Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
6. References
C.M. Liedtke, T. Cole, and M. Ikebe, Differential activation of PKC-δ and PKC-ζ by α1-adrenergic stimulation in human airway epithelial cells, Am. J. Physiol. Cell Physiol. 273, C937–C943 (1997).
C.M. Liedtke and T. Cole, Antisense oligodeoxynucleotide to PKCδ blocks 1-adrenergic activation of Na-K-2Cl cotransport, Am. J. Physiol. Cell Physiol. 273, C1632–C1640 (1997).
Y. Jia, C.J. Mathews, and J.W. Hanrahan, Phosphorylation by protein kinase C is required for acute activation of cystic fibrosis transmembrane conductance regulator by protein kinase A, J. Biol. Chem. 272, 4978–4984 (1997).
L.M. Middleton and R.D. Harvey, PKC regulation of cardiac CFTR Cl− channel function in guinea pig ventricular myocytes, Am. J. Physiol. Cell Physiol. 275, C293–C302 (1998).
C.M. Liedtke and T. Cole, Antisense oligodeoxynucleotide to PKC-ε alters cAMP-dependent stimulation of CFTR in Calu-3 cells, Am. J. Physiol. Cell Physiol. 275:C1357–C1364 (1998).
R.V. Schillace and J.D. Scott, Organization of kinases, phosphatases, and receptor signaling complexes, J. Clin. Invest. 103, 761–765 (1999).
S. Jaken and P.J. Parker, Protein kinase C binding partners, BioEssays 22, 245–254 (2000).
D. Mochly-Rosen and A.S. Gordon, Anchoring proteins for protein kinase C: a means for isozyme selectivity, FASEB J. 12, 35–42 (1998).
C.M. Liedtke, D. Cody, and T.S. Cole, Differential regulation of Cl transport proteins by PKC in Calu-3 cells, Am. J. Physiol. Lung Cell. Molec. Physiol., 280, L739–L747 (2001).
C.M. Liedtke, R. Papay, and T.S. Cole, Modulation of Na/K/2Cl cotransport by intracellular Cl and protein kinase C-δ in Calu-3 cells, Am. J. Physiol Lung Cell. Mole. Physiol. 282, L1151–L1159 (2002).
C.M. Liedtke, C.H.C. Yun, N. Kyle, and D. Wang, PKC-δ dependent regulation of CFTR involves binding to RACK1, a Receptor for Activated C Kinase, and RACK1 binding to NHERF, J. Biol. Chem. 277, 22925–22933 (2002).
C.M. Liedtke, M. Hubbard, and X. Wang, Stability of actin cytoskeleton and PKC-δ binding to actin regulate NKCC1 function in airway epithelial cells, Am. J. Physiol. Cell. Physiol. 284, C487–C496 (2003).
L.C. D’Andrea, C. Lytle, J.B. Matthews, P. Hofman, B. Forbush III, and J.L. Madara, Na/K/2Cl cotransporter protein of intestinal epithelial cells: surface distribution, immunoprecipitation as a protein complex and surface expression in response to cAMP, J. Bio.l Chem. 271, 28969–28976 (1996).
J.B. Matthews, J.A. Smith, and B.J. Hrnjez, Effects of F-actin stabilization or disassembly on epithelial Cl− secretion and Na-K-2Cl cotransport, Am. J. Physiol. Cell Physiol. 272, C254–C262 (1997).
J.B. Matthews, J.A. Smith, E.C. Mun, and J.K. Sicklick, Osmotic regulation of intestinal epithelial Na-KCl cotransport: role of Cl and F-actin, Am. J. Physiol. Cell. Physiol. 274, C697–C706 (1998).
J.C. Song, B.J. Hrnjez, O.C. Farokhzad, and J.B. Matthews, PKC-ε regulates basolateral endocytosis in human intesinal epithelia: role of F-actin and MARCKS, Am. J. Physiol. Cell Physiol. 277, C1239–C1249 (1999).
I. Spector, F. Braet, N.R. Shochet, and M.R. Bubb, New anti-actin drugs in the study of the organization and function of the actin cytoskeleton, Microscopy Res. Technique 47, 18–37 (1999).
J.A. Johnson, M.O. Gray, H.-H. Chen, and D. Mochly-Rosen. A protein kinase C translocation inhibitor as an isozyme-selective antagonist of cardiac function, J. Biol. Chem. 271, 24962–24966 (1996).
