Pharmacology of store-operated calcium channels.

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Molecular Interventions

• Publication date

  2010-08-01

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1124/mi.10.4.4PMID 20729487PMCID PMC2965610
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Two novel 2-aminoethyl diphenylborinate (2-APB) analogues differentially activate and inhibit store-operated Ca(2+) entry via STIM proteins.

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• Synthesis of bisboron compounds and their strong inhibitory activity on store-operated calcium entry.

  2010cited by this paper
• Mechanistic view on domains mediating STIM1–Orai coupling

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• STIM1 clusters and activates CRAC channels via direct binding of a cytosolic domain to Orai1.

  2009cited by this paper
• Orai1, a critical component of store-operated Ca2+ entry, is functionally associated with Na+/Ca2+ exchanger and plasma membrane Ca2+ pump in proliferating human arterial myocytes.

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• SOAR and the polybasic STIM1 domains gate and regulate the Orai channels

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• Small‐Molecule Inhibitors of Store‐Operated Calcium Entry

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• STIM1 and calmodulin interact with Orai1 to induce Ca2+-dependent inactivation of CRAC channels

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• ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.

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• Evidence for STIM1‐ and Orail‐dependent storeoperated calcium influx through ICRAC in vascular smooth muscle cells: role in proliferation and migration

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• A Ca2+ Release-activated Ca2+ (CRAC) Modulatory Domain (CMD) within STIM1 Mediates Fast Ca2+-dependent Inactivation of ORAI1 Channels*♦

  2009cited by this paper
• TRPC channels function independently of STIM1 and Orai1

  2009cited by this paper
• A Cytosolic Homomerization and a Modulatory Domain within STIM1 C Terminus Determine Coupling to ORAI1 Channels*

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• Orai1 and STIM1 are critical for breast tumor cell migration and metastasis.

  2009cited by this paper
• Phosphorylation of STIM1 underlies suppression of store-operated calcium entry during mitosis

  2009cited by this paper
• A minimal regulatory domain in the C terminus of STIM1 binds to and activates ORAI1 CRAC channels.

  2009cited by this paper
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  2009cited by this paper
• Targeting Gut T Cell Ca2+ Release-Activated Ca2+ Channels Inhibits T Cell Cytokine Production and T-Box Transcription Factor T-Bet in Inflammatory Bowel Disease

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• TRPC channels as STIM1-regulated SOCs

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• Local Ca2+ influx through CRAC channels activates temporally and spatially distinct cellular responses

  2009cited by this paper
• Structural determinants of ion permeation in CRAC channels

  2009cited by this paper
• Dynamic Coupling of the Putative Coiled-coil Domain of ORAI1 with STIM1 Mediates ORAI1 Channel Activation*

  2008cited by this paper
• Methods for studying store-operated calcium entry.

  2008cited by this paper
• Stim1 and Orai1 Mediate CRAC Currents and Store-Operated Calcium Entry Important for Endothelial Cell Proliferation

  2008cited by this paper
• Ca2+-store-dependent and -independent reversal of Stim1 localization and function

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• Complex Actions of 2-Aminoethyldiphenyl Borate on Store-operated Calcium Entry*

  2008cited by this paper
• Sustained Activation of the Tyrosine Kinase Syk by Antigen in Mast Cells Requires Local Ca2+ Influx through Ca2+ Release-activated Ca2+ Channels*

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• Hair Loss and Defective T- and B-Cell Function in Mice Lacking ORAI1

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• Isoform-specific Inhibition of TRPC4 Channel by Phosphatidylinositol 4,5-Bisphosphate*

  2008cited by this paper
• Defective mast cell effector functions in mice lacking the CRACM1 pore subunit of store-operated calcium release–activated calcium channels

  2008cited by this paper
• 2‐Aminoethoxydiphenyl borate directly facilitates and indirectly inhibits STIM1‐dependent gating of CRAC channels

  2008cited by this paper
• 2-Aminoethoxydiphenyl Borate Alters Selectivity of Orai3 Channels by Increasing Their Pore Size*

  2008cited by this paper
• Cytoplasmic calcium oscillations and store‐operated calcium influx

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• Orai, STIM1 and iPLA2β: a view from a different perspective

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• Store-dependent and -independent Modes Regulating Ca2+ Release-activated Ca2+ Channel Activity of Human Orai1 and Orai3*

  2008cited by this paper
• Biochemical properties and cellular localisation of STIM proteins.

