Filopodia are a structural substrate for silent synapses in adult neocortex
Abstract
Newly generated excitatory synapses in the mammalian cortex lack sufficient AMPA-type glutamate receptors to mediate neurotransmission, resulting in functionally silent synapses that require activity-dependent plasticity to mature. Silent synapses are abundant in early development, during which they mediate circuit formation and refinement, but they are thought to be scarce in adulthood 1 . However, adults retain a capacity for neural plasticity and flexible learning that suggests that the formation of new connections is still prevalent. Here we used super-resolution protein imaging to visualize synaptic proteins at 2,234 synapses from layer 5 pyramidal neurons in the primary visual cortex of adult mice. Unexpectedly, about 25% of these synapses lack AMPA receptors. These putative silent synapses were located at the tips of thin dendritic protrusions, known as filopodia, which were more abundant by an order of magnitude than previously believed (comprising about 30% of all dendritic protrusions). Physiological experiments revealed that filopodia do indeed lack AMPA-receptor-mediated transmission, but they exhibit NMDA-receptor-mediated synaptic transmission. We further showed that functionally silent synapses on filopodia can be unsilenced through Hebbian plasticity, recruiting new active connections into a neuron's input matrix. These results challenge the model that functional connectivity is largely fixed in the adult cortex and demonstrate a new mechanism for flexible con…
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There is a population of synapses that lack AMPARs but have a normal complement of NMDARs, referred to as silent synapses.
“First, there is a population of synapses that lack AMPARs but have a normal complement of NMDARs and are referred to as “silent synapses.””
From Synaptic memory and CaMKII (2023) · cites this paper as [240]
Filipodia account for roughly 30% of synapses in the mature brain.
“The anatomical substrate for silent synapses is fingerlike dendritic protrusions referred to as filipodia (245), which account for roughly 30% of synapses in the mature brain (240).”
From Synaptic memory and CaMKII (2023) · cites this paper as [240]
Silent synapses are abundant in the mature brain.
“a recent elegant study has shown an abundance of silent synapses in mature brain (240).”
From Synaptic memory and CaMKII (2023) · cites this paper as [240]
LTP-producing stimuli cause rapid accumulation of AMPARs at silent synapses, referred to as unsilencing.
“LTP-producing stimuli cause a rapid accumulation of AMPARs referred to as “unsilencing” (238–241).”
From Synaptic memory and CaMKII (2023) · cites this paper as [240]
LTP-induced unsilencing of synapses indicates that LTP can be all or none.
“The LTP-induced unsilencing of synapses (238–240) certainly indicates that LTP can be all or none.”
From Synaptic memory and CaMKII (2023) · cites this paper as [240]
Synapses with few, if any, AMPARs, referred to as silent synapses, form a distinct anatomical class referred to as filopodial synapses, in contrast to classical spine synapses.
“Recent work has shown that synapses with few, if any, AMPARs, referred to as silent synapses (238, 239), form a distinct anatomical class referred to as filopodial synapses, in contrast to classical spine synapses (240).”
From Synaptic memory and CaMKII (2023) · cites this paper as [240]
Cites
Long-term dendritic spine stability in the adult cortex
Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198 · see citing works
Developmental regulation of spine motility in the mammalian central nervous system
Dunaevsky, A., Tashiro, A., Majewska, A., Mason, C., & Yuste, R. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13438 · Cited by 412 · see citing works
Structure and function of a neocortical synapse
Holler, S., Köstinger, G., Martin, K. A. C., Schuhknecht, G. F. P., & Stratford, K. J. (2021) · Nature · doi:10.1038/s41586-020-03134-2 · Cited by 249 · see citing works
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Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126 · see citing works
“Presumably in this LLPS reorganization, PSD-95 molecules previously not available for AMPAR/TARPs become unmasked.”
BackgroundResultInfluential
- Authors
- Vardalaki, D., Chung, K., & Harnett, M. T.
- Affiliations
- McGovern Institute for Brain Research (US)
- Broad Institute (US)
- Corresponding author
- Harnett, Mark T.
- Venue
- Nature
- Published
- 2022-11-30
- Volume
- 612
- Issue
- 7939
- Pages
- 323-327
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W4311587806
- Cited by
- 96
- References
- 3
- Citations by year
- 2026: 11 · 2025: 30 · 2024: 28 · 2023: 26 · 2022: 1
- FWCI
- 9.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS106031)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- silent synapses, filopodia, AMPA receptors, NMDA receptor, synaptic transmission, Hebbian plasticity, layer 5 pyramidal neurons, primary visual cortex, dendritic protrusions, synaptic plasticity, adult neurogenesis
- MeSH terms
- Animals, Mammals, Records, Mice
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