Literature DB >> 15525684

Polarized expression of human P2Y receptors in epithelial cells from kidney, lung, and colon.

Samuel C Wolff1, Ai-Dong Qi, T Kendall Harden, Robert A Nicholas.   

Abstract

Eight human G protein-coupled P2Y receptors (P2Y(1), P2Y(2), P2Y(4), P2Y(6), P2Y(11), P2Y(12), P2Y(13), and P2Y(14)) that respond to extracellular nucleotides have been molecularly identified and characterized. P2Y receptors are widely expressed in epithelial cells and play an important role in regulating epithelial cell function. Functional studies assessing the capacity of various nucleotides to promote increases in short-circuit current (I(sc)) or Ca(2+) mobilization have suggested that some subtypes of P2Y receptors are polarized with respect to their functional activity, although these results often have been contradictory. To investigate the polarized expression of the family of P2Y receptors, we determined the localization of the entire P2Y family after expression in Madin-Darby canine kidney (MDCK) type II cells. Confocal microscopy of polarized monolayers revealed that P2Y(1), P2Y(11), P2Y(12), and P2Y(14) receptors reside at the basolateral membrane, P2Y(2), P2Y(4), and P2Y(6) receptors are expressed at the apical membrane, and the P2Y(13) receptor is unsorted. Biotinylation studies and I(sc) measurements in response to the appropriate agonists were consistent with the polarized expression observed in confocal microscopy. Expression of the G(q)-coupled P2Y receptors (P2Y(1), P2Y(2), P2Y(4), P2Y(6), and P2Y(11)) in lung and colonic epithelial cells (16HBE14o- and Caco-2 cells, respectively) revealed a targeting profile nearly identical to that observed in MDCK cells, suggesting that polarized targeting of these P2Y receptor subtypes is not a function of the type of epithelial cell in which they are expressed. These experiments highlight the highly polarized expression of P2Y receptors in epithelial cells.

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Year:  2004        PMID: 15525684     DOI: 10.1152/ajpcell.00338.2004

Source DB:  PubMed          Journal:  Am J Physiol Cell Physiol        ISSN: 0363-6143            Impact factor:   4.249


  16 in total

1.  Charged residues in the C-terminus of the P2Y1 receptor constitute a basolateral-sorting signal.

Authors:  Samuel C Wolff; Ai-Dong Qi; T Kendall Harden; Robert A Nicholas
Journal:  J Cell Sci       Date:  2010-07-15       Impact factor: 5.285

2.  The transforming Rho family GTPase Wrch-1 disrupts epithelial cell tight junctions and epithelial morphogenesis.

Authors:  Donita C Brady; Jamie K Alan; James P Madigan; Alan S Fanning; Adrienne D Cox
Journal:  Mol Cell Biol       Date:  2008-12-08       Impact factor: 4.272

3.  Purinergic inhibition of Na⁺,K⁺,Cl⁻ cotransport in C11-MDCK cells: Role of stress-activated protein kinases.

Authors:  Olga A Akimova; Sebastien Taurin; Nickolai O Dulin; Sergei N Orlov
Journal:  Purinergic Signal       Date:  2007-06-30       Impact factor: 3.765

4.  Apical targeting of the P2Y(4) receptor is directed by hydrophobic and basic residues in the cytoplasmic tail.

Authors:  D Ross DuBose; Samuel C Wolff; Ai-Dong Qi; Izabela Naruszewicz; Robert A Nicholas
Journal:  Am J Physiol Cell Physiol       Date:  2012-10-10       Impact factor: 4.249

Review 5.  A critical look at the function of the P2Y11 receptor.

Authors:  Karin Dreisig; Birgitte Rahbek Kornum
Journal:  Purinergic Signal       Date:  2016-05-31       Impact factor: 3.765

6.  Adenosine-evoked Na+ transport in human airway epithelial cells.

Authors:  L A Chambers; M Constable; M T Clunes; R E Olver; W H Ko; S K Inglis; S M Wilson
Journal:  Br J Pharmacol       Date:  2006-07-31       Impact factor: 8.739

7.  The role of epithelial P2Y2 and P2Y4 receptors in the regulation of intestinal chloride secretion.

Authors:  Esam Ghanem; Bernard Robaye; Teresinha Leal; Jens Leipziger; Willy Van Driessche; Renaud Beauwens; Jean-Marie Boeynaems
Journal:  Br J Pharmacol       Date:  2005-10       Impact factor: 8.739

8.  The inhibitory role of purinergic P2Y receptor on Mg2+ transport across intestinal epithelium-like Caco-2 monolayer.

Authors:  Narongrit Thongon; Siriporn Chamniansawat
Journal:  J Physiol Sci       Date:  2018-07-21       Impact factor: 2.781

9.  Cl- secretion in ATP-treated renal epithelial C7-MDCK cells is mediated by activation of P 2Y1 receptors, phospholipase A2 and protein kinase A.

Authors:  A Olga Akimova; Nathalie Bourcier; Sebastien Taurin; Richard A Bundey; Konrad Grygorczyk; Michael Gekle; Paul A Insel; Nickolai O Dulin; Sergei N Orlov
Journal:  J Physiol       Date:  2005-08-18       Impact factor: 5.182

10.  Quantification of Gi-mediated inhibition of adenylyl cyclase activity reveals that UDP is a potent agonist of the human P2Y14 receptor.

Authors:  Rhonda L Carter; Ingrid P Fricks; Matthew O Barrett; Lauren E Burianek; Yixing Zhou; Hyojin Ko; Arijit Das; Kenneth A Jacobson; Eduardo R Lazarowski; T Kendall Harden
Journal:  Mol Pharmacol       Date:  2009-09-16       Impact factor: 4.436

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