  2007cited by this paper
• CRACM1, CRACM2, and CRACM3 are store-operated Ca2+ channels with distinct functional properties.

  2007cited by this paper
• Orai1 Mutations Alter Ion Permeation and Ca2+-dependent Fast Inactivation of CRAC Channels: Evidence for Coupling of Permeation and Gating

  2007cited by this paper
• Molecular basis of the CRAC channel.

  2007cited by this paper
• Live-cell imaging reveals sequential oligomerization and local plasma membrane targeting of stromal interaction molecule 1 after Ca2+ store depletion

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• Role of the microtubule cytoskeleton in the function of the store-operated Ca2+ channel activator STIM1

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• Signalling to transcription: store-operated Ca2+ entry and NFAT activation in lymphocytes.

  2007cited by this paper
• Store-Operated Orai1 and IP3 Receptor-Operated TRPC1 Channel: Separation of the Siamese Twins

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• Mapping the Interacting Domains of STIM1 and Orai1 in Ca2+ Release-activated Ca2+ Channel Activation*

  2007cited by this paper
• Large Store-operated Calcium Selective Currents Due to Co-expression of Orai1 or Orai2 with the Intracellular Calcium Sensor, Stim1*

  2006cited by this paper
• Orai1 and STIM Reconstitute Store-operated Calcium Channel Function*

  2006cited by this paper
• Layers of organization of cAMP microdomains in a simple cell.

  2006cited by this paper
• Amplification of CRAC current by STIM1 and CRACM1 (Orai1)

  2006cited by this paper
• Aggregation of STIM1 underneath the plasma membrane induces clustering of Orai1.

  2006cited by this paper
• Orai1 is an essential pore subunit of the CRAC channel

  2006cited by this paper
• Protection of TRPC7 cation channels from calcium inhibition by closely associated SERCA pumps

  2006cited by this paper
• A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function

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• Molecular identification of the CRAC channel by altered ion selectivity in a mutant of Orai

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• A Pyrazole Derivative Potently Inhibits Lymphocyte Ca2+ Influx and Cytokine Production by Facilitating Transient Receptor Potential Melastatin 4 Channel Activity

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• CRACM1 multimers form the ion-selective pore of the CRAC channel.

  2006cited by this paper
• Genome-wide RNAi screen of Ca(2+) influx identifies genes that regulate Ca(2+) release-activated Ca(2+) channel activity.

  2006cited by this paper
• CRACM1 Is a Plasma Membrane Protein Essential for Store-Operated Ca2+ Entry

  2006cited by this paper
• Mechanism of Inhibition of TRPC Cation Channels by 2-Aminoethoxydiphenylborane

  2005cited by this paper
• A Functional Link between Store-operated and TRPC Channels Revealed by the 3,5-Bis(trifluoromethyl)pyrazole Derivative, BTP2*

  2005cited by this paper
• Store-operated calcium channels.

  2005cited by this paper
• CIF and other mysteries of the store-operated Ca2+-entry pathway.

  2005cited by this paper
• TRPM4 Regulates Calcium Oscillations After T Cell Activation

  2004cited by this paper
• Potent Inhibition of Ca2+ Release-activated Ca2+ Channels and T-lymphocyte Activation by the Pyrazole Derivative BTP2*

  2004cited by this paper
• Cytoskeletal Reorganization Internalizes Multiple Transient Receptor Potential Channels and Blocks Calcium Entry into Human Neutrophils 1

  2004cited by this paper
• Close Functional Coupling between Ca2+ Release-activated Ca2+ Channels, Arachidonic Acid Release, and Leukotriene C4 Secretion*

  2004cited by this paper
• The enigmatic TRPCs: multifunctional cation channels.

