New Concepts in Synaptic Biology Derived from Single-Molecule Imaging
Open accessAbstract
Single-molecule approaches give access to the full distribution of molecule behaviors and overcome the averaging intrinsic to bulk measurement methods. They allow access to complex processes where a given molecule can have heterogeneous properties over time. Recent developments in single-molecule imaging technologies have been followed by their wide application in cellular biology and are leading to the unraveling of new mechanisms related to molecular movements. They are shaping new concepts in the dynamic equilibria of complex biological macromolecular assemblies such as synapses. These advances were made possible thanks to improvements in visualization approaches combined with new strategies to label proteins with nanoprobes. In this primer, we will review the different approaches used to track single molecules in live neurons, compare them to bulk measurements, and discuss the different concepts that have emerged from their application to synaptic biology.
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The surface mobility of neurotransmitter receptors is dynamically regulated to control synaptic activity and is a key component underlying plasticity at nerve terminals.
“The surface mobility of neurotransmitter receptors is dynamically regulated to control synaptic activity and is emerging as another key component underlying plasticity at nerve terminals.40,53,54”
From The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines (2014) · cites this paper as [53]
The passages under “Concepts that Have Emerged from Single-Molecule Imaging in Synaptic Biology” report that receptor movements are modulated by neuronal activity. The passage on fast synaptic transmission says AMPA-receptor lateral diffusion affects synaptic signaling and recovery from postsynaptic depression. These support a role in synaptic activity and plasticity, but they concern postsynaptic receptors, not plasticity specifically at nerve terminals. (LLM, conf=0.84)
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Cites
The Postsynaptic Architecture of Excitatory Synapses: A More Quantitative View
Sheng, M., & Hoogenraad, C. C. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.060805.160029 · Cited by 1,003 · see citing works
Recycling Endosomes Supply AMPA Receptors for LTP
Park, M., Penick, E. C., Edwards, J. G., Kauer, J. A., & Ehlers, M. D. (2004) · Science · doi:10.1126/science.1102026 · Cited by 730 · see citing works
Subunit-specific temporal and spatial patterns of AMPA receptor exocytosis in hippocampal neurons
Passafaro, M., Piëch, V., & Sheng, M. (2001) · Nature Neuroscience · doi:10.1038/nn0901-917 · Cited by 655 · see citing works
Regulation of AMPA receptor lateral movements
Borgdorff, A. J., & Choquet, D. (2002) · Nature · doi:10.1038/nature00780 · Cited by 542 · see citing works
Self-citationAshby, M. C., Maier, S. R., Nishimune, A., & Henley, J. M. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1235-06.2006 · Cited by 302 · see citing works
Xu, D., Hopf, C., Reddy, R., Cho, R. W., Guo, L., Lanahan, A., Petralia, R. S., Wenthold, R. J., O'Brien, R. J., & Worley, P. (2003) · Neuron · doi:10.1016/s0896-6273(03)00463-x · Cited by 265 · see citing works
Photoinactivation of native AMPA receptors reveals their real-time trafficking
Adesnik, H., Nicoll, R. A., & England, P. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.11.030 · Cited by 234 · see citing works
Richards, D. A., De Paola, V., Caroni, P., Gähwiler, B. H., & McKinney, R. A. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.062091 · Cited by 49 · see citing works
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Research works printed but not linked: 5
- [2]2. Alivisatos, P. The use of nanocrystals in biological detection Nat. Biotechnol. 2004; 22:47-52 Crossref Scopus (1756) Google Scholar
- [3]3. Allison, D.W. ∙ Gelfand, V.I. ∙ Spector, I. ... Role of actin in anchoring postsynaptic receptors in cultured hippocampal neurons: differential attachment of NMDA versus AMPA receptors J. Neurosci. 1998; 18:2423-2436 Crossref PubMed Google Scholar
- [4]4. Anderson, R.G. ∙ Jacobson, K. A role for lipid shells in targeting proteins to caveolae, rafts, and other lipid domains Science. 2002; 296:1821-1825 Crossref Scopus (765) PubMed Google Scholar
- [5]5. Ashby, M.C. ∙ De La Rue, S.A. ∙ Ralph, G.S. ... Removal of AMPA receptors (AMPARs) from synapses is preceded by transient endocytosis of extrasynaptic AMPARs J. Neurosci. 2004; 24:5172-5176 Crossref Scopus (118) PubMed Google Scholar
- [7]7. Axelrod, D. ∙ Koppel, D.E. ∙ Schlessinger, J. ... Mobility measurement by analysis of fluorescence photobleaching recovery kinetics Biophys. J. 1976; 16:1055-1069
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Sheng, M., & Kim, E. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005678 · Cited by 603 · see citing works
Unraveling mechanisms of homeostatic synaptic plasticity
Pozo, K., & Goda, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.028 · Cited by 565 · see citing works
The dual role of the extracellular matrix in synaptic plasticity and homeostasis
Dityatev, A., Schachner, M., & Sonderegger, P. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2898 · Cited by 559 · see citing works
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Self-citationBrain temperature and its fundamental properties: a review for clinical neuroscientists
Wang, H., Wang, B., Normoyle, K. P., Jackson, K., Spitler, K., Sharrock, M. F., Miller, C. M., Best, C., Llano, D., & Du, R. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00307 · Cited by 356 · see citing works
Syntaxin-4 defines a domain for activity-dependent exocytosis in dendritic spines
Kennedy, M. J., Davison, I. G., Robinson, C. G., & Ehlers, M. D. (2010) · Cell · doi:10.1016/j.cell.2010.02.042 · Cited by 294 · see citing works
From the stochasticity of molecular processes to the variability of synaptic transmission
Ribrault, C., Sekimoto, K., & Triller, A. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3025 · Cited by 198 · see citing works
Self-citationA three-step model for the synaptic recruitment of AMPA receptors
Opazo, P., & Choquet, D. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.014 · Cited by 190 · see citing works
Self-citationPathania, M., Davenport, E. C., Muir, J., Sheehan, D. F., López-Doménech, G., & Kittler, J. T. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.16 · Cited by 189 · see citing works
Muir, J., Arancibia-Carcamo, I. L., MacAskill, A. F., Smith, K. R., Griffin, L. D., & Kittler, J. T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000589107 · Cited by 158 · see citing works
Converting juvenile into adult plasticity: a role for the brain's extracellular matrix
Gundelfinger, E. D., Frischknecht, R., Choquet, D., & Heine, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07253.x · Cited by 136 · see citing works
Self-citationMolecular genetics and imaging technologies for circuit-based neuroanatomy
Arenkiel, B. R., & Ehlers, M. D. (2009) · Nature · doi:10.1038/nature08536 · Cited by 78 · see citing works
- Authors
- Triller, A., & Choquet, D.
- Affiliations
- Inserm (FR)
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Triller, Antoine
- Choquet, Daniel
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2008-08
- Volume
- 59
- Issue
- 3
- Pages
- 359-374
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2021845085
- Cited by
- 262
- References
- 8
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 3 · 2023: 6 · 2022: 9 · 2021: 13 · 2020: 8 · 2019: 7 · 2018: 15 · 2017: 16 · 2016: 11 · 2015: 16 · 2014: 25 · 2013: 20 · 2012: 31
- FWCI
- 2.40
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Advanced Fluorescence Microscopy Techniques
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- single-molecule imaging, single-molecule tracking, live neurons, nanoprobes, protein labeling, molecular heterogeneity, synaptic dynamics, macromolecular complexes
- MeSH terms
- Animals, Diagnostic Imaging, Models, Biological, Neurons, Synapses, Nanotechnology
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