The DOI matches its Crossref record; 122 of the 122 references it cites were found in a registry or an index.
Axon degeneration mechanisms: commonality amid diversity
Abstract
A wide range of insults can trigger axon degeneration, and axons respond with diverse morphology, topology and speed. However, recent genetic, immunochemical, morphological and pharmacological investigations point to convergent degeneration mechanisms. The principal convergence points - poor axonal transport, mitochondrial dysfunction and an increase in intra-axonal calcium - have been identified by rescuing axons with the slow Wallerian degeneration gene (Wld(S)) and studies with blockers of sodium or calcium influx. By understanding how the pathways fit together, we can combine our knowledge of mechanisms, and potentially also treatment strategies, from different axonal disorders.
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“Another important factor might be the disruption of fast axonal transport, resulting in focal swellings filled with various organelles, as seen in the vicinity but also distant from plaques in several AD transgenic models [27,28,29,30], resembling Wallerian degeneration [31].”
From Neuron Loss in Alzheimer’s Disease: Translation in Transgenic Mouse Models (2020) · cites this paper as [31]
In the citing paper
“The principal mechanisms of axon degeneration are metabolic stress, disturbed axonal transport, and mitochondrial dysfunction [301].”
From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [301]
Citations
Cites
Alzheimer's Disease Is a Synaptic Failure
Selkoe, D. J. (2002) · Science · doi:10.1126/science.1074069 · Cited by 4,420
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029
Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP
Feng, G., Mellor, R. H., Bernstein, M., Keller-Peck, C., Nguyen, Q. T., Wallace, M., Nerbonne, J. M., Lichtman, J. W., & Sanes, J. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00084-2 · Cited by 3,042
Axonal damage in acute multiple sclerosis lesions
Ferguson, B. (1997) · Brain · doi:10.1093/brain/120.3.393 · Cited by 1,532
Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man
Fischer, L. R., Culver, D. G., Tennant, P., Davis, A. A., Wang, M.-S., Castellano-Sanchez, A. A., Khan, J., Polak, M. A., & Glass, J. D. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2003.10.004 · Cited by 1,383
Death by design: apoptosis, necrosis and autophagy
Edinger, A. L., & Thompson, C. B. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.09.011 · Cited by 1,362
Axonopathy and Transport Deficits Early in the Pathogenesis of Alzheimer’s Disease
Stokin, G. B., Lillo, C., Falzone, T. L., Brusch, R. G., Rockenstein, E., Mount, S. L., Raman, R., Davies, P., Masliah, E., Williams, D. S., et al. (2005) · Science · doi:10.1126/science.1105681 · Cited by 1,214
Increased Nuclear NAD Biosynthesis and SIRT1 Activation Prevent Axonal Degeneration
Araki, T., Sasaki, Y., & Milbrandt, J. (2004) · Science · doi:10.1126/science.1098014 · Cited by 1,060
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination
Lappe-Siefke, C., Goebbels, S., Gravel, M., Nicksch, E., Lee, J., Braun, P. E., Griffiths, I. R., & Nave, K.-A. (2003) · Nature Genetics · doi:10.1038/ng1095 · Cited by 1,036
Erythropoietin prevents neuronal apoptosis after cerebral ischemia and metabolic stress
Sirén, A., Fratelli, M., Brines, M. L., Goemans, C. G., Casagrande, S., Lewczuk, P., Keenan, S., Gleiter, C. H., Pasquali, C., Capobianco, A., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051606598 · Cited by 1,019
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- Wishart, T. M. et al. Transcriptional regulation of pituitary tumour transforming gene-1 by the neuroprotective WldS gene in mouse cerebellar granule cells and HEK293 cell lines. J. Physiol. 565P, C74 (2004).
