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Synaptic logistics: Competing over shared resources
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Disruption in cargo selection can significantly impact synaptic function because synaptic receptors undergo rapid turnover via endocytosis.
“Given the rapid turnover of synaptic receptors via endocytosis, any disruption in cargo selection can significantly impact synaptic function [13].”
From Stabilizing the retromer complex rescues synaptic dysfunction and endosomal trafficking deficits in an Alzheimer’s disease mouse model (2025) · cites this paper as [13]
Section 4, “Resource bottlenecks for synaptic function” (page not provided), says glutamate receptors have among the fastest turnover rates of postsynaptic proteins and that disruptions to their supply could significantly affect responses to neurotransmitter release. It does not say that this turnover occurs via endocytosis or specifically link disrupted cargo selection to impaired synaptic function. (LLM, conf=0.86)
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López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982
Harris, K., & Stevens, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02982.1989 · Cited by 1,073
Tushev, G., Glock, C., Heumüller, M., Biever, A., Jovanovic, M., & Schuman, E. M. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.030 · Cited by 377
Hippocampal LTP and contextual learning require surface diffusion of AMPA receptors
Penn, A. C., Zhang, C. L., Georges, F., Royer, L., Breillat, C., Hosy, E., Petersen, J. D., Humeau, Y., & Choquet, D. (2017) · Nature · doi:10.1038/nature23658 · Cited by 324
Cohen, L. D., Zuchman, R., Sorokina, O., Müller, A., Dieterich, D. C., Armstrong, J. D., Ziv, T., & Ziv, N. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063191 · Cited by 215
Intra-neuronal Competition for Synaptic Partners Conserves the Amount of Dendritic Building Material
Ryglewski, S., Vonhoff, F., Scheckel, K., & Duch, C. (2017) · Neuron · doi:10.1016/j.neuron.2016.12.043 · Cited by 30
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Research works printed but not linked: 84
- Bartol, 2015, Nanoconnectomic upper bound on the variability of synaptic plasticity, elife, 4, 10.7554/eLife.10778 · DOI
- Borst, 2010, The low synaptic release probability in vivo, Trends Neurosci., 33, 259, 10.1016/j.tins.2010.03.003 · DOI
- Bressloff, 2007, Diffusion-trapping model of receptor trafficking in dendrites, Phys. Rev. E Stat. Nonlinear Soft Matter Phys., 75
- Budak, 2019, Synaptic failure differentially affects pattern formation in heterogenous networks, Front. Neural Circuits, 13, 31, 10.3389/fncir.2019.00031 · DOI
- Burute, 2019, Cellular logistics: unraveling the interplay between microtubule organization and intracellular transport, Annu. Rev. Cell Dev. Biol., 35, 29, 10.1146/annurev-cellbio-100818-125149 · DOI
- Buttgereit, 1995, A hierarchy of ATP-consuming processes in mammalian cells, Biochem. J., 312, 163, 10.1042/bj3120163 · DOI
- Cajigas, 2012, The local transcriptome in the synaptic neuropil revealed by deep sequencing and high-resolution imaging, Neuron, 74, 453, 10.1016/j.neuron.2012.02.036 · DOI · Paper page
- Chater, 2014, The role of AMPA receptors in postsynaptic mechanisms of synaptic plasticity, Front. Cell. Neurosci., 8, 401, 10.3389/fncel.2014.00401 · DOI
- Chen, 2008, Release of the styryl dyes from single synaptic vesicles in hippocampal neurons, J. Neurosci., 28, 1894, 10.1523/JNEUROSCI.4518-07.2008 · DOI
- Czöndör, 2012, Unified quantitative model of AMPA receptor trafficking at synapses, Proc. Natl. Acad. Sci. U. S. A., 109, 3522, 10.1073/pnas.1109818109 · DOI
- Darcy, 2006, Constitutive sharing of recycling synaptic vesicles between presynaptic boutons, Nat. Neurosci., 9, 315, 10.1038/nn1640 · DOI
- Donlin-Asp, 2021, Differential regulation of local mRNA dynamics and translation following long-term potentiation and depression, Proc. Natl. Acad. Sci. U. S. A., 118, 10.1073/pnas.2017578118 · DOI
