Regulation of TRPC6 Channel Activity by Tyrosine Phosphorylation*

Various hormonal stimuli and growth factors activate the mammalian canonical transient receptor potential (TRPC) channel through phospholipase C (PLC) activation. However, the precise mechanism of the regulation of TRPC channel activity remains unknown. Here, we provide the first evidence that direct tyrosine phosphorylation by Src family protein-tyrosine kinases (PTKs) is a novel mechanism for modulating TRPC6 channel activity. We found that TRPC6 is tyrosine-phosphorylated in COS-7 cells when coexpressed with Fyn, a member of the Src family PTKs. We also found that Fyn interacts with TRPC6 and that the interaction is mediated by the SH2 domain of Fyn and the N-terminal region of TRPC6 in a phosphorylation-independent manner. In addition, we demonstrated the physical association of TRPC6 with Fyn in the mammalian brain. Moreover, we showed that stimulation of the epidermal growth factor receptor induced rapid tyrosine phosphorylation of TRPC6 in COS-7 cells. This epidermal growth factor-induced tyrosine phosphorylation of TRPC6 was significantly blocked by PP2, a specific inhibitor of Src family PTKs, and by a dominant negative form of Fyn, suggesting that the direct phosphorylation of TRPC6 by Src family PTKs could be caused by physiological stimulation. Furthermore, using single channel recording, we showed that Fyn modulates TRPC6 channel activity via tyrosine phosphorylation. Thus, our findings demonstrated that tyrosine phosphorylation by Src family PTKs is a novel regulatory mechanism of TRPC6 channel activity.

[1]  E. Newell,et al.  Regulation of a TRPM7-like Current in Rat Brain Microglia* , 2003, Journal of Biological Chemistry.

[2]  Joseph P. Yuan,et al.  Homer Binds TRPC Family Channels and Is Required for Gating of TRPC1 by IP3 Receptors , 2003, Cell.

[3]  Brij B. Singh,et al.  Caveolin-1 Contributes to Assembly of Store-operated Ca2+ Influx Channels by Regulating Plasma Membrane Localization of TRPC1* , 2003, Journal of Biological Chemistry.

[4]  Kiyotsugu Yoshida,et al.  Regulation of a Transient Receptor Potential (TRP) Channel by Tyrosine Phosphorylation , 2003, The Journal of Biological Chemistry.

[5]  G. Schultz,et al.  Lanthanides Potentiate TRPC5 Currents by an Action at Extracellular Sites Close to the Pore Mouth* , 2003, The Journal of Biological Chemistry.

[6]  W. Schilling,et al.  Selective Association of TRPC Channel Subunits in Rat Brain Synaptosomes* 210 , 2002, The Journal of Biological Chemistry.

[7]  K. Venkatachalam,et al.  The cellular and molecular basis of store-operated calcium entry , 2002, Nature Cell Biology.

[8]  V. Flockerzi,et al.  Expression and role of TRPC proteins in human platelets: evidence that TRPC6 forms the store-independent calcium entry channel. , 2002, Blood.

[9]  G. Boulay Ca(2+)-calmodulin regulates receptor-operated Ca(2+) entry activity of TRPC6 in HEK-293 cells. , 2002, Cell calcium.

[10]  D. J. Brasier,et al.  cAMP-Dependent Protein Kinase Regulates Desensitization of the Capsaicin Receptor (VR1) by Direct Phosphorylation , 2002, Neuron.

[11]  C. Montell,et al.  The TRP Channels, a Remarkably Functional Family , 2002, Cell.

[12]  G. Schultz,et al.  TRPC6 is a candidate channel involved in receptor-stimulated cation currents in A7r5 smooth muscle cells. , 2002, American journal of physiology. Cell physiology.

[13]  Katsuhiko Mikoshiba,et al.  BANK regulates BCR‐induced calcium mobilization by promoting tyrosine phosphorylation of IP3 receptor , 2002, The EMBO journal.

[14]  F. Giancotti,et al.  EGF-R signaling through Fyn kinase disrupts the function of integrin α6β4 at hemidesmosomes , 2001, The Journal of cell biology.

[15]  M. Shibuya,et al.  Unique phosphorylation mechanism of Gab1 using PI 3-kinase as an adaptor protein. , 2001, Biochemical and biophysical research communications.

[16]  C. Montell Physiology, Phylogeny, and Functions of the TRP Superfamily of Cation Channels , 2001, Science's STKE.

[17]  D. Clapham,et al.  The trp ion channel family , 2001, Nature Reviews Neuroscience.

