Literature DB >> 10699074

Ca2+ store dynamics determines the pattern of activation of the store-operated Ca2+ current I(CRAC) in response to InsP3 in rat basophilic leukaemia cells.

M D Glitsch1, A B Parekh.   

Abstract

1. The relationship between the amplitude of the store-operated Ca2+ ICR AC and intracellular inositol 1,4,5-triphosphate (InsP3) concentration is complex. In rat basophilic leukaemia (RBL-1) cells dialysed with high intracellular Ca2+ buffer, the relationship is supra-linear with a Hill coefficient of 12 and resembles an apparent 'all-or-none' phenomenon. The non-linearity seems to arise from InsP3 metabolism. However, it is not clear which InsP3-metabolising pathway engenders the non-linear behaviour nor whether ICRAC is always activated to its maximal extent by InsP3. 2. Using the whole-cell patch clamp technique, we dialysed RBL-1 cells with different concentrations of the InsP3 analogue InsP3-F. InsP3-F is broken down by Ins(1,4,5)P3 5-phosphatase but is not a substrate for Ins(1,4,5)P3 3-kinase. The relationship between InsP3-F and ICRAC amplitude was supra-linear and very similar to that with InsP3 but was distinct from the graded relationship seen with the non-metabolisable analogue Ins2,4,5P3. 3. In the presence of high intracellular Ca2+ buffer, InsP3-F activated ICRAC to its maximal extent. With moderate Ca2+ buffer, however, sub-maximal ICRAC could be obtained to a maximal InsP3-F concentration. Nevertheless, the relationship between the amplitude of ICRAC and InsP3-F concentration was still supra-linear. 4. Submaximal ICRAC in response to InsP3-F in the presence of moderate Ca2+ buffer was due to partial depletion of the stores, because the size of the current could be increased by thapsigargin. 5. The data suggest that first Ins(1,4,5)P3 5-phosphatase is an important factor which contributes to the non-linear relationship between InsP3 concentration and the amplitude of ICRAC and second, InsP3 does not always activate ICRAC to its maximal extent. At moderate buffer strengths, submaximal ICRAC is evoked by maximal InsP3. However, the supra-linear relationship between InsP3 concentration and amplitude of the current still holds.

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Year:  2000        PMID: 10699074      PMCID: PMC2269810          DOI: 10.1111/j.1469-7793.2000.t01-2-00283.x

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  24 in total

1.  On the characterisation of the mechanism underlying passive activation of the Ca2+ release-activated Ca2+ current ICRAC in rat basophilic leukaemia cells.

Authors:  L Fierro; A B Parekh
Journal:  J Physiol       Date:  1999-10-15       Impact factor: 5.182

Review 2.  Metabolism of inositol phosphates.

Authors:  S B Shears
Journal:  Adv Second Messenger Phosphoprotein Res       Date:  1992

3.  Substantial depletion of the intracellular Ca2+ stores is required for macroscopic activation of the Ca2+ release-activated Ca2+ current in rat basophilic leukaemia cells.

Authors:  L Fierro; A B Parekh
Journal:  J Physiol       Date:  2000-01-15       Impact factor: 5.182

Review 4.  Inositol trisphosphate and calcium signalling.

Authors:  M J Berridge
Journal:  Nature       Date:  1993-01-28       Impact factor: 49.962

5.  Thapsigargin, a tumor promoter, discharges intracellular Ca2+ stores by specific inhibition of the endoplasmic reticulum Ca2(+)-ATPase.

Authors:  O Thastrup; P J Cullen; B K Drøbak; M R Hanley; A P Dawson
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

6.  2,3-Diphosphoglycerate is a nonselective inhibitor of inositol 1,4,5-trisphosphate action and metabolism.

Authors:  G Guillemette; I Favreau; S Lamontagne; G Boulay
Journal:  Eur J Pharmacol       Date:  1990-04-25       Impact factor: 4.432

7.  Agonist-stimulated divalent cation entry into single cultured human umbilical vein endothelial cells.

Authors:  R Jacob
Journal:  J Physiol       Date:  1990-02       Impact factor: 5.182

8.  3-position modification of myo-inositol 1,4,5-trisphosphate: consequences for intracellular Ca2+ mobilisation and enzyme recognition.

