Sodium channels amplify spine potentials
Open accessAbstract
Dendritic spines mediate most excitatory synapses in the brain. Past theoretical work and recent experimental evidence have suggested that spines could contain sodium channels. We tested this by measuring the effect of the sodium channel blocker tetrodotoxin (TTX) on depolarizations generated by two-photon uncaging of glutamate on spines from mouse neocortical pyramidal neurons. In practically all spines examined, uncaging potentials were significantly reduced by TTX. This effect was postsynaptic and spatially localized to the spine and occurred with uncaging potentials of different amplitudes and in spines of different neck lengths. Our data confirm that spines from neocortical pyramidal neurons are electrically isolated from the dendrite and indicate that they have sodium channels and are therefore excitable structures. Spine sodium channels could boost synaptic potentials and facilitate action potential backpropagation.
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Active properties of dendritic spines play an important role in interactions between multiple synaptic inputs in dendritic computation.
“These active properties of dendritic spines are thought to play an important role in the interactions between multiple synaptic inputs in dendritic computation (Araya et al., 2007; Harnett et al., 2012).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Araya et al., 2007
Opening of sodium and calcium channels boosts local depolarization, while opening of potassium channels decreases local input resistance and results in smaller synaptic potentials.
“Opening of sodium and calcium channels boosts local depolarization (Araya et al., 2007; Bloodgood et al., 2009; Holbro et al., 2010; Carter et al., 2012; Hao and Oertner, 2012), while opening of potassium channels decreases local input resistance and results in smaller synaptic potentials (Ngo-Anh et al., 2005; Giessel and Sabatini, 2010).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Araya et al., 2007
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Matsuzaki, M., Ellis-Davies, G. C. R., Nemoto, T., Miyashita, Y., Iino, M., & Kasai, H. (2001) · Nature Neuroscience · doi:10.1038/nn736 · Cited by 1,563 · see citing works
Cortical area and species differences in dendritic spine morphology
Benavides-Piccione, R., Ballesteros-Yáñez, I., DeFelipe, J., & Yuste, R. (2002) · Journal of Neurocytology · doi:10.1023/a:1024134312173 · Cited by 207 · see citing works
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Dendritic spines and distributed circuits
Yuste, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.024 · Cited by 298 · see citing works
Self-citationActivity-dependent dendritic spine neck changes are correlated with synaptic strength
Araya, R., Vogels, T. P., & Yuste, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321869111 · Cited by 197 · see citing works
Self-citationBarriers in the brain: resolving dendritic spine morphology and compartmentalization
Adrian, M., Kusters, R., Wierenga, C. J., Storm, C., Hoogenraad, C. C., & Kapitein, L. C. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00142 · Cited by 62 · see citing works
“These active properties of dendritic spines are thought to play an important role in the interactions between multiple synaptic inputs in dendritic computation (Araya et al., 2007; Harnett et al., 2012).”
Popovic, M. A., Gao, X., Carnevale, N. T., & Zecevic, D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs320 · Cited by 35 · see citing works
- Authors
- Araya, R., Nikolenko, V., Eisenthal, K. B., & Yuste, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Columbia University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-07-24
- Volume
- 104
- Issue
- 30
- Pages
- 12347-12352
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1924793
- OpenAlex
- W2127198126
- Cited by
- 80
- References
- 2
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 6 · 2021: 5 · 2020: 5 · 2019: 3 · 2018: 2 · 2017: 4 · 2016: 3 · 2015: 7 · 2014: 5 · 2013: 5 · 2012: 5
- FWCI
- 2.79
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Columbia Academic Commons (Columbia University)
- Funders
- National Science Foundation
- Drexel University
- College of Medicine, Drexel University
- National Eye Institute
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- dendritic spines, sodium channels, tetrodotoxin, glutamate uncaging, neocortical pyramidal neurons, action potential backpropagation, postsynaptic potentials, excitatory synapses
- MeSH terms
- Action Potentials, Animals, Dendrites, Electrophysiology, Mice, Inbred C57BL, Synapses, Tetrodotoxin, Sodium Channels, Mice
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