[18]  E. Stefani,et al.  Activation of Trp3 by inositol 1,4,5-trisphosphate receptors through displacement of inhibitory calmodulin from a common binding domain , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[19]  Y. Hara,et al.  The Transient Receptor Potential Protein Homologue TRP6 Is the Essential Component of Vascular &agr;1-Adrenoceptor–Activated Ca2+-Permeable Cation Channel , 2001, Circulation research.

[20]  A. Aromolaran,et al.  Agents that increase tyrosine phosphorylation activate a non‐selective cation current in single rabbit portal vein smooth muscle cells , 2001, The Journal of physiology.

[21]  L. Premkumar,et al.  Induction of vanilloid receptor channel activity by protein kinase C , 2000, Nature.

[22]  Yufang Tang,et al.  Association of Mammalian Trp4 and Phospholipase C Isozymes with a PDZ Domain-containing Protein, NHERF* , 2000, The Journal of Biological Chemistry.

[23]  C. Montell,et al.  TRP and the PDZ Protein, Inad, Form the Core Complex Required for Retention of the Signalplex in Drosophila Photoreceptor Cells , 2000, The Journal of cell biology.

[24]  S. Muallem,et al.  Gating of store-operated channels by conformational coupling to ryanodine receptors. , 2000, Molecular cell.

[25]  Brij B. Singh,et al.  Assembly of Trp1 in a Signaling Complex Associated with Caveolin-Scaffolding Lipid Raft Domains* , 2000, The Journal of Biological Chemistry.

[26]  K. Mikoshiba,et al.  Modulation of Ca(2+) entry by polypeptides of the inositol 1,4, 5-trisphosphate receptor (IP3R) that bind transient receptor potential (TRP): evidence for roles of TRP and IP3R in store depletion-activated Ca(2+) entry. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[27]  Y. Mori,et al.  Molecular and Functional Characterization of a Novel Mouse Transient Receptor Potential Protein Homologue TRP7 , 1999, The Journal of Biological Chemistry.

[28]  C. Montell,et al.  Activation of a TRPC3-Dependent Cation Current through the Neurotrophin BDNF , 1999, Neuron.

[29]  S. Muallem,et al.  The N-terminal domain of the IP3 receptor gates store-operated hTrp3 channels. , 1999, Molecular cell.

[30]  T. Gudermann,et al.  Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol , 1999, Nature.

[31]  S. Nakanishi,et al.  PSD-95 promotes Fyn-mediated tyrosine phosphorylation of the N-methyl-D-aspartate receptor subunit NR2A. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[32]  J. Putney,et al.  Capacitative calcium entry channels , 1999, BioEssays : news and reviews in molecular, cellular and developmental biology.

[33]  S. Muallem,et al.  Functional interaction between InsP3 receptors and store-operated Htrp3 channels , 1998, Nature.

[34]  M. Freichel,et al.  A novel capacitative calcium entry channel expressed in excitable cells , 1998, The EMBO journal.

[35]  R. Hurst,et al.  Cloning and Expression of a Novel Mammalian Homolog ofDrosophila Transient Receptor Potential (Trp) Involved in Calcium Entry Secondary to Activation of Receptors Coupled by the Gq Class of G Protein* , 1997, The Journal of Biological Chemistry.

[36]  R. Penner,et al.  Store depletion and calcium influx. , 1997, Physiological reviews.

[37]  T. Takenawa,et al.  β-Tubulin Binds Src Homology 2 Domains through a Region Different from the Tyrosine-phosphorylated Protein-recognizing Site* , 1996, The Journal of Biological Chemistry.

[38]  G. Schultz,et al.  Cloning and Functional Expression of a Human Ca2+-Permeable Cation Channel Activated by Calcium Store Depletion , 1996, Neuron.

[39]  R. Hurst,et al.  trp, a Novel Mammalian Gene Family Essential for Agonist-Activated Capacitative Ca2+ Entry , 1996, Cell.

[40]  S. Matsuda,et al.  Physical and functional interactions of protein tyrosine kinases, p59fyn and ZAP-70, in T cell signaling. , 1996, Journal of immunology.

[41]  D. Morrison,et al.  Raf-1 interacts with Fyn and Src in a non-phosphotyrosine-dependent manner. , 1994, The Journal of biological chemistry.

[42]  Yu Tian Wang,et al.  Regulation of NMDA receptors by tyrosine kinases and phosphatases , 1994, Nature.

[43]  Xin-Yun Huang,et al.  Tyrosine kinase-dependent suppression of a potassium channel by the G protein-coupled m1 muscarinic acetylcholine receptor , 1993, Cell.