- Dörrbaum, 2018, Local and global influences on protein turnover in neurons and glia, elife, 7
- Dörrbaum, 2020, Proteome dynamics during homeostatic scaling in cultured neurons, elife, 9
- Doyle, 2011, Mechanisms of dendritic mRNA transport and its role in synaptic tagging, EMBO J., 30, 3540, 10.1038/emboj.2011.278 · DOI · Paper page
- Dunwiddie, 1978, Long-term potentiation and depression of synaptic responses in the rat hippocam- pus: localization and frequency dependency, J. Physiol., 276, 353, 10.1113/jphysiol.1978.sp012239 · DOI
- Earnshaw, 2006, Biophysical model of AMPA receptor trafficking and its regulation during long-term potentiation/long-term depression, J. Neurosci., 26, 12362, 10.1523/JNEUROSCI.3601-06.2006 · DOI
- Earnshaw, 2008, Modeling the role of lateral membrane diffusion in AMPA receptor trafficking along a spiny dendrite, J. Comput. Neurosci., 25, 366, 10.1007/s10827-008-0084-8 · DOI
- Emptage, 2003, Optical quantal analysis reveals a presynaptic component of LTP at hippocampal schaffer-associational synapses, Neuron, 38, 797, 10.1016/S0896-6273(03)00325-8 · DOI
- Fernández-Alfonso, 2004, The kinetics of synaptic vesicle pool depletion at CNS synaptic terminals, Neuron, 41, 943, 10.1016/S0896-6273(04)00113-8 · DOI
- Fernandez-Alfonso, 2008, A heterogeneous “resting” pool of synaptic vesicles that is dynamically interchanged across boutons in mammalian cns synapses, Brain Cell Biol., 36, 87, 10.1007/s11068-008-9030-y · DOI
- Field, 2020, Heterosynaptic plasticity determines the set point for cortical excitatory-inhibitory balance, Neuron, 106, 842, 10.1016/j.neuron.2020.03.002 · DOI
- Fonkeu, 2019, How mRNA localization and protein synthesis sites influence dendritic protein distribution and dynamics, Neuron, 103, 1109, 10.1016/j.neuron.2019.06.022 · DOI
- Fonseca, 2004, Competing for memory: hippocampal LTP under regimes of reduced protein synthesis, Neuron, 44, 1011
- Fornasiero, 2018, Precisely measured protein lifetimes in the mouse brain reveal differences across tissues and subcellular fractions, Nat. Commun., 9, 4230, 10.1038/s41467-018-06519-0 · DOI
- Gavrilov, 2017, Functional specialization of the primate frontal lobe during cognitive control of vocalizations, Cell Rep., 21, 2393, 10.1016/j.celrep.2017.10.107 · DOI
- Glock, 2021, The translatome of neuronal cell bodies, dendrites, and axons, Proc. Natl. Acad. Sci. U. S. A., 118, 10.1073/pnas.2113929118 · DOI
- Gray, 2006, Rapid redistribution of synaptic PSD-95 in the neocortex in vivo, PLoS Biol., 4, 10.1371/journal.pbio.0040370 · DOI
- Guillaud, 2003, KIF17 dynamics and regulation of NR2B trafficking in hippocampal neurons, J. Neurosci., 23, 131, 10.1523/JNEUROSCI.23-01-00131.2003 · DOI
- Gumy, 2011, Transcriptome analysis of embryonic and adult sensory axons reveals changes in mRNA repertoire localization, RNA, 17, 85, 10.1261/rna.2386111 · DOI
- Guo, 2012, Population rate coding in recurrent neuronal networks with unreliable synapses, Cogn. Neurodyn., 6, 75, 10.1007/s11571-011-9181-x · DOI
- Hafner, 2019, Local protein synthesis is a ubiquitous feature of neuronal pre-and postsynaptic compartments, Science, 364, 10.1126/science.aau3644 · DOI · Paper page
- Hangen, 2018, Neuronal activity and intracellular calcium levels regulate intracellular transport of newly synthesized AMPAR, Cell Rep., 24, 1001, 10.1016/j.celrep.2018.06.095 · DOI
- Hannah, 1999, Synaptic vesicle biogenesis, Annu. Rev. Cell Dev. Biol., 15, 733, 10.1146/annurev.cellbio.15.1.733 · DOI
- Hanus, 2014, Synaptic control of secretory trafficking in dendrites, Cell Rep., 7, 1771, 10.1016/j.celrep.2014.05.028 · DOI
- Heine, 2008, Surface mobility of postsynaptic AMPARs tunes synaptic transmission, Science, 320, 201, 10.1126/science.1152089 · DOI · Paper page
- Jensen, 2019, Multiplex imaging relates quantal glutamate release to presynaptic ca2+ homeostasis at multiple synapses in situ, Nat. Commun., 10, 1414, 10.1038/s41467-019-09216-8 · DOI
