealed complexities in temporal and spatial regulation of Ca2+ signaling, which appear to hold the key to how Ca2+ can act as both a ubiquitous and selective signal (Berridge, 1997b). Furthermore, confocal and electron microscopy studies have shown that the locality of key Ca2+ transporters and the concentration of Ca2+ in sub-cellular compartments is not homogenous, with consequent physiological implications. In this chapter we will discuss the spatial and temporal complexities of Ca2+ signaling, in particular recent studies using confocal, multi-photon and high-speed fluorescence microscopy as well as “caged” regulators of intracellular Ca2+.
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Monteith, G.R., Dedov, V.N., Roufogalis, B.D. (2000). Calcium Complexities: New Fluorescence Techniques for Probing Mitochondria and Other Subcellular Compartments. In: Pochet, R., Donato, R., Haiech, J., Heizmann, C., Gerke, V. (eds) Calcium: The Molecular Basis of Calcium Action in Biology and Medicine. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0688-0_42
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