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Critical role of TRPC6 channels in the formation of excitatory synapses

Abstract

The transient receptor potential canonical (TRPC) channels are Ca2+-permeable, nonselective cation channels with different biological functions, but their roles in brain are largely unknown. Here we report that TRPC6 was localized to excitatory synapses and promoted their formation via a CaMKIV-CREB–dependent pathway. TRPC6 transgenic mice showed enhancement in spine formation, and spatial learning and memory in Morris water maze. These results reveal a previously unknown role of TRPC6 in synaptic and behavioral plasticity.

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Figure 1: TRPC6 was localized to excitatory postsynapses.
Figure 2: TRPC6 promoted the formation of dendritic spines and excitatory synapses via a CaMKIV-CREB–dependent pathway.
Figure 3: TRPC6 transgenic mice showed enhancement in spine density, spatial learning and memory.

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References

  1. Montell, C., Birnbaumer, L. & Flockerzi, V. Cell 108, 595–598 (2002).

    Article  CAS  Google Scholar 

  2. Jungnickel, M.K. et al. Nat. Cell Biol. 3, 499–502 (2001).

    Article  CAS  Google Scholar 

  3. Greka, A. et al. Nat. Neurosci. 6, 837–845 (2003).

    Article  CAS  Google Scholar 

  4. Li, Y. et al. Nature 434, 894–898 (2005).

    Article  CAS  Google Scholar 

  5. Kim, S.J. et al. Nature 426, 285–291 (2003).

    Article  CAS  Google Scholar 

  6. Li, H.S., Xu, X.Z. & Montell, C. Neuron 24, 261–273 (1999).

    Article  CAS  Google Scholar 

  7. Riedel, G., Platt, B. & Micheau, J. Behav. Brain Res. 140, 1–47 (2003).

    Article  CAS  Google Scholar 

  8. Minichiello, L. et al. Neuron 36, 121–137 (2002).

    Article  CAS  Google Scholar 

  9. Zhou, Q., Homma, K.J. & Poo, M.M. Neuron 44, 749–757 (2004).

    Article  CAS  Google Scholar 

  10. Hering, H. & Sheng, M. Nat. Rev. Neurosci. 2, 880–888 (2001).

    Article  CAS  Google Scholar 

  11. Kang, H. et al. Cell 106, 771–783 (2001).

    Article  CAS  Google Scholar 

  12. Pang, P.T. & Lu, B. Ageing Res. Rev. 3, 407–430 (2004).

    Article  CAS  Google Scholar 

  13. Tang, Y.P. et al. Nature 401, 63–69 (1999).

    Article  CAS  Google Scholar 

  14. Vicario-Abejon, C., Owens, D., McKay, R. & Segal, M. Nat. Rev. Neurosci. 3, 965–974 (2002).

    Article  CAS  Google Scholar 

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Acknowledgements

We thank J.W. Putney, Jr., T. Gudermann, D.J. Linden, M.E. Greenberg and S.J. Elledge for providing constructs, W.P. Schilling for TRPC1 antibodies and Q. Hu for confocal imaging. This work was supported by grants from KSCX2-YW-R-099 (Chinese Academy of Science), the 973 program (2006CB806600) and projects 30621062, 30711120566, U0632006 from the National Natural Science Foundation of China.

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Contributions

J.Z. and W.D. conducted the experiments and wrote the manuscript. K.Z. carried out the recording, and Y.T., H.Y. and Y.J. prepared some of the constructs. Y.D. helped with the transgenic mice and Y.W. supervised the project and wrote the manuscript.

Corresponding author

Correspondence to Yizheng Wang.

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Supplementary Figures 1–9 and Supplementary Methods (PDF 2521 kb)

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Zhou, J., Du, W., Zhou, K. et al. Critical role of TRPC6 channels in the formation of excitatory synapses. Nat Neurosci 11, 741–743 (2008). https://doi.org/10.1038/nn.2127

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