- Kaeser, 2017, The readily releasable pool of synaptic vesicles, Curr. Opin. Neurobiol., 43, 63, 10.1016/j.conb.2016.12.012 · DOI · Paper page
- Kang, 1996, A requirement for local protein synthesis in neurotrophin-induced hippocampal synaptic plasticity, Science, 273, 1402, 10.1126/science.273.5280.1402 · DOI
- Kluever, 2022, Protein lifetimes in aged brains reveal a proteostatic adaptation linking physiological aging to neurodegeneration, Sci. Adv., 8, 10.1126/sciadv.abn4437 · DOI
- Kosik, 2016, Life at low copy number: how dendrites manage with so few mRNAs, Neuron, 92, 1168, 10.1016/j.neuron.2016.11.002 · DOI
- Kreis, 2019, ATM phosphorylation of the actin-binding protein drebrin controls oxidation stress-resistance in mammalian neurons and c. elegans, Nat. Commun., 10, 486, 10.1038/s41467-019-08420-w · DOI
- Krueger, 2003, The presynaptic release apparatus is functional in the absence of dendritic contact and highly mobile within isolated axons, Neuron, 40, 945, 10.1016/S0896-6273(03)00729-3 · DOI
- Levy, 2002, Energy-efficient neuronal computation via quantal synaptic failures, J. Neurosci., 22, 4746, 10.1523/JNEUROSCI.22-11-04746.2002 · DOI
- Lynch, 1977, Heterosynaptic depression: a postsynaptic correlate of long-term potentiation, Nature, 266, 737, 10.1038/266737a0 · DOI · Paper page
- Maday, 2014, Axonal transport: cargo-specific mechanisms of motility and regulation, Neuron, 84, 292, 10.1016/j.neuron.2014.10.019 · DOI · Paper page
- Müller, 2018, A predominantly glial origin of axonal ribosomes after nerve injury, Glia, 66, 1591, 10.1002/glia.23327 · DOI
- Nair, 2013, Super-resolution imaging reveals that AMPA receptors inside synapses are dynamically organized in nanodomains regulated by PSD95, J. Neurosci., 33, 13204, 10.1523/JNEUROSCI.2381-12.2013 · DOI · Paper page
- Oertner, 2002, Facilitation at single synapses probed with optical quantal analysis, Nat. Neurosci., 5, 657, 10.1038/nn867 · DOI
- Oh, 2015, Heterosynaptic structural plasticity on local dendritic segments of hip- pocampal ca1 neurons, Cell Rep., 10, 162, 10.1016/j.celrep.2014.12.016 · DOI
- Opazo, 2012, Regulation of AMPA receptor surface diffusion by PSD-95 slots, Curr. Opin. Neurobiol., 22, 453, 10.1016/j.conb.2011.10.010 · DOI · Paper page
- Ostroff, 2002, Polyribosomes redistribute from dendritic shafts into spines with enlarged synapses during LTP in developing rat hippocampal slices, Neuron, 35, 535, 10.1016/S0896-6273(02)00785-7 · DOI · Paper page
- Park, 2010, Single mRNA tracking in live cells, Methods Enzymol., 472, 387, 10.1016/S0076-6879(10)72003-6 · DOI
- Pastuzyn, 2018, The neuronal gene arc encodes a repurposed retrotransposon gag protein that mediates intercellular RNA transfer, Cell, 172, 275, 10.1016/j.cell.2018.03.024 · DOI · Paper page
- Perez, 2021, A functional dissection of the mRNA and locally synthesized protein population in neuronal dendrites and axons, Annu. Rev. Genet., 55, 183, 10.1146/annurev-genet-030321-054851 · DOI
- Raj, 2008, Nature, nurture, or chance: stochastic gene expression and its consequences, Cell, 135, 216, 10.1016/j.cell.2008.09.050 · DOI · Paper page
- Ramiro-Cortés, 2014, Synaptic competition in structural plasticity and cognitive function, Philos. Trans. R. Soc., B, 369, 10.1098/rstb.2013.0157 · DOI
- Reshetniak, 2020, Quantitative synap- tic biology: a perspective on techniques, numbers and expectations, Int. J. Mol. Sci., 21, 7298, 10.3390/ijms21197298 · DOI
- Rey, 2020, Nanoscale remodeling of functional synaptic vesicle pools in hebbian plasticity, Cell Rep., 30, 2006, 10.1016/j.celrep.2020.01.051 · DOI
- Rosenmund, 1993, Nonuniform probability of glutamate release at a hip- pocampal synapse, Science, 262, 754, 10.1126/science.7901909 · DOI
- Rusakov, 2020, Noisy synaptic conductance: bug or a feature?, Trends Neurosci., 43, 363, 10.1016/j.tins.2020.03.009 · DOI
- Sheng, 2011, The postsynaptic organization of synapses, Cold Spring Harb. Perspect. Biol., 3, 10.1101/cshperspect.a005678 · DOI · Paper page
