Therapeutic administration of mouse mast cell protease 6 improves functional recovery after traumatic spinal cord injury in mice by promoting remyelination and reducing glial scar formation

Author:

Vangansewinkel Tim12,Lemmens Stefanie3,Tiane Assia456,Geurts Nathalie3,Dooley Dearbhaile78,Vanmierlo Tim456,Pejler Gunnar9,Hendrix Sven10ORCID

Affiliation:

1. Cardio and Organ Systems Biomedical Research Institute, Hasselt University Diepenbeek Belgium

2. VIB, Center for Brain & Disease Research, Laboratory of Neurobiology Leuven Belgium

3. Department of Immunology and Infection Biomedical Research Institute, Hasselt University Diepenbeek Belgium

4. Department of Neuroscience, Faculty of Medicine and Life Sciences Biomedical Research Institute, Hasselt University Hasselt Belgium

5. Department Psychiatry and Neuropsychology, School for Mental Health and Neuroscience Maastricht University Maastricht The Netherlands

6. University MS Center (UMSC) Hasselt‐Pelt Hasselt Belgium

7. School of Medicine Health Sciences Centre, University College Dublin Belfield Ireland

8. UCD Conway Institute of Biomolecular & Biomedical Research University College Dublin Belfield Ireland

9. Department of Medical Biochemistry and Microbiology Uppsala University Uppsala Sweden

10. Institute for Translational Medicine Medical School Hamburg Hamburg Germany

Abstract

AbstractTraumatic spinal cord injury (SCI) most often leads to permanent paralysis due to the inability of axons to regenerate in the adult mammalian central nervous system (CNS). In the past, we have shown that mast cells (MCs) improve the functional outcome after SCI by suppressing scar tissue formation at the lesion site via mouse mast cell protease 6 (mMCP6). In this study, we investigated whether recombinant mMCP6 can be used therapeutically to improve the functional outcome after SCI. Therefore, we applied mMCP6 locally via an intrathecal catheter in the subacute phase after a spinal cord hemisection injury in mice. Our findings showed that hind limb motor function was significantly improved in mice that received recombinant mMCP6 compared with the vehicle‐treated group. In contrast to our previous findings in mMCP6 knockout mice, the lesion size and expression levels of the scar components fibronectin, laminin, and axon‐growth‐inhibitory chondroitin sulfate proteoglycans were not affected by the treatment with recombinant mMCP6. Surprisingly, no difference in infiltration of CD4+ T cells and reactivity of Iba‐1+ microglia/macrophages at the lesion site was observed between the mMCP6‐treated mice and control mice. Additionally, local protein levels of the pro‐ and anti‐inflammatory mediators IL‐1β, IL‐2, IL‐4, IL‐6, IL‐10, TNF‐α, IFNγ, and MCP‐1 were comparable between the two treatment groups, indicating that locally applied mMCP6 did not affect inflammatory processes after injury. However, the increase in locomotor performance in mMCP6‐treated mice was accompanied by reduced demyelination and astrogliosis in the perilesional area after SCI. Consistently, we found that TNF‐α/IL‐1β‐astrocyte activation was decreased and that oligodendrocyte precursor cell (OPC) differentiation was increased after recombinant mMCP6 treatment in vitro. Mechanistically, this suggests effects of mMCP6 on reducing astrogliosis and improving (re)myelination in the spinal cord after injury. In conclusion, these data show for the first time that recombinant mMCP6 is therapeutically active in enhancing recovery after SCI.

Funder

Agentschap voor Innovatie door Wetenschap en Technologie

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

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