Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury

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 or...

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Main Authors: Vincent Escarrat, Jimena Perez-Sanchez, Bilal El-Waly, Jorge E. Collazos-Castro, Franck Debarbieux
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/12/6/839
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author Vincent Escarrat
Jimena Perez-Sanchez
Bilal El-Waly
Jorge E. Collazos-Castro
Franck Debarbieux
author_facet Vincent Escarrat
Jimena Perez-Sanchez
Bilal El-Waly
Jorge E. Collazos-Castro
Franck Debarbieux
author_sort Vincent Escarrat
collection DOAJ
description 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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spelling doaj.art-1e435833429647a0bee915455210667a2023-11-17T10:12:34ZengMDPI AGCells2073-44092023-03-0112683910.3390/cells12060839Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord InjuryVincent Escarrat0Jimena Perez-Sanchez1Bilal El-Waly2Jorge E. Collazos-Castro3Franck Debarbieux4Institut des Neurosciences de la Timone, Aix-Marseille Université and CNRS UMR7289, 13005 Marseille, FranceInstitut des Neurosciences de la Timone, Aix-Marseille Université and CNRS UMR7289, 13005 Marseille, FranceInstitut des Neurosciences de la Timone, Aix-Marseille Université and CNRS UMR7289, 13005 Marseille, FranceNeural Repair and Biomaterials Laboratory, Hospital Nacional de Parapléjicos (SESCAM), 45071 Toledo, SpainInstitut des Neurosciences de la Timone, Aix-Marseille Université and CNRS UMR7289, 13005 Marseille, FrancePoor 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.https://www.mdpi.com/2073-4409/12/6/839two-photon microscopytransgenic fluorescent micebiocompatibilityneuroinflammationspinal cord injurynatural materials
spellingShingle Vincent Escarrat
Jimena Perez-Sanchez
Bilal El-Waly
Jorge E. Collazos-Castro
Franck Debarbieux
Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
Cells
two-photon microscopy
transgenic fluorescent mice
biocompatibility
neuroinflammation
spinal cord injury
natural materials
title Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
title_full Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
title_fullStr Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
title_full_unstemmed Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
title_short Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
title_sort composite fibrin and carbon microfibre implant to modulate postraumatic inflammation after spinal cord injury
topic two-photon microscopy
transgenic fluorescent mice
biocompatibility
neuroinflammation
spinal cord injury
natural materials
url https://www.mdpi.com/2073-4409/12/6/839
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