Cited by 606Nerve injury and regenerationNeurogenesis and neuroplasticity mechanismsSpinal Cord Injury Research

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Robust regeneration of adult sensory axons in degenerating white matter of the adult rat spinal cord.

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Davies, Stephen J. A., Goucher, David R., Doller, Catherine, Silver, Jerry·1999·The Journal of Neuroscience

DOI 10.1523/jneurosci.19-14-05810.1999PMC PMC6783087

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Abstract

We have recently reported that minimally disturbed adult CNS white matter can support regeneration of adult axons by using a novel microtransplantation technique to inject minute volumes of dissociated adult rat dorsal root ganglion neurons directly into adult rat CNS pathways (Davies et al., 1997). This atraumatic injection procedure minimized scarring and allowed considerable numbers of regenerating adult axons immediate access to the adult CNS glial terrain where they rapidly extended for long distances. A critical question remained as to whether degenerating white matter at acute and chronic stages (up to 3 months) after injury could still support regeneration. To investigate this, we have microtransplanted adult sensory neurons into degenerating white matter of the adult rat spinal cord several millimeters rostral to a severe lesion of the dorsal columns. Regeneration of donor sensory axons in both directions away from the site of transplantation was robust even within white matter undergoing fulminant Wallerian degeneration despite intimate contact with myelin. Along their route, the regrowing axons extended large numbers of collaterals into the adjacent dorsal horn. However, after entering the lesion, the rapidly extending growth cones stopped and became dystrophic within high concentrations of reactive glial matrix. Our results offer compelling evidence that the major environmental impediment to regeneration in the adult CNS is the molecular barrier that forms directly at the lesion site, and that degenerating white matter beyond the glial scar has a far greater intrinsic ability to support axon regeneration than previously thought possible.

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Degeneration and Regeneration of the Nervous System.
(1929) · JAMA · doi:10.1001/jama.1929.02710220063037 · Cited by 2,908
‘Green mice’ as a source of ubiquitous green cells
Okabe, M., Ikawa, M., Kominami, K., Nakanishi, T., & Nishimune, Y. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)00313-x · Cited by 2,581
Axonal Elongation into Peripheral Nervous System "Bridges" After Central Nervous System Injury in Adult Rats
David, S., & Aguayo, A. J. (1981) · Science · doi:10.1126/science.6171034 · Cited by 1,698
Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhibitory molecules on reactive astrocytes
McKeon, R., Schreiber, R., Rudge, J., & Silver, J. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-11-03398.1991 · Cited by 1,188
Self-citation
Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth
McKerracher, L. J., David, S., Jackson, D. L., Kottis, V., Dunn, R. J., & Braun, P. E. (1994) · Neuron · doi:10.1016/0896-6273(94)90247-x · Cited by 1,125
Microglia: Intrinsic immuneffector cell of the brain
Gehrmann, J., Matsumoto, Y., & Kreutzberg, G. W. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00015-h · Cited by 1,111
Neuronal and Glial Apoptosis after Traumatic Spinal Cord Injury
Liu, X. Z., Xu, X. M., Hu, R., Du, C., Zhang, S. X., McDonald, J. W., Dong, H. X., Wu, Y. J., Fan, G. S., Jacquin, M. F., et al. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-14-05395.1997 · Cited by 770
Regeneration of adult axons in white matter tracts of the central nervous system
Davies, S. J. A., Fitch, M. T., Memberg, S. P., Hall, A. K., Raisman, G., & Silver, J. (1997) · Nature · doi:10.1038/37776 · Cited by 737
Self-citation
Inhibitors of Neurite Growth
Schwab, M. E., Kapfhammer, J. P., & Bandtlow, C. E. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.003025 · Cited by 539
Prior Exposure to Neurotrophins Blocks Inhibition of Axonal Regeneration by MAG and Myelin via a cAMP-Dependent Mechanism
Cai, D., Shen, Y.-J., de Bellard, M. E., Tang, S., & Filbin, M. T. (1999) · Neuron · doi:10.1016/s0896-6273(00)80681-9 · Cited by 536

Show all 54 references

Research works printed but not linked: 2

Huber, 1998, Developmental expression pattern and functional analysis of NOGO (formerly NI-35/250), a major inhibitor of CNS regeneration., Soc Neurosci Abstr, 24, 616.6
McKeon, 1997, Gene expression in glial scars following CNS injury., Soc Neurosci Abstr, 23, 777.1

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Authors: Davies, S. J. A., Goucher, D. R., Doller, C., & Silver, J.
Affiliations: Case Western Reserve University (US)
ORCID: Davies, Stephen J. A.
Silver, Jerry
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 1999-07-15
Volume: 19
Issue: 14
Pages: 5810-5822
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.19-14-05810.1999
PMC: PMC6783087
OpenAlex: W1826719783
Cited by: 606
References: 54
Citations by year: 2026: 2 · 2025: 6 · 2024: 5 · 2023: 7 · 2022: 11 · 2021: 13 · 2020: 9 · 2019: 11 · 2018: 13 · 2017: 13 · 2016: 13 · 2015: 13 · 2014: 27 · 2013: 22 · 2012: 39
FWCI: 14.12
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 184 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Neurological Disorders and Stroke (NS 25713)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Health Sciences › Medicine › Clinical Neurology › Spinal Cord Injury Research
Keywords: axon regeneration, spinal cord injury, dorsal root ganglion neurons, microtransplantation, Wallerian degeneration, glial scar, sensory axons, dorsal horn, myelin, dorsal column lesion
MeSH terms: Animals, Astrocytes, Axons, Cells, Cultured, Chickens, Ganglia, Spinal, Luminescent Proteins, Mice, Inbred C57BL, Mice, Transgenic, Myelin Sheath, Nerve Degeneration, Nerve Regeneration, Neurons, Neurons, Afferent, Oligodendroglia, Spinal Cord, Time Factors, Rats, Sprague-Dawley, Coculture Techniques, Green Fluorescent Proteins, Mice, Rats

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Robust regeneration of adult sensory axons in degenerating white matter of the adult rat spinal cord.

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