Abstract
Tight control of basal cytosolic Ca2+ concentration is essential for cell survival and to fine-tune Ca2+-dependent cell functions. A way to control this basal cytosolic Ca2+ concentration is to regulate membrane Ca2+ channels including store-operated Ca2+ channels and secondary messenger-operated channels linked to G-protein-coupled or tyrosine kinase receptor activation. Orai, with or without its reticular STIM partner and Transient Receptor Potential (TRP) proteins, were considered to be the main Ca2+ channels involved. It is well accepted that, in response to cell stimulation, opening of these Ca2+ channels contributes to Ca2+ entry and the transient increase in cytosolic Ca2+ concentration involved in intracellular signaling. However, in various experimental conditions, Ca2+ entry and/or Ca2+ currents can be recorded at rest, without application of any experimental stimulation. This led to the proposition that some plasma membrane Ca2+ channels are already open/activated in basal condition, contributing therefore to constitutive Ca2+ entry. This article focuses on direct and indirect observations supporting constitutive activity of channels belonging to the Orai and TRP families and on the mechanisms underlying their basal/constitutive activities.
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- ARC:
-
Arachidonate-regulated Ca2+
- BKCa:
-
Big-conductance Ca2+-activated K+ channels
- B-SOCE:
-
Basal store-operated calcium entry
- CaV3.2:
-
Voltage-gated Ca2+ channel 3.2
- CRAC:
-
Ca2+ release-activated Ca2+
- GPCR:
-
G-protein-coupled receptor
- hEAG1:
-
Human ether à go-go K+ channel 1
- IKCa:
-
Intermediate conductance Ca2+-activated K+ channels
- LPA:
-
Lysophosphatidic acid
- LPC:
-
Lysophosphatidylcholine
- NVG-Ca2+ channel:
-
Non-voltage-gated Ca2+ channel
- P2X:
-
Purinergic ionotropic receptor
- R-SOCE:
-
Receptor-triggered store-operated Ca2+ entry influx
- SPCA:
-
Secretory pathway Ca2+-ATPase
- SKCa:
-
Small-conductance Ca2+-activated K+ channels
- SMOC:
-
Secondary messenger-operated channels
- STIM:
-
Stromal interaction molecule
- SAC:
-
Stretch-activated channels
- SOC:
-
Store-operated channels
- TRPC:
-
Transient receptor potential canonical
- TRPM7:
-
Transient receptor potential melastatin-related 7
- TRPV:
-
Transient receptor potential vanilloid
- VOCC:
-
Voltage-operated calcium channels
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Acknowledgements
This work was supported by la Ligue Contre le Cancer (comités des régions Bretagne, Pays de la Loire, Centre, and Poitou-Charentes), Region Centre (LIPIDS project of ARD2020-Biomédicaments), Inserm, CNRS, Cancéropôle Grand Ouest, the association “CANCEN”, Tours’ Hospital oncology association ACORT, Fondation ARC, ANR (ANR-12-JSV2-0004-001), Biosit, University of Brest, University of Rennes 1, University of Poitiers, University of Tours, and Roche-SFD.
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Special Issue: Ion Channels, Transporters, and Cancer.
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Mignen, O., Constantin, B., Potier-Cartereau, M. et al. Constitutive calcium entry and cancer: updated views and insights. Eur Biophys J 46, 395–413 (2017). https://doi.org/10.1007/s00249-017-1216-8
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DOI: https://doi.org/10.1007/s00249-017-1216-8
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