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Spatial and temporal aspects of cellular calcium signaling
Author(s) -
Thomas Andrew P.,
Bird Gary St. J.,
Hajnóczky György,
RobbGaspers Lawrence D.,
Putney James W.
Publication year - 1996
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.10.13.8940296
Subject(s) - gating , intracellular , oscillation (cell signaling) , cytosol , calcium signaling , biophysics , stimulation , neuroscience , agonist , chemistry , biology , microbiology and biotechnology , receptor , biochemistry , enzyme
Cytosolic Ca 2+ signals are often organized in complex temporal and spatial patterns, even under conditions of sustained stimulation. In this review we discuss the mechanisms and physi‐ological significance of this behavior in nonexcitable cells, in which the primary mechanism of Ca 2+ mobilization is through (l,4,5)IP3‐dependent Ca 2+ release from intracellular stores. Oscillations of cytosolic free Ca 2+ ([Ca 2+ ]i) are a common form of temporal organization; in the spatial domain, these [Ca 2+ ]i oscillations may take the form of [Ca 2+ ]i waves that propagate throughout the cell or they may be restricted to specific subcellular regions. These patterns of Ca 2+ signaling result from the limited range of cytoplasmic Ca 2+ diffusion and the feedback regulation of the pathways responsible for Ca 2+ mo‐bilization. In addition, the spatial organization of [Ca 2+ ]i changes appears to depend on the strategic distribution of Ca 2+ stores within the cell. One type of [Ca 2+ ]i oscillation is baseline spiking, in which discrete [Ca 2+ ]i spikes occur with a frequency, but not amplitude, that is determined by agonist dose. Most current evidence favors a model in which baseline [Ca 2+ ]i spiking results from the complex interplay between [Ca 2+ ]i and (1,4,5)IP3 in regulating the gating of (l,4,S)IP3‐sensitive intracellular Ca 2+ channels. Sinusoidal [Ca 2+ ]i oscillations represent a mechanistically distinct type of temporal organiza‐tion, in which agonist dose regulates the amplitude but has no effect on oscillation frequency. Sinusoidal [Ca 2+ ]i oscillations can be explained by a negative feedback effect of protein kinase C on the generation of (l,4,S)IP3 at the level of phospholipase C or its activating G‐protein. The physiological significance of [Ca 2+ ]i oscillations and waves is becoming more established with the observation of this behavior in intact tissues and by the recognition of Ca 2+ ‐dependent processes that are adapted to respond to fre‐ quency‐modulated oscillatory [Ca 2+ ]i signals. In some cells, these [Ca 2+ ]i signals are targeted to control processes in limited cytoplasmic domains, and in other systems [Ca 2+ ]i waves can be propagated through gap junctions to coordinate the function of multicellular systems.—Thomas, A. P., Bird, G. S. J., Hajnóczky, G., Robb‐Gaspers, L. D., Putney, J. W., Jr. Spatial and temporal aspects of cellular calcium signaling. FASEB J. 10, 1505‐1517 (1996)