Journal
CELLS
Volume 12, Issue 6, Pages -Publisher
MDPI
DOI: 10.3390/cells12060839
Keywords
two-photon microscopy; transgenic fluorescent mice; biocompatibility; neuroinflammation; spinal cord injury; natural materials
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Poor functional recovery after spinal cord injury (SCI) has prompted the development of novel strategies. Our recent study demonstrated the immunomodulatory and pro-regenerative effects of bio-functionalized carbon microfibres (MFs) in a rat model of SCI. To enhance tissue repair and ease MF implantation, we developed a composite implant consisting of MFs embedded within a fibrin hydrogel. Our findings showed that the inclusion of MFs in the hydrogel inhibited fibrin degradation, promoted early recruitment of immune cells, and facilitated axonal regeneration over a 3-month period.
Poor functional recovery after spinal cord injury (SCI) drives the development of novel strategies to manage this devastating condition. We recently showed promising immunomodulatory and pro-regenerative actions of bio-functionalized carbon microfibres (MFs) implanted in a rodent model of SCI. In order to maximize tissue repair while easing MF implantation, we produced a composite implant based on the embedding of several MFs within a fibrin hydrogel. We used intravital imaging of fluorescent reporter mice at the early stages and spinal sections of the same animals 3 months later to characterize the neuroinflammatory response to the implant and its impact on axonal regeneration. Whereas fibrin alone was inert in the first week, its enzymatic degradation drove the chronic activation of microglial cells and axonal degeneration within 3 months. However, the presence of MFs inside the fibrin hydrogel slowed down fibrin degradation and boosted the early recruitment of immune cells. Noteworthy, there was an enhanced contribution of monocyte-derived dendritic cells (moDCs), preceding a faster transition toward an anti-inflammatory environment with increased axonal regeneration over 3 months. The inclusion of MF here ensured the long-term biocompatibility of fibrin hydrogels, which would otherwise preclude successful spinal cord regeneration.
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