Abstract
Sensory experience is necessary for normal cortical development. This has been shown by sensory deprivation and pharmacological perturbation of the cortex. Because these manipulations affect the cortical network as a whole, the role of postsynaptic cellular properties during experience-dependent development is unclear. Here we addressed the developmental role of somatodendritic excitability, which enables postsynaptic spike timing–dependent forms of plasticity, in rat somatosensory cortex. We used short interfering RNA (siRNA)-based knockdown of Na+ channels to suppress the somatodendritic excitability of small numbers of layer 2/3 pyramidal neurons in the barrel cortex, without altering the ascending sensory pathway. In vivo recordings from siRNA-expressing cells revealed that this manipulation interfered with the normal developmental strengthening of sensory responses. The sensory responsiveness of neighboring cortical neurons was unchanged, indicating that the cortical network was unchanged. We conclude that somatodendritic excitability of the postsynaptic neuron is needed for the regulation of synaptic strength in the developing sensory cortex.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$189.00 per year
only $15.75 per issue
Rent or buy this article
Get just this article for as long as you need it
$39.95
Prices may be subject to local taxes which are calculated during checkout







References
Sur, M. & Leamey, C.A. Development and plasticity of cortical areas and networks. Nat. Rev. Neurosci. 2, 251–262 (2001).
Hubel, D.H. & Wiesel, T.N. Receptive fields of cells in striate cortex of very young, visually inexperienced kittens. J. Neurophysiol. 26, 994–1002 (1963).
Hubel, D.H. & Wiesel, T.N. Binocular interaction in striate cortex of kittens reared with artificial squint. J. Neurophysiol. 28, 1041–1059 (1965).
Stryker, M.P. & Strickland, S.L. Physiological segregation of ocular dominance columns depends on the pattern of afferent electrical activity. Invest. Ophthalmol. Vis. Sci. 25, 278 (1984).
Bi, G. & Poo, M. Synaptic modification by correlated activity: Hebb's postulate revisited. Annu. Rev. Neurosci. 24, 139–166 (2001).
Song, S. & Abbott, L.F. Cortical development and remapping through spike timing-dependent plasticity. Neuron 32, 339–350 (2001).
Markram, H., Lubke, J., Frotscher, M. & Sakmann, B. Regulation of synaptic efficacy by coincidence of postsynaptic action potentials and EPSPs. Science 275, 213–215 (1997).
Magee, J.C. & Johnston, D. A synaptically controlled, associative signal for Hebbian plasticity in hippocampal neurons. Science 275, 209–213 (1997).
Golding, N.L., Staff, N.P. & Spruston, N. Dendritic spikes as a mechanism for cooperative long-term potentiation. Nature 418, 326–331 (2002).
Stuart, G.J. & Sakmann, B. Active propagation of somatic action potentials into neocortical pyramidal cell dendrites. Nature 367, 69–72 (1994).
Regehr, W., Kehoe, J.S., Ascher, P. & Armstrong, C. Synaptically triggered action potentials in dendrites. Neuron 11, 145–151 (1993).
Woolsey, T.A. & Van der Loos, H. The structural organization of layer IV in the somatosensory region (SI) of mouse cerebral cortex. The description of a cortical field composed of discrete cytoarchitectonic units. Brain Res. 17, 205–242 (1970).
Simons, D.J. & Land, P.W. Early experience of tactile stimulation influences organization of somatic sensory cortex. Nature 326, 694–697 (1987).
Fox, K. A critical period for experience-dependent synaptic plasticity in rat barrel cortex. J. Neurosci. 12, 1826–1838 (1992).
Glazewski, S. & Fox, K. Time course of experience-dependent synaptic potentiation and depression in barrel cortex of adolescent rats. J. Neurophysiol. 75, 1714–1729 (1996).
Stern, E.A., Maravall, M. & Svoboda, K. Rapid development and plasticity of layer 2/3 maps in rat barrel cortex in vivo. Neuron 31, 305–315 (2001).
