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Axonal transport: Driving synaptic function
Open accessAbstract
From trafficking to maintenance: Neurons are remarkably polarized in that proteins made in the cytosol often need to travel many tens or hundreds of cell body lengths along axons to their sites of action in the synapse. Axonal transport of these components is driven by molecular motors along axonal microtubules. Guedes-Dias and Holzbaur review the cell biology of axonal transport and highlight the roles this fundamental process plays in organismal health. Science , this issue p. eaaw9997
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“Further, given that the centrum semiovale had the second highest estimated effect size (Cohen’s d of 0.51) and that we saw an effect of intervention duration for the centrum semiovale, we cannot exclude that the SSRI intervention could have an effect on the specific binding in the white matter, e.g. due to increased axonal transport of newly synthesized synaptic vesicle precursors [56].”
From Effects of escitalopram on synaptic density in the healthy human brain: a randomized controlled trial (2023) · cites this paper as [56]
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Molecular anatomy of a trafficking organelle
Takamori, S., Holt, M., Stenius, K., Lemke, E. A., Grønborg, M., Riedel, D., Urlaub, H., Schenck, S., Brügger, B., Ringler, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.10.030 · Cited by 2,373
Kanai, Y., Dohmae, N., & Hirokawa, N. (2004) · Neuron · doi:10.1016/j.neuron.2004.07.022 · Cited by 1,109
Differential Regulation of Dynein and Kinesin Motor Proteins by Tau
Dixit, R., Ross, J. L., Goldman, Y. E., & Holzbaur, E. L. F. (2008) · Science · doi:10.1126/science.1152993 · Cited by 1,012
Self-citationQuantitative ultrastructural analysis of hippocampal excitatory synapses
Schikorski, T., & Stevens, C. F. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05858.1997 · Cited by 997
Mutant dynactin in motor neuron disease
Puls, I., Jonnakuty, C., LaMonte, B. H., Holzbaur, E. L. F., Tokito, M. K., MANN, E. A., Floeter, M. K., Bidus, K., Drayna, D. T., Oh, S. J., et al. (2003) · Nature Genetics · doi:10.1038/ng1123 · Cited by 973
Self-citationSaudou, F., & Humbert, S. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.003 · Cited by 945
Control of microtubule organization and dynamics: Two ends in the limelight
Akhmanova, A., & Steinmetz, M. O. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4084 · Cited by 895
The Mechanism of Ca2+-Dependent Regulation of Kinesin-Mediated Mitochondrial Motility
Wang, X., & Schwarz, T. L. (2009) · Cell · doi:10.1016/j.cell.2008.11.046 · Cited by 871
Activity-driven local ATP synthesis is required for synaptic function
Rangaraju, V., Calloway, N., & Ryan, T. A. (2014) · Cell · doi:10.1016/j.cell.2013.12.042 · Cited by 836
Neuropeptide Transmission in Brain Circuits
van den Pol, A. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.014 · Cited by 810
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Frühbeis, C., Kuo, W. P., Müller, C., Barth, K., Peris, L., Tenzer, S., Möbius, W., Werner, H. B., Nave, K., Fröhlich, D., et al. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000621 · Cited by 201
Kuijpers, M., Kochlamazashvili, G., Stumpf, A., Puchkov, D., Swaminathan, A., Lucht, M. T., Krause, E., Maritzen, T., Schmitz, D., & Haucke, V. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.005 · Cited by 170
Boecker, C. A., Goldsmith, J., Dou, D., Cajka, G. G., & Holzbaur, E. L. F. (2021) · Current Biology · doi:10.1016/j.cub.2021.02.061 · Cited by 172
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Barron, J. C., Hurley, E. P., & Parsons, M. P. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.689332 · Cited by 85
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Tesco, G., & Lomoio, S. (2022) · Seminars in Immunology · doi:10.1016/j.smim.2022.101628 · Cited by 102
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Hilton, B. J., Griffin, J. M., Fawcett, J. W., & Bradke, F. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00849-3 · Cited by 81
Li, Y., Sang, S., Ren, W., Pei, Y., Bian, Y., Chen, Y., & Sun, H. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113874 · Cited by 77
Azizi, S. A. (2020) · The Neuroscientist · doi:10.1177/1073858420974336 · Cited by 81
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Bodakuntla, S., Schnitzler, A., Villablanca, C., González-Billault, C. E., Bièche, I., Janke, C., & Magiera, M. M. (2020) · Journal of Cell Science · doi:10.1242/jcs.241802 · Cited by 73
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Huang, L., Peng, Y., Tao, X., Ding, X., Li, R., Jiang, Y., & Zuo, W. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1623181 · Cited by 64
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Fernandez-Valenzuela, J. J., Sanchez-Varo, R. M., Muñoz‐Castro, C., Castro, V. D., Sánchez‐Mejías, E., Navarro, V., Jiménez, S., Nuñez‐Diaz, C., Gómez-Arboledas, Á., Moreno‐González, I., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-71767-4 · Cited by 63
Fang, C., Hernandez, P., Liow, K. K., Damiano, E., Zetterberg, H., Blennow, K., Feng, D., Chen, M., & Maccecchini, M. L. (2022) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2022.84 · Cited by 66
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Radwitz, J., Hausrat, T. J., Heisler, F. F., Janiesch, P. C., Pechmann, Y., Rübhausen, M., & Kneussel, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04607-5 · Cited by 55
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Metadata
- Authors
- Guedes-Dias, P., & Holzbaur, E. L. F.
- Affiliations
- Technical University of Munich (DE)
- University of Pennsylvania (US)
- Corresponding author
- Holzbaur, Erika L. F.
- Venue
- Science
- Published
- 2019-10-11
- Volume
- 366
- Issue
- 6462
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC6996143
- OpenAlex
- W2979904465
- Cited by
- 355
- References
- 199
- Citations by year
- 2026: 43 · 2025: 65 · 2024: 61 · 2023: 43 · 2022: 63 · 2021: 44 · 2020: 31 · 2019: 3
- FWCI
- 4.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (R35 GM126950)
- Alexander von Humboldt-Stiftung
- Deutsche Forschungsgemeinschaft (EXC 2145 SyNergy)
- Elite Network Bavaria
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- axonal transport, kinesin motors, dynein motor, microtubules, vesicle trafficking, presynaptic terminals, synaptic function, synaptic transmission, growth factor transport, protein aggregation, learning and memory
- MeSH terms
- Animals, Axonal Transport, Humans, Microtubules, Protein Processing, Post-Translational, Synapses, Tubulin, Protein Isoforms, Mice
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