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Gómez, F. J., Aguirre, P., González-Billault, C. E., & Núñez, M. T. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-010-0489-1 · Cited by 18
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Yang, B., Qu, M., Wang, R., Chatterton, J. E., Liu, X., Zhu, B., Narisawa, S., Millán, J. L., Nakanishi, N., Swoboda, K. J., et al. (2015) · eLife · doi:10.7554/elife.06500 · Cited by 17
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Gómez-Deza, J., Nebiyou, M., Alkaslasi, M. R., Nadal-Nicolás, F. M., Somasundaram, P., Slavutsky, A. L., Li, W., Ward, M. E., Watkins, T. A., & Pichon, C. E. L. (2024) · Nature Communications · doi:10.1038/s41467-024-54982-9 · Cited by 16
Fyfe, J. C., Al-Temaimi, R. A., Castellani, R. J., Rosenstein, D. S., Goldowitz, D., & Henthorn, P. S. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22423 · Cited by 16
Fujiwara, T., & Morimoto, K. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.06.071 · Cited by 16
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Shin, J. E., Ha, H., Cho, E. H., Kim, Y. K., & Cho, Y. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24404 · Cited by 16
Chi, Z., Adini, A., Birsner, A. E., Bazinet, L. F., Akula, J. D., & D’Amato, R. J. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.12.029 · Cited by 16
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Kincses, Z. T., Hořínek, D., Szabó, N., Tóth, E. M., Csete, G., Buksakowska, I., Hort, J., & Vécsei, L. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-122431 · Cited by 16
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Sou, Y., Kakuta, S., Kamikubo, Y., Niisato, K., Sakurai, T., Parajuli, L. K., Tanida, I., Saito, H., 昇, 鈴., Sakimura, K., et al. (2019) · eNeuro · doi:10.1523/eneuro.0427-18.2019 · Cited by 16
Rose, F. F., Meehan, P. W., Coady, T. H., Garcia, V. B., Garcia, M. L., & Lorson, C. L. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.07.130 · Cited by 16
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Pope, H. M., & Voigt, M. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0103283 · Cited by 14
Uemura, M., & Ishiguro, H. (2015) · Cryobiology · doi:10.1016/j.cryobiol.2015.01.006 · Cited by 14
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Katow, H., Kanaya, T., Ogawa, T., Egawa, R., & Yawo, H. (2017) · Development Growth & Differentiation · doi:10.1111/dgd.12346 · Cited by 11
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Audouard, E., Hees, L. V., Suain, V., Yilmaz, Z., Poncelet, L., Leroy, K., & Brion, J. (2015) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.06.011 · Cited by 11
Koh, C., Tang, P., Chen, H., Hsu, Y., Hsieh, C., & Tseng, W. I. (2018) · Neurorehabilitation and neural repair · doi:10.1177/1545968318779730 · Cited by 14
Pottorf, T. S., Mann, A., Fross, S., Mansel, C. O., & Vohra, B. P. S. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2018.09.010 · Cited by 11
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Lavado, A., Guo, X., Smith, A. S. T., Akanda, N., Martin, C., Cai, Y., Elbrecht, D., Tran, M., Bryant, J.-P., Colón, A., et al. (2017) · PubMed · Cited by 11
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Edgar, J. M., & Griffiths, I. R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-396460-1.00007-x · Cited by 13
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Subramanian, R. G., Zivadinov, R., Bergsland, N., Dwyer, M. G., Weinstock‐Guttman, B., & Jakimovski, D. (2023) · Journal of Neurology · doi:10.1007/s00415-023-11709-y · Cited by 10
Luis Cartier, R., Carmen Vergara, R., & María Antonieta Valenzuela, P. (2007) · Revista médica de Chile · doi:10.4067/s0034-98872007000900007 · Cited by 10
Munter, S. D., Bamps, D., Malheiro, A. R., Baboota, R. K., Brites, P., & Baes, M. I. (2018) · Brain Pathology · doi:10.1111/bpa.12586 · Cited by 10
Subaraja, M., & Vanisree, A. J. (2019) · Environmental Science and Pollution Research · doi:10.1007/s11356-019-04740-y · Cited by 10
NAD+-dependent mechanism of pathological axon degeneration
Cao, Y., Wang, Y., & Yang, J. H. (2022) · Cell Insight · doi:10.1016/j.cellin.2022.100019 · Cited by 10
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Kunik, D., Dion, C., Ozaki, T., Levin, L. A., & Costantino, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026832 · Cited by 10
Kincses, Z. T., Király, A., Veréb, D., & Vécsei, L. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-143195 · Cited by 10
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Zhu, Q., Lin, M., Bi, S., Ni, Z., Zhao, J., Chen, B., Fan, G., & Shang, X. (2016) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000447056 · Cited by 10
Gallese, V. (2013) · Vandenhoeck & Ruprecht eBooks · doi:10.13109/9783666451300.75 · Cited by 10
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Metadata
- Authors
- Coleman, M.
- Affiliations
- Babraham Institute (GB)
- Corresponding author
- Coleman, Michael
- ORCID
- Coleman, Michael
- Venue
- Nature reviews. Neuroscience
- Published
- 2005-10-14
- Volume
- 6
- Issue
- 11
- Pages
- 889-898
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2042991032
- Cited by
- 819
- References
- 122
- Citations by year
- 2026: 15 · 2025: 30 · 2024: 13 · 2023: 22 · 2022: 18 · 2021: 35 · 2020: 40 · 2019: 32 · 2018: 40 · 2017: 48 · 2016: 43 · 2015: 51 · 2014: 47 · 2013: 58 · 2012: 53
- FWCI
- 2.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Biotechnology and Biological Sciences Research Council
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- axonal degeneration, Wallerian degeneration, axonal transport, mitochondrial dysfunction, intracellular calcium, sodium influx, calcium influx
- MeSH terms
- Animals, Axons, Axonal Transport, Central Nervous System, Humans, Nerve Tissue Proteins, Wallerian Degeneration
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