  2004cited by this paper
• Development of genetically encoded fluorescent indicators for calcium.

  2003cited by this paper
• A Pyrazole Derivative, YM-58483, Potently Inhibits Store-Operated Sustained Ca2+ Influx and IL-2 Production in T Lymphocytes

  2003cited by this paper
• Modification of Store-operated Channel Coupling and Inositol Trisphosphate Receptor Function by 2-Aminoethoxydiphenyl Borate in DT40 Lymphocytes*

  2002cited by this paper
• TH1 and TH2 cytokine inhibition by 3,5-bis(trifluoromethyl)pyrazoles, a novel class of immunomodulators.

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• The PDZ-interacting domain of TRPC4 controls its localization and surface expression in HEK293 cells.

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• 2‐Aminoethoxydiphenyl borate (2‐APB) is a reliable blocker of store‐operated Ca2+ entry but an inconsistent inhibitor of InsP3‐induced Ca2+ release

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• Potent Inhibition of NFAT Activation and T Cell Cytokine Production by Novel Low Molecular Weight Pyrazole Compounds*

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• Potentiation and inhibition of Ca2+ release‐activated Ca2+ channels by 2‐aminoethyldiphenyl borate (2‐APB) occurs independently of IP3 receptors

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• Stable Activation of Single Ca2+ Release-activated Ca2+ Channels in Divalent Cation-free Solutions*

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• Role of the Phospholipase C-Inositol 1,4,5-Trisphosphate Pathway in Calcium Release-activated Calcium Current and Capacitative Calcium Entry*

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• 2-Aminoethoxydiphenyl borate (2-APB) inhibits capacitative calcium entry independently of the function of inositol 1,4,5-trisphosphate receptors.

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• Myosin Light Chain Kinase Regulates Capacitative Ca2+ Entry in Human Monocytes/Macrophages

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• 2-Aminoethoxydiphenyl borate directly inhibits store-operated calcium entry channels in human platelets.

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• Evidence that 2-aminoethyl diphenylborate is a novel inhibitor of store-operated Ca2+ channels in liver cells, and acts through a mechanism which does not involve inositol trisphosphate receptors.

  2001cited by this paper
• An examination of the secretion‐like coupling model for the activation of the Ca2+ release‐activated Ca2+ current ICRAC in RBL‐1 cells

  2001cited by this paper
• Pharmacology of capacitative calcium entry.

  2001cited by this paper
• Requirement of the inositol trisphosphate receptor for activation of store-operated Ca2+ channels.

  2000cited by this paper
• STIM1: a novel phosphoprotein located at the cell surface.

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• Impaired NFAT regulation and its role in a severe combined immunodeficiency.

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• A non‐capacitative pathway activated by arachidonic acid is the major Ca2+ entry mechanism in rat A7r5 smooth muscle cells stimulated with low concentrations of vasopressin

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• Role of the Cytoskeleton in Calcium Signaling in NIH 3T3 Cells

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• Severe combined immunodeficiency due to defective binding of the nuclear factor of activated T cells in T lymphocytes of two male siblings

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• On the molecular basis and regulation of cellular capacitative calcium entry: roles for Trp proteins.

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• Inhibition of agonist-induced Ca2+ entry in endothelial cells by myosin light-chain kinase inhibitor.

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• Pharmacological and functional properties of voltage-independent Ca2+ channels.

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• Capacitative calcium entry.

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• Ionomycin enhances Ca2+ influx by stimulating store-regulated cation entry and not by a direct action at the plasma membrane.

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• Mitogen-regulated Ca2+ current of T lymphocytes is activated by depletion of intracellular Ca2+ stores.

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• ‘Quanta’ Ca2+ release and the control of Ca2+ entry by inositol phosphates ‐ a possible mechanism

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