Differential roles of NHERF1, NHERF2, and PDZK1 in regulating CFTR-mediated intestinal anion secretion in mice.

The epithelial anion channel CFTR interacts with multiple PDZ domain-containing proteins. Heterologous expression studies have demonstrated that the Na+/H+ exchanger regulatory factors, NHERF1, NHERF2, and PDZK1 (NHERF3), modulate CFTR membrane retention, conductivity, and interactions with other transporters. To study their biological roles in vivo, we investigated CFTR-dependent duodenal HCO3- secretion in mouse models of Nherf1, Nherf2, and Pdzk1 loss of function. We found that Nherf1 ablation strongly reduced basal as well as forskolin-stimulated (FSK-stimulated) HCO3- secretory rates and blocked beta2-adrenergic receptor (beta2-AR) stimulation. Conversely, Nherf2-/- mice displayed augmented FSK-stimulated HCO3- secretion. Furthermore, although lysophosphatidic acid (LPA) inhibited FSK-stimulated HCO3- secretion in WT mice, this effect was lost in Nherf2-/- mice. Pdzk1 ablation reduced basal, but not FSK-stimulated, HCO3- secretion. In addition, laser microdissection and quantitative PCR revealed that the beta2-AR and the type 2 LPA receptor were expressed together with CFTR in duodenal crypts and that colocalization of the beta2-AR and CFTR was reduced in the Nherf1-/- mice. These data suggest that the NHERF proteins differentially modulate duodenal HCO3- secretion: while NHERF1 is an obligatory linker for beta2-AR stimulation of CFTR, NHERF2 confers inhibitory signals by coupling the LPA receptor to CFTR.

[1]  M. Donowitz,et al.  Defective jejunal and colonic salt absorption and alteredNa+/H+ exchanger 3 (NHE3) activity in NHE regulatory factor 1 (NHERF1) adaptor protein-deficient mice , 2009, Pflügers Archiv - European Journal of Physiology.

[2]  Jin-Xia Zhu,et al.  β-Adrenoceptors, but not dopamine receptors, mediate dopamine-induced ion transport in late distal colon of rats , 2008, Cell and Tissue Research.

[3]  M. Manns,et al.  CFTR and its key role in in vivo resting and luminal acid‐induced duodenal HCO3− secretion , 2008, Acta physiologica.

[4]  Ding-zhen Luo,et al.  Alteration of dopaminergic markers in gastrointestinal tract of different rodent models of Parkinson's disease , 2008, Neuroscience.

[5]  S. Shenolikar,et al.  Cystic Fibrosis Transmembrane Conductance Regulator Activation Is Reduced in the Small Intestine of Na+/H+ Exchanger 3 Regulatory Factor 1 (NHERF-1)- but Not NHERF-2-deficient Mice* , 2007, Journal of Biological Chemistry.

[6]  M. Zaccolo,et al.  Spatiotemporal Coupling of cAMP Transporter to CFTR Chloride Channel Function in the Gut Epithelia , 2007, Cell.

[7]  M. Manns,et al.  Sodium and chloride absorptive defects in the small intestine in Slc26a6 null mice , 2007, Pflügers Archiv - European Journal of Physiology.

[8]  M. Manns,et al.  NHE3 inhibition by cAMP and Ca2+ is abolished in PDZ‐domain protein PDZK1‐deficient murine enterocytes , 2007, The Journal of physiology.

[9]  Aleksandr Kivenson,et al.  Targeting CAL as a negative regulator of DeltaF508-CFTR cell-surface expression: an RNA interference and structure-based mutagenetic approach. , 2007, The Journal of biological chemistry.

[10]  M. Manns,et al.  Down regulation of small intestinal ion transport in PDZK1- (CAP70/NHERF3) deficient mice , 2007, Pflügers Archiv - European Journal of Physiology.

[11]  U. Seidler,et al.  The emerging role of PDZ adapter proteins for regulation of intestinal ion transport. , 2006, American journal of physiology. Gastrointestinal and liver physiology.

[12]  P. Suh,et al.  NHE3 inhibits PKA-dependent functional expression of CFTR by NHERF2 PDZ interactions. , 2006, Biochemical and biophysical research communications.

[13]  Paul W Wiseman,et al.  Membrane lateral diffusion and capture of CFTR within transient confinement zones. , 2006, Biophysical journal.

