Literature DB >> 10781013

Apparent species differences in the kinetic properties of P2X(7) receptors.

A D Hibell1, E J Kidd, I P Chessell, P P Humphrey, A D Michel.   

Abstract

1. Apparent species differences in the responses of recombinant P2X(7) receptors to repeated application of 2'- and 3'-O-(4-benzoylbenzoyl)-ATP (BzATP) have been investigated. 2. Repeated application of 100 microM BzATP resulted in a progressive increase in current magnitude (current growth) at mouse and human, but not rat P2X(7) receptors. 3. Current growth was thought to reflect progressive dilation of the P2X(7) ion-channel to a pore permeable to large molecules (MW<900), suggesting that channel dilation was not occurring at the rat P2X(7) receptor. However, 100 microM BzATP produced a rapid influx of YO-PRO-1 (MW375) in cells expressing rat or human P2X(7) receptors. 4. There were, however, species differences in agonist potency such that 100 microM BzATP was a supra-maximal concentration at rat, but not human or mouse, P2X(7) receptors. Importantly, when sub-maximal concentrations of BzATP or ATP were examined, current growth occurred at rat P2X(7) receptors. 5. The rate of current growth and YO-PRO-1 accumulation increased with agonist concentration and appeared more rapid at rat and human, than at mouse P2X(7) receptors. 6. The potency of BzATP and ATP was 1.5 - 10 fold lower in naïve cells than in cells repeatedly exposed to ATP. 7. This study demonstrates that current growth occurs at mouse, rat and human P2X(7) receptors but only when using sub-maximal concentrations of agonist. Previously, current growth was thought to reflect the progressive increase in pore diameter of the P2X(7) receptor ion channel, however, the results of this study suggest a progressive increase in agonist potency may also contribute.

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Year:  2000        PMID: 10781013      PMCID: PMC1572049          DOI: 10.1038/sj.bjp.0703302

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  17 in total

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Journal:  Pflugers Arch       Date:  1981-08       Impact factor: 3.657

3.  Ionic effects on human recombinant P2X7 receptor function.

Authors:  A D Michel; I P Chessell; P P Humphrey
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1999-02       Impact factor: 3.000

4.  ATP-induced pore formation in the plasma membrane of rat peritoneal mast cells.

Authors:  P E Tatham; M Lindau
Journal:  J Gen Physiol       Date:  1990-03       Impact factor: 4.086

5.  A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine.

Authors:  E M Fenwick; A Marty; E Neher
Journal:  J Physiol       Date:  1982-10       Impact factor: 5.182

6.  Cloning and functional characterisation of the mouse P2X7 receptor.

Authors:  I P Chessell; J Simon; A D Hibell; A D Michel; E A Barnard; P P Humphrey
Journal:  FEBS Lett       Date:  1998-11-13       Impact factor: 4.124

7.  Isoquinolines as antagonists of the P2X7 nucleotide receptor: high selectivity for the human versus rat receptor homologues.

Authors:  B D Humphreys; C Virginio; A Surprenant; J Rice; G R Dubyak
Journal:  Mol Pharmacol       Date:  1998-07       Impact factor: 4.436

8.  Differential activation of cation channels and non-selective pores by macrophage P2z purinergic receptors expressed in Xenopus oocytes.

Authors:  L C Nuttle; G R Dubyak
Journal:  J Biol Chem       Date:  1994-05-13       Impact factor: 5.157

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10.  Upregulation of the enzyme chain hydrolyzing extracellular ATP after transient forebrain ischemia in the rat.

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  29 in total

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Review 2.  Molecular and functional properties of P2X receptors--recent progress and persisting challenges.

Authors:  Karina Kaczmarek-Hájek; Eva Lörinczi; Ralf Hausmann; Annette Nicke
Journal:  Purinergic Signal       Date:  2012-05-01       Impact factor: 3.765

3.  C-terminal calmodulin-binding motif differentially controls human and rat P2X7 receptor current facilitation.

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4.  Conserved ectodomain cysteines are essential for rat P2X7 receptor trafficking.

Authors:  Marie Jindrichova; Pavlo Kuzyk; Shuo Li; Stanko S Stojilkovic; Hana Zemkova
Journal:  Purinergic Signal       Date:  2012-06       Impact factor: 3.765

5.  Identification of Thr283 as a key determinant of P2X7 receptor function.

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Journal:  Br J Pharmacol       Date:  2006-08-29       Impact factor: 8.739

Review 6.  Pharmacology of P2X channels.

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Review 7.  Activation and regulation of purinergic P2X receptor channels.

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8.  Residues 155 and 348 contribute to the determination of P2X7 receptor function via distinct mechanisms revealed by single-nucleotide polymorphisms.

Authors:  Helen J Bradley; Jocelyn M Baldwin; G Ranjan Goli; Brian Johnson; Jie Zou; Asipu Sivaprasadarao; Stephen A Baldwin; Lin-Hua Jiang
Journal:  J Biol Chem       Date:  2011-01-04       Impact factor: 5.157

9.  P2X7 receptor activation regulates microglial cell death during oxygen-glucose deprivation.

Authors:  Ukpong B Eyo; Sam A Miner; Katelin E Ahlers; Long-Jun Wu; Michael E Dailey
Journal:  Neuropharmacology       Date:  2013-06-12       Impact factor: 5.250

10.  Functional interactions between P2X4 and P2X7 receptors from mouse salivary epithelia.

Authors:  Griselda Casas-Pruneda; Juan Pablo Reyes; Gabriela Pérez-Flores; Patricia Pérez-Cornejo; Jorge Arreola
Journal:  J Physiol       Date:  2009-04-29       Impact factor: 5.182

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