Shepherd, G.M., Pologruto, T.A. & Svoboda, K. Circuit analysis of experience-dependent plasticity in the developing rat barrel cortex. Neuron 38, 277–289 (2003).
Bureau, I., Shepherd, G.M. & Svoboda, K. Precise development of functional and anatomical columns in the neocortex. Neuron 42, 789–801 (2004).
Margrie, T.W. et al. Targeted whole-cell recordings in the mammalian brain in vivo. Neuron 39, 911–918 (2003).
Dittgen, T. et al. Lentivirus-based genetic manipulations of cortical neurons and their optical and electrophysiological monitoring in vivo. Proc. Natl. Acad. Sci. USA 101, 18206–18211 (2004).
Komai, S., Denk, W., Osten, P., Brecht, M. & Margrie, T.W. Two-photon targeted patching (TPTP) in vivo. Nat. Protocols 1, 648–653 (2006).
Elbashir, S.M. et al. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature 411, 494–498 (2001).
Denk, W., Strickler, J.H. & Webb, W.W. Two-photon laser scanning fluorescence microscopy. Science 248, 73–76 (1990).
Yu, F.H. & Catterall, W.A. Overview of the voltage-gated sodium channel family. Genome Biol. 4, 207 (2003).
Mainen, Z.F. & Sejnowski, T.J. Influence of dendritic structure on firing pattern in model neocortical neurons. Nature 382, 363–366 (1996).
Mainen, Z.F., Joerges, J., Huguenard, J.R. & Sejnowski, T.J. A model of spike initiation in neocortical pyramidal neurons. Neuron 15, 1427–1439 (1995).
Palmer, L.M. & Stuart, G.J. Site of action potential initiation in layer 5 pyramidal neurons. J. Neurosci. 26, 1854–1863 (2006).
Waters, J., Larkum, M., Sakmann, B. & Helmchen, F. Supralinear Ca2+ influx into dendritic tufts of layer 2/3 neocortical pyramidal neurons in vitro and in vivo. J. Neurosci. 23, 8558–8567 (2003).
Moore, C.I. & Nelson, S.B. Spatio-temporal subthreshold receptive fields in the vibrissa representation of rat primary somatosensory cortex. J. Neurophysiol. 80, 2882–2892 (1998).
Brecht, M., Roth, A. & Sakmann, B. Dynamic receptive fields of reconstructed pyramidal cells in layers 3 and 2 of rat somatosensory barrel cortex. J. Physiol. (Lond.) 553, 243–265 (2003).
Petersen, C.C., Hahn, T.T., Mehta, M., Grinvald, A. & Sakmann, B. Interaction of sensory responses with spontaneous depolarization in layer 2/3 barrel cortex. Proc. Natl. Acad. Sci. USA 100, 13638–13643 (2003).
Sachdev, R.N., Ebner, F.F. & Wilson, C.J. Effect of subthreshold up and down states on the whisker-evoked response in somatosensory cortex. J. Neurophysiol. 92, 3511–3521 (2004).
Stuart, G. & Sakmann, B. Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons. Neuron 15, 1065–1076 (1995).
Lendvai, B., Stern, E.A., Chen, B. & Svoboda, K. Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo. Nature 404, 876–881 (2000).
Micheva, K.D. & Beaulieu, C. Quantitative aspects of synaptogenesis in the rat barrel field cortex with special reference to GABA circuitry. J. Comp. Neurol. 373, 340–354 (1996).
Holtmaat, A.J. et al. Transient and persistent dendritic spines in the neocortex in vivo. Neuron 45, 279–291 (2005).
Zuo, Y., Yang, G., Kwon, E. & Gan, W.B. Long-term sensory deprivation prevents dendritic spine loss in primary somatosensory cortex. Nature 436, 261–265 (2005).
Feldmeyer, D., Lubke, J., Silver, R.A. & Sakmann, B. Synaptic connections between layer 4 spiny neurone-layer 2/3 pyramidal cell pairs in juvenile rat barrel cortex: physiology and anatomy of interlaminar signalling within a cortical column. J. Physiol. (Lond.) 538, 803–822 (2002).