[14]  W. Guggino,et al.  New insights into cystic fibrosis: molecular switches that regulate CFTR , 2006, Nature reviews. Molecular cell biology.

[15]  M. Conese,et al.  Na+/H+ Exchanger Regulatory Factor Isoform 1 Overexpression Modulates Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Expression and Activity in Human Airway 16HBE14o- Cells and Rescues ΔF508 CFTR Functional Expression in Cystic Fibrosis Cells* , 2005, Journal of Biological Chemistry.

[16]  D. Callaway,et al.  Ezrin Controls the Macromolecular Complexes Formed between an Adapter Protein Na+/H+ Exchanger Regulatory Factor and the Cystic Fibrosis Transmembrane Conductance Regulator* , 2005, Journal of Biological Chemistry.

[17]  A. Naren,et al.  Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners. , 2005, Pharmacology & therapeutics.

[18]  Y. Fujiwara,et al.  Lysophosphatidic acid inhibits cholera toxin-induced secretory diarrhea through CFTR-dependent protein interactions , 2005, The Journal of experimental medicine.

[19]  P. Aronson,et al.  Role of PDZK1 in membrane expression of renal brush border ion exchangers. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[20]  E. Lakatta,et al.  Heterodimerization of β1- and β2-Adrenergic Receptor Subtypes Optimizes β-Adrenergic Modulation of Cardiac Contractility , 2005 .

[21]  W. Thelin,et al.  Beyond the brush border: NHERF4 blazes new NHERF turf , 2005, The Journal of physiology.

[22]  N. Déliot,et al.  NaPi‐IIa and interacting partners , 2005, The Journal of physiology.

[23]  M. Donowitz,et al.  NHERF family and NHE3 regulation , 2005, The Journal of physiology.

[24]  K. Lackner,et al.  The CFTR associated protein CAP70 interacts with the apical Cl-/HCO3- exchanger DRA in rabbit small intestinal mucosa. , 2005, Biochemistry.

[25]  C. Beglinger,et al.  MAPPING OF MULTIDRUG RESISTANCE GENE 1 AND MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN ISOFORM 1 TO 5 mRNA EXPRESSION ALONG THE HUMAN INTESTINAL TRACT , 2005, Drug Metabolism and Disposition.

[26]  K. Dev,et al.  Making protein interactions druggable: targeting PDZ domains , 2004, Nature Reviews Drug Discovery.

[27]  A. Naren,et al.  Molecular Assembly of Cystic Fibrosis Transmembrane Conductance Regulator in Plasma Membrane* , 2004, Journal of Biological Chemistry.

[28]  S. Muallem,et al.  Gating of CFTR by the STAS domain of SLC26 transporters , 2004, Nature Cell Biology.

[29]  A. Verkman,et al.  Increased Diffusional Mobility of CFTR at the Plasma Membrane after Deletion of Its C-terminal PDZ Binding Motif* , 2004, Journal of Biological Chemistry.

[30]  S. Shenolikar,et al.  Localization and interaction of NHERF isoforms in the renal proximal tubule of the mouse. , 2003, American journal of physiology. Cell physiology.

[31]  S. Grinstein,et al.  The Role of the C Terminus and Na+/H+ Exchanger Regulatory Factor in the Functional Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Nonpolarized Cells and Epithelia* , 2003, Journal of Biological Chemistry.

[32]  A. Gilchrist,et al.  Targeted Disruption of the PDZK1 Gene by Homologous Recombination , 2003, Molecular and Cellular Biology.

[33]  J. Clancy,et al.  A macromolecular complex of β2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKA , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[34]  G. Cutting,et al.  PDZ Domain Interaction Controls the Endocytic Recycling of the Cystic Fibrosis Transmembrane Conductance Regulator* , 2002, The Journal of Biological Chemistry.

[35]  M. Gregor,et al.  The down regulated in adenoma (dra) gene product binds to the second PDZ domain of the NHE3 kinase A regulatory protein (E3KARP), potentially linking intestinal Cl-/HCO3- exchange to Na+/H+ exchange. , 2002, Biochemistry.

[36]  S. Shenolikar,et al.  Targeted disruption of the mouse NHERF-1 gene promotes internalization of proximal tubule sodium-phosphate cotransporter type IIa and renal phosphate wasting , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[37]  A. Bagorda,et al.  Reciprocal Protein Kinase A Regulatory Interactions between Cystic Fibrosis Transmembrane Conductance Regulator and Na+/H+ Exchanger Isoform 3 in a Renal Polarized Epithelial Cell Model* , 2002, The Journal of Biological Chemistry.

