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Proteomic analysis of TRPC5- and TRPC6-binding partners reveals interaction with the plasmalemmal Na+/K+-ATPase

  • Ion Channels, Transporters
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Abstract

Mammalian transient receptor potential canonical (TRPC) genes encode a family of nonselective cation channels that are activated following stimulation of G-protein-coupled membrane receptors linked to phospholipase C. In Drosophila photoreceptor cells, TRP channels are found in large, multimolecular signaling complexes in association with the PDZ-containing scaffolding protein, INAD. A similar mammalian TRPC “signalplex” has been proposed, but has yet to be defined. In the present study, affinity-purified polyclonal antibodies against TRPC5 and TRPC6 were used to immunoprecipitate signalplex components from rat brain lysates. Immunoprecipitated proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, digested with trypsin, and sequenced by mass spectrometry. Proteins identified in the immunoprecipitates included cytoskeletal proteins spectrin, myosin, actin, drebrin, tubulin, and neurabin; endocytic vesicle-associated proteins clathrin, dynamin and AP-2; and the plasmalemmal Na+/K+-ATPase (NKA) pump. Several of these interactions were confirmed by reciprocal immunoprecipitation followed by Western blot analysis. In lysates from rat kidney, TRPC6, but not TRPC3, was found to coimmunoprecipitate with the NKA pump. Likewise, TRPC6, stably expressed in human embryonic kidney (HEK) cells, coimmunoprecipitated with endogenous NKA and colocalized with the pump to the plasmalemma when examined by immunofluorescence microscopy. Cell surface biotinylation experiments in intact HEK cells, confirmed that both the Na+ pump and TRPC6 were present in the surface membrane and appeared to interact. Lastly, TRPC6 coimmunoprecipitated with the NKA pump when the proteins were coexpressed in Spodoptera frugiperda insect cells using recombinant baculoviruses. These observations suggest that TRPC6 and the Na+ pump are part of a functional complex that may be involved in ion transport and homeostasis in both the brain and kidney.

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References

  1. Aebersold R, Mann M (2003) Mass spectrometry-based proteomics. Nature 422:198–207

    Google Scholar 

  2. Allen PB, Ouimet CC, Greengard P (1997) Spinophilin, a novel protein phosphatase 1 binding protein localized to dendritic spines. Proc Natl Acad Sci USA 94:9956–9961

    Google Scholar 

  3. Bandyopadhyay BC, Swaim WD, Liu X, Redman R, Patterson RL, Ambudkar IS (2005) Apical localization of a functional TRPC3/TRPC6-Ca2+-signaling complex in polarized epithelial cells: role in apical Ca2+ influx. J Biol Chem 280:12908–12916

    Google Scholar 

  4. Delmas P, Wanaverbecq N, Abogadie FC, Mistry M, Brown DA (2002) Signaling microdomains define the specificity of receptor-mediated InsP3 pathways in neurons. Neuron 34:209–220

    Google Scholar 

  5. Estacion M, Li S, Sinkins WG, Gosling M, Bahra P, Poll C, Westwick J, Schilling WP (2004) Activation of human TRPC6 channels by receptor stimulation. J Biol Chem 279:22047–22056

    Google Scholar 

  6. Goel M, Sinkins WG, Schilling WP (2002) Selective association of TRPC channel subunits in rat brain synaptosomes. J Biol Chem 277:48303–48310

    Google Scholar 

  7. Hering H, Sheng M (2001) Dendritic spines: structure, dynamics and regulation. Nature Neurosci 2:880–888

    Google Scholar 

  8. Husi H, Grant SG (2001) Proteomics of the nervous system. Trends Neurosci 24:259–266

    Google Scholar 

  9. Husi H, Ward MA, Choudhary JS, Blackstock WP, Grant SG (2000) Proteomic analysis of NMDA receptor-adhesion protein signaling complexes. Nat Neurosci 3:661–669

    Google Scholar 

  10. Lockwich TP, Liu X, Singh BB, Jadlowiec J, Weiland S, Ambudkar IS (2000) Assembly of Trp1 in a signaling complex associated with caveolin-scaffolding lipid raft domains. J Biol Chem 275:11934–11942

    Google Scholar 

  11. Marks MS, Ohno H, Kirchhausen T, Bonifacino J (1997) Protein sorting by tyrosine-based signals: adapting to the Ys and wherefores. Trends Cell Biol 7:124–128

    Google Scholar 

  12. Monk PD, Carne A, Liu SH, Ford JW, Keen JN, Findlay JBC (1996) Isolation, cloning, and characterisation of a trp homologue from squid (Loligo forbesi) photoreceptor membranes. J Neurochem 67:2227–2235

    Google Scholar 

  13. Montell C (2005) The TRP superfamily of cation channels. Sci STKE.DOI DOI: 10.1126/stke.2722005re3.

  14. O’Reilly DR, Miller LK, Luckow VA (1992) Baculovirus expression vectors: a laboratory manual. Freeman, Salt Lake City

    Google Scholar 

  15. Putney JWJ (2004) The enigmatic TRPCs: multifunctional cation channels. Trends Cell Biol 14:282–286

    Google Scholar 

  16. Robinson M (1997) Coats and vesicle budding. Trends Cell Biol 7:99–102

    Google Scholar 

  17. Rose C, Konnerth A (2001) NMDA receptor-mediated Na+ signals in spines and dendrites. J Neurosci 21:4207–4214

    Google Scholar 

  18. Shirao T, Sekino Y (2001) Clustering and anchoring mechanisms of molecular constituents of post-synaptic scaffolds in dendritic spines. Neurosci Res 40:1–7

    Google Scholar 

  19. Tyers M, Mann M (2003) From genomics to proteomics. Nature 422:193–197

    Google Scholar 

  20. Wisnoskey BJ, Sinkins WG, Schilling WP (2003) Activation of vanilloid receptor type 1 in the endoplasmic reticulum fails to activate store-operated Ca2+ entry. Biochem J 372:517–528

    Google Scholar 

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Acknowledgement

This work was supported by NIH grant GM52019.

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Authors and Affiliations

  1. Rammelkamp Center for Education and Research Room R-322, MetroHealth Medical Center, 2500 MetroHealth Drive, Cleveland, OH, 44109-1998, USA

    William P. Schilling

  2. Department of Cell Biology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, 44106, USA

    Andrew Keightley & Michael Kinter

  3. Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA

    Monu Goel, William Sinkins & William P. Schilling

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  1. Monu Goel
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  2. William Sinkins
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  3. Andrew Keightley
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  4. Michael Kinter
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  5. William P. Schilling
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Correspondence to William P. Schilling.

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Goel, M., Sinkins, W., Keightley, A. et al. Proteomic analysis of TRPC5- and TRPC6-binding partners reveals interaction with the plasmalemmal Na+/K+-ATPase. Pflugers Arch - Eur J Physiol 451, 87–98 (2005). https://doi.org/10.1007/s00424-005-1454-y

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  • DOI: https://doi.org/10.1007/s00424-005-1454-y

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