Yuste, R. & Bonhoeffer, T. Genesis of dendritic spines: insights from ultrastructural and imaging studies. Nat. Rev. Neurosci. 5, 24–34 (2004).
Zuo, Y., Lin, A., Chang, P. & Gan, W.B. Development of long-term dendritic spine stability in diverse regions of cerebral cortex. Neuron 46, 181–189 (2005).
Feldman, D.E. & Brecht, M. Map plasticity in somatosensory cortex. Science 310, 810–815 (2005).
Reiter, H.O. & Stryker, M.P. Neural plasticity without postsynaptic action potentials: less-active inputs become dominant when kitten visual cortical cells are pharmacologically inhibited. Proc. Natl. Acad. Sci. USA 85, 3623–3627 (1988).
Bear, M.F., Kleinschmidt, A., Gu, Q.A. & Singer, W. Disruption of experience-dependent synaptic modifications in striate cortex by infusion of an NMDA receptor antagonist. J. Neurosci. 10, 909–925 (1990).
Schlaggar, B.L., Fox, K. & O'Leary, D.D. Postsynaptic control of plasticity in developing somatosensory cortex. Nature 364, 623–626 (1993).
Ruthazer, E.S. You're perfect, now change–redefining the role of developmental plasticity. Neuron 45, 825–828 (2005).
Schuett, S., Bonhoeffer, T. & Hubener, M. Pairing-induced changes of orientation maps in cat visual cortex. Neuron 32, 325–337 (2001).
Meliza, C.D. & Dan, Y. Receptive-field modification in rat visual cortex induced by paired visual stimulation and single-cell spiking. Neuron 49, 183–189 (2006).
Allen, C.B., Celikel, T. & Feldman, D.E. Long-term depression induced by sensory deprivation during cortical map plasticity in vivo. Nat. Neurosci. 6, 291–299 (2003).
Celikel, T., Szostak, V.A. & Feldman, D.E. Modulation of spike timing by sensory deprivation during induction of cortical map plasticity. Nat. Neurosci. 7, 534–541 (2004).
Lisman, J. & Spruston, N. Postsynaptic depolarization requirements for LTP and LTD: a critique of spike timing-dependent plasticity. Nat. Neurosci. 8, 839–841 (2005).
Acknowledgements
We thank P.H. Seeburg for long-term support; C. Grosskurth, S. Gruenewald, M. Kaiser and J. Müller for technical assistance; and R. Bruno, T. Celikel, D. Haydon-Wallace, M. Häusser, T. Margrie, M. Mehta, B. Sakmann and P.H. Seeburg for comments on the manuscript. This work was supported by the Max Planck Society.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Supplementary information
Supplementary Fig. 1
Correlation between AP amplitude and AP threshold in Nav1.1-1.3 knockdown layer 2/3 pyramidal neurons in vitro. (PDF 510 kb)
Supplementary Fig. 2
Nav1.1–1.3 knock-down reduces sensory-evoked responses. (PDF 527 kb)
Supplementary Fig. 3
Correlation between sePSP amplitude and number of infected Nav1.1–1.3 knockdown cells in vivo. (PDF 417 kb)
Rights and permissions
About this article
Cite this article
Komai, S., Licznerski, P., Cetin, A. et al. Postsynaptic excitability is necessary for strengthening of cortical sensory responses during experience-dependent development. Nat Neurosci 9, 1125–1133 (2006). https://doi.org/10.1038/nn1752
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/nn1752
This article is cited by
-
A Bcl-xL–Drp1 complex regulates synaptic vesicle membrane dynamics during endocytosis
Nature Cell Biology (2013)
-
Transfection via whole-cell recording in vivo: bridging single-cell physiology, genetics and connectomics
Nature Neuroscience (2011)
-
Bcl-xL regulates metabolic efficiency of neurons through interaction with the mitochondrial F1FO ATP synthase
Nature Cell Biology (2011)
-
Transfection of Nerve Cells
Neuroscience and Behavioral Physiology (2010)
-
Distinct contributions of Nav1.6 and Nav1.2 in action potential initiation and backpropagation
Nature Neuroscience (2009)