G. Lopez-Lluch, M.M. Bird, B. Canas, J. Godovac-Zimmerman, A. Ridley, A.W. Segala and L.V. Dekker, Protein kinase C-δ C2-like domain is a binding site for actin and enables actin redistribution in neutrophils, Biochem. J. 357, 39–57 (2001).
D. Ron, C.H. Chen, J. Caldwell, L. Jamieson, E. Orr, and D. Mochly-Rosen, Cloning of the intracellular receptor for protein kinase C: a homolog of the β subunits of G proteins, Proc. Natl. Acad. Sci. USA 91, 839–843 (1994).
M. Csukai, C.-H. Chen, M.A. De Matteis, and D. Mochly-Rosen, The coatomer protein β-COP, a selective binding protein (RACK) for protein kinase Cε J. Biol. Chem. 272, 29200–29206 (1997).
D.B. Short, K.W. Trotter, D. Reczek, S.M. Kreda, A. Bretscher, R.C. Boucher, M.J. Stutts, and S.L. Milgram, An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton, J. Biol. Chem. 273,19797–19801 (1998).
S.S. Wang, R.W. Raab, W.B. Guggino, and M. Li, FEBS Lett. Peptide binding consensus of the NHE-RFPDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR), FEBS Lett. 427, 103–108 (1998)
V. Raghuram, D.-O.D. Mak, and J.K. Foskett, Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction. Proc. Natl. Acad. Sci. USA 98,1300–1305 (2001).
R.A. Hall, L.S. Ostedgaard, R.T. Premont, J.T. Blitzer, N. Rahman, M.J. Welsh, and R.J. Lefkowitz, A C-terminal motif found in the β2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins, Proc. Natl. Acad. Sci. USA 95, 8496–8501 (1998).
W. Ahn, K.H. Kim, J.A. Lee, J.Y. Kim, J.Y. Choi, O.W. Moe, S.L. Milgram, S. Muallem, and M.G. Lee, Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and CHO3-salvage mechanisms in model systems and the mouse pancreatic duct, J. Biol. Chem. 276, 17236–17243 (2001).
K. Kunzelmann, G.L. Kiser, R. Schreiber, and J.R. Riordan, Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator, FEBS Lett. 400, 341–344 (1997).
B.D. Moyer, J. Denton, K.H. Karlson, G.R. Reynolds, W.B. Guggino, M. Li, and B.A. Stanton, A PDZ-interacting domain in CFTR is an apical membrane polarization signal, J. Clin. Invest. 104, 1353–1361 (1999).
D. Reczer, M. Berryman, and A. Bretscher, Identification of EBP50: a PDZ-containing phosphoprotein that associates with members of the ERM family. J. Cell Biol. 139, 169–179 (1997).
L.V. Dekker and P.J. Parker, Regulated binding of the protein kinase C substrate GAP-43 to the V0/C2 region of protein kinase C-δ, J. Biol. Chem. 272, 12747–12753, (1997).
C. Keenan and D. Kelleher, Protein kinase C and the cytoskeleton, Cell Signal. 10:225–232 (1998).
B. Chasan, N.A. Geisse, K. Pedatella, D.G. Wooster, M. Teintze, M.D. Carattino, W.H. Goldmann, and H.F. Cantiello, Evidence for direct interaction between actin and the cystic fibrosis transmembrane conductance regulator, Eur. Biophys. J. 30, 617–624 (2002).
R. Prekeris, M.W. Mayhew, J.B. Cooper, and D.M. Terrian, Identification and localization of an actinbinding motif that is unique to the epsilon isoform of protein kinase C and participates in the regulation of synaptic function, J. Cell Biol. 132, 77–90 (1996).
J.C. Song, B.J. Hrnjez, O.C. Farokhzad, and J.B. Matthews, PKC-ε regulates basolateral endocytosis in human intestinal epithelia: Role of F-actin and MARCKS, Am. J. Physiol. Cell Physiol. 277, C1239–C1249, (1999).
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2004 Springer Science+Business Media, Inc.
About this paper
Cite this paper
Liedtke, C.M. (2004). Regulation of Epithelial Electrolyte Transporters through Protein-Protein Interactions. In: Lauf, P.K., Adragna, N.C. (eds) Cell Volume and Signaling. Advances in Experimental Medicine and Biology, vol 559. Springer, Boston, MA . https://doi.org/10.1007/0-387-23752-6_32
Download citation
DOI: https://doi.org/10.1007/0-387-23752-6_32
Publisher Name: Springer, Boston, MA
Print ISBN: 978-0-387-23299-7
Online ISBN: 978-0-387-23752-7
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)