[38]  D. Mak,et al.  Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[39]  W. Guggino,et al.  Accessory Protein Facilitated CFTR-CFTR Interaction, a Molecular Mechanism to Potentiate the Chloride Channel Activity , 2000, Cell.

[40]  N. Bradbury,et al.  E3KARP Mediates the Association of Ezrin and Protein Kinase A with the Cystic Fibrosis Transmembrane Conductance Regulator in Airway Cells* , 2000, The Journal of Biological Chemistry.

[41]  G. Cutting,et al.  The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane. , 2000, The Journal of biological chemistry.

[42]  I. Braakman,et al.  Regulated trafficking of the CFTR chloride channel. , 2000, European journal of cell biology.

[43]  B A Stanton,et al.  A PDZ-interacting domain in CFTR is an apical membrane polarization signal. , 1999, The Journal of clinical investigation.

[44]  S. Shenolikar,et al.  Assembly of signaling complexes by the sodium-hydrogen exchanger regulatory factor family of PDZ-containing proteins. , 1999, Current opinion in nephrology and hypertension.

[45]  W. Clauss,et al.  Minor Role of Cl– Secretion in Non-Cystic Fibrosis and Cystic Fibrosis Human Nasal Epithelium , 1999, Cellular Physiology and Biochemistry.

[46]  S. Beck,et al.  Lack of correlation between CFTR expression, CFTR Cl− currents, amiloride‐sensitive Na+ conductance, and cystic fibrosis phenotype , 1999, Pediatric pulmonology.

[47]  E. Weinman,et al.  The Role of NHERF and E3KARP in the cAMP-mediated Inhibition of NHE3* , 1998, The Journal of Biological Chemistry.

[48]  Agnieszka Sidor,et al.  NHE3 Kinase A Regulatory Protein E3KARP Binds the Epithelial Brush Border Na+/H+ Exchanger NHE3 and the Cytoskeletal Protein Ezrin* , 1998, The Journal of Biological Chemistry.

[49]  M. Welsh,et al.  A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[50]  M. Knowles,et al.  Effects of topically delivered benzamil and amiloride on nasal potential difference in cystic fibrosis. , 1998, American journal of respiratory and critical care medicine.

[51]  A. Bakker,et al.  Effect of clenbuterol on sarcoplasmic reticulum function in single skinned mammalian skeletal muscle fibers. , 1998, American journal of physiology. Cell physiology.

[52]  H. Rossmann,et al.  A functional CFTR protein is required for mouse intestinal cAMP‐, cGMP‐ and Ca2+‐dependent HCO3− secretion , 1997, The Journal of physiology.

[53]  J. Isenberg,et al.  Acid-stimulated duodenal bicarbonate secretion involves a CFTR-mediated transport pathway in mice. , 1997, Gastroenterology.

[54]  J. Isenberg,et al.  CFTR mediates cAMP- and Ca2+-activated duodenal epithelial HCO3- secretion. , 1997, The American journal of physiology.

[55]  M. Knowles,et al.  In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis. , 1995, Human gene therapy.

[56]  G. Flemström,et al.  Stimulation of mucosal alkaline secretion in rat duodenum by dopamine and dopaminergic compounds. , 1993, Gastroenterology.

[57]  S. Szabó,et al.  Dopamine in gastrointestinal disease , 1990, Digestive Diseases and Sciences.

[58]  E. Lakatta,et al.  Heterodimerization of beta1- and beta2-adrenergic receptor subtypes optimizes beta-adrenergic modulation of cardiac contractility. , 2005, Circulation research.

[59]  W. Guggino The cystic fibrosis transmembrane regulator forms macromolecular complexes with PDZ domain scaffold proteins. , 2004, Proceedings of the American Thoracic Society.

[60]  S. Shenolikar,et al.  Differential renal distribution of NHERF isoforms and their colocalization with NHE3, ezrin, and ROMK. , 2001, American journal of physiology. Cell physiology.

[61]  N. Ameen,et al.  Cellular localization of the cystic fibrosis transmembrane conductance regulator in mouse intestinal tract , 2000, Histochemistry and Cell Biology.

[62]  F. Collins,et al.  Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization. , 1994, The Journal of clinical investigation.