Cited by 199Spinal Cord Injury ResearchNerve injury and regenerationTraumatic Brain Injury and Neurovascular Disturbances

Hematogenous macrophage depletion reduces the fibrotic scar and increases axonal growth after spinal cord injury.

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Zhu, Y., Soderblom, C., Krishnan, V., Ashbaugh, J., Bethea, J.R., Lee, J.K.·2015·Neurobiology of Disease

Abstract

Spinal cord injury (SCI) leads to formation of a fibrotic scar that is inhibitory to axon regeneration. Recent evidence indicates that the fibrotic scar is formed by perivascular fibroblasts, but the mechanism by which they are recruited to the injury site is unknown. Using bone marrow transplantation in mouse model of spinal cord injury, we show that fibroblasts in the fibrotic scar are associated with hematogenous macrophages rather than microglia, which are limited to the surrounding astroglial scar. Depletion of hematogenous macrophages results in reduced fibroblast density and basal lamina formation that is associated with increased axonal growth in the fibrotic scar. Cytokine gene expression analysis after macrophage depletion indicates that decreased Tnfsf8, Tnfsf13 (tumor necrosis factor superfamily members) and increased BMP1-7 (bone morphogenetic proteins) expression may serve as anti-fibrotic mechanisms. Our study demonstrates that hematogenous macrophages are necessary for fibrotic scar formation and macrophage depletion results in changes in multiple cytokines that make the injury site less fibrotic and more conducive to axonal growth.

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Crossref · 10.1016/j.nbd.2014.10.024

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  • In both MCAO and SCI models, macrophages are observed in the fibrotic scar and may associate with fibroblasts, and CD11b+ macrophages are partially responsible for recruitment of fibroblasts to the fibrotic scar following SCI.

    “In both MCAO and SCI models, macrophages are observed in the fibrotic scar and may associate with fibroblasts”

    From Living on the Edge of the CNS: Meninges Cell Diversity in Health and Disease (2021) · cites this paper as Zhu et al., 2015

  • Depletion of macrophages prior to SCI leads to depletion of pro-fibrotic cytokines, such as Tnfsf8 and Tnfsf13.

    “depletion of macrophages prior to SCI leads to depletion of pro-fibrotic cytokines, such as tumor necrosis factor superfamily members Tnfsf8 and Tnfsf13”

    From Living on the Edge of the CNS: Meninges Cell Diversity in Health and Disease (2021) · cites this paper as Zhu et al., 2015

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Authors
Zhu, Y., Soderblom, C., Krishnan, V., Ashbaugh, J., Bethea, J. R., & Lee, J. K.
Affiliations
University of Miami (US)
Corresponding author
Lee, J.K.
Venue
Neurobiology of Disease
Publisher
Elsevier BV
Published
2015-02
Volume
74
Pages
114-125
ISSN
0969-9961 (ISSN-L)
OpenAlex
W2080371301
Cited by
199
References
45
Citations by year
2026: 9 · 2025: 16 · 2024: 28 · 2023: 18 · 2022: 24 · 2021: 33 · 2020: 17 · 2019: 14 · 2018: 18 · 2017: 12 · 2016: 9
FWCI
5.20
Type
journal article
Language
en
Open access
Locations
  • Neurobiology of Disease (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • NINDS (R01NS081040, R21NS082835)
  • U.S. Army (W81XWH131007715)
  • The Miami Project to Cure Paralysis
  • the Buoniconti Fund
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Spinal Cord Injury Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
  • Health Sciences › Medicine › Neurology › Traumatic Brain Injury and Neurovascular Disturbances
Keywords
spinal cord injury, macrophage depletion, fibrotic scar, axon regeneration, perivascular fibroblasts, bone marrow transplantation, basement membrane, tumor necrosis factor superfamily, cytokine expression, antifibrotic mechanism
MeSH terms
Animals, Axons, Basement Membrane, Cicatrix, Disease Models, Animal, Female, Fibroblasts, Macrophages, Mice, Inbred C57BL, Mice, Transgenic, Nerve Regeneration, Spinal Cord Injuries, Bone Marrow Transplantation, Bone Morphogenetic Proteins, CD30 Ligand, Tumor Necrosis Factor Ligand Superfamily Member 13

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