Authors:  S T Safrany; R A Wilcox; C Liu; B V Potter; S R Nahorski
Journal:  Eur J Pharmacol       Date:  1992-07-01       Impact factor: 4.432

9.  Depletion of intracellular calcium stores activates a calcium current in mast cells.

Authors:  M Hoth; R Penner
Journal:  Nature       Date:  1992-01-23       Impact factor: 49.962

10.  Relationship between secretagogue-induced Ca2+ release and inositol polyphosphate production in permeabilized pancreatic acinar cells.

Authors:  H Streb; J P Heslop; R F Irvine; I Schulz; M J Berridge
Journal:  J Biol Chem       Date:  1985-06-25       Impact factor: 5.157

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  17 in total

1.  Respiring mitochondria determine the pattern of activation and inactivation of the store-operated Ca(2+) current I(CRAC).

Authors:  J A Gilabert; A B Parekh
Journal:  EMBO J       Date:  2000-12-01       Impact factor: 11.598

2.  Voltage-dependent conductance changes in the store-operated Ca2+ current ICRAC in rat basophilic leukaemia cells.

Authors:  D Bakowski; A B Parekh
Journal:  J Physiol       Date:  2000-12-01       Impact factor: 5.182

3.  Energized mitochondria increase the dynamic range over which inositol 1,4,5-trisphosphate activates store-operated calcium influx.

Authors:  J A Gilabert; D Bakowski; A B Parekh
Journal:  EMBO J       Date:  2001-06-01       Impact factor: 11.598

4.  Store-operated Ca2+ entry: dynamic interplay between endoplasmic reticulum, mitochondria and plasma membrane.

Authors:  Anant B Parekh
Journal:  J Physiol       Date:  2003-02-07       Impact factor: 5.182

5.  Intracellular Ca(2+) release via the ER translocon activates store-operated calcium entry.

Authors:  Hwei L Ong; Xibao Liu; Ajay Sharma; Ramanujan S Hegde; Indu S Ambudkar
Journal:  Pflugers Arch       Date:  2006-12-14       Impact factor: 3.657

6.  ATP depletion inhibits Ca2+ release, influx and extrusion in pancreatic acinar cells but not pathological Ca2+ responses induced by bile.

Authors:  Stephanie L Barrow; Svetlana G Voronina; Gabriela da Silva Xavier; Misha A Chvanov; Rebecca E Longbottom; Oleg V Gerasimenko; Ole H Petersen; Guy A Rutter; Alexei V Tepikin
Journal:  Pflugers Arch       Date:  2007-10-20       Impact factor: 3.657

7.  Store-operated Ca2+ entry depends on mitochondrial Ca2+ uptake.

Authors:  Maike D Glitsch; Daniel Bakowski; Anant B Parekh
Journal:  EMBO J       Date:  2002-12-16       Impact factor: 11.598

8.  Adenophostin A and ribophostin, but not inositol 1,4,5-trisphosphate or manno-adenophostin, activate the Ca2+ release-activated Ca2+ current, I(CRAC), in weak intracellular Ca2+ buffer.

Authors:  Anant B Parekh; Andrew M Riley; Barry V L Potter
Journal:  Biochem J       Date:  2002-01-01       Impact factor: 3.857

9.  Molecular clustering of STIM1 with Orai1/CRACM1 at the plasma membrane depends dynamically on depletion of Ca2+ stores and on electrostatic interactions.

Authors:  Nathaniel Calloway; Monika Vig; Jean-Pierre Kinet; David Holowka; Barbara Baird
Journal:  Mol Biol Cell       Date:  2008-11-05       Impact factor: 4.138

Review 10.  B-lymphocyte calcium influx.

Authors:  Leslie B King; Bruce D Freedman
Journal:  Immunol Rev       Date:  2009-09       Impact factor: 12.988

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