- Shigeoka, 2016, Dynamic axonal translation in developing and mature visual circuits, Cell, 166, 181, 10.1016/j.cell.2016.05.029 · DOI
- Staras, 2010, A vesicle superpool spans multiple presynaptic terminals in hippocampal neurons, Neuron, 66, 37, 10.1016/j.neuron.2010.03.020 · DOI
- Stefan, 2000, Induction of plasticity in the human motor cortex by paired associative stimulation, Brain, 123, 572, 10.1093/brain/123.3.572 · DOI
- Steward, 2001, Selective targeting of newly synthesized arc mRNA to active synapses requires NMDA receptor activation, Neuron, 30, 227, 10.1016/S0896-6273(01)00275-6 · DOI
- Steward, 1998, Synaptic activation causes the mRNA for the IEG arc to localize selectively near activated postsynaptic sites on dendrites, Neuron, 21, 741, 10.1016/S0896-6273(00)80591-7 · DOI
- Sturgill, 2009, Distinct domains within PSD-95 mediate synaptic incorporation, stabilization, and activity-dependent trafficking, J. Neurosci., 29, 12845, 10.1523/JNEUROSCI.1841-09.2009 · DOI
- Sun, 2022, Logistics of neuronal protein turnover: numbers and mechanisms, Mol. Cell. Neurosci., 123
- Sylantyev, 2013, Cannabinoid- and lysophosphatidylinositol-sensitive receptor GPR55 boosts neurotransmitter release at central synapses, Proc. Natl. Acad. Sci. U. S. A., 110, 5193, 10.1073/pnas.1211204110 · DOI
- Tardin, 2003, Direct imaging of lateral movements of AMPA receptors inside synapses, EMBO J., 22, 4656, 10.1093/emboj/cdg463 · DOI · Paper page
- Tas, 2017, Differentiation between oppositely oriented microtubules controls polarized neuronal transport, Neuron, 96, 1264, 10.1016/j.neuron.2017.11.018 · DOI · Paper page
- Taylor, 2009, Axonal mRNA in uninjured and regenerating cortical mammalian axons, J. Neurosci., 29, 4697, 10.1523/JNEUROSCI.6130-08.2009 · DOI
- tom Dieck, 2015, Direct visualization of newly synthesized target proteins in situ, Nat. Methods, 12, 411, 10.1038/nmeth.3319 · DOI
- Triesch, 2018, Competition for synaptic building blocks shapes synaptic plasticity, elife, 7, 10.7554/eLife.37836 · DOI
- Tsuriel, 2006, Local sharing as a predominant determinant of synaptic matrix molecular dynamics, PLoS Biol., 4, 10.1371/journal.pbio.0040271 · DOI
- Turrel, 2022, Transient active zone remodeling in the drosophila mushroom body supports memory, Curr. Biol., 32, 4900, 10.1016/j.cub.2022.10.017 · DOI
- Wagle, 2023, Computational insights into mrna and protein dynamics underlying synaptic plasticity rules, Mol. Cell. Neurosci., 125, 10.1016/j.mcn.2023.103846 · DOI
- Westphal, 2008, Video-rate far-field optical nanoscopy dissects synaptic vesicle movement, Science, 320, 246, 10.1126/science.1154228 · DOI
- Wilhelm, 2014, Composition of isolated synaptic boutons reveals the amounts of vesicle trafficking proteins, Science, 344, 1023, 10.1126/science.1252884 · DOI · Paper page
- Wu, 2016, Translation dynamics of single mRNAs in live cells and neurons, Science, 352, 1430, 10.1126/science.aaf1084 · DOI
- Yoon, 2016, Glutamate-induced RNA localization and translation in neurons, Proc. Natl. Acad. Sci. U. S. A., 113, E6877, 10.1073/pnas.1614267113 · DOI
- Ziemann, 1996, Interaction between intracortical inhibition and facilitation in human motor cortex, J. Physiol., 496, 873, 10.1113/jphysiol.1996.sp021734 · DOI
- Ziv, 2014, Presynaptic and postsynaptic scaffolds: dynamics fast and slow, Neuroscientist, 20, 439, 10.1177/1073858414523321 · DOI
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Ramonet, D., Daerr, A., & Hallbeck, M. (2025) · Acta Neuropathologica Communications · doi:10.1186/s40478-025-02096-8 · Cited by 7
Metadata
- Authors
- Hafner, A.-S., & Triesch, J.
- Venue
- Molecular and Cellular Neuroscience
- Publisher
- Elsevier BV
- Published
- 2023-06
- Volume
- 125
- Pages
- 103858
- ISSN
- 1044-7431
- Cited by
- 2
- References
- 6
- Language
- en
- Licence
- Funders
- Horizon 2020
- European Research Council (101076961)
- Deutsche Forschungsgemeinschaft (TR881/8-1, SPP-2041)
- Johanna Quandt Stiftung
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