Myelin-, reactive glia-, and scar-derived CNS axon growth inhibitors: Expression, receptor signaling, and correlation with axon regeneration, Glia, vol.154, issue.3, pp.225-251, 2004. ,
DOI : 10.1002/glia.10315
Defeating inhibition of regeneration by scar and myelin components, Handb Clin Neurol, vol.109, pp.503-522, 2012. ,
DOI : 10.1016/B978-0-444-52137-8.00031-0
Central Nervous System Regenerative Failure: Role of Oligodendrocytes, Astrocytes, and Microglia, Cold Spring Harbor Perspectives in Biology, vol.7, issue.3, p.20602, 2015. ,
DOI : 10.1101/cshperspect.a020602
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355267
Macrophage Phenotype as a Determinant of Biologic Scaffold Remodeling, Tissue Engineering Part A, vol.14, issue.11, pp.1835-1842, 2008. ,
DOI : 10.1089/ten.tea.2007.0264
Macrophage phenotype as a predictor of constructive remodeling following the implantation of biologically derived surgical mesh materials, Acta Biomaterialia, vol.8, issue.3, pp.978-987, 2012. ,
DOI : 10.1016/j.actbio.2011.11.031
Robust CNS regeneration after complete spinal cord transection using aligned poly-l-lactic acid microfibers, Biomaterials, vol.32, issue.26, pp.6068-6079, 2011. ,
DOI : 10.1016/j.biomaterials.2011.05.006
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163047
Complete Spinal Cord Transection Treated by Implantation of a Reinforced Synthetic Hydrogel Channel Results in Syringomyelia and Caudal Migration of the Rostral Stump, Neurosurgery, vol.59, issue.1, pp.183-92, 2006. ,
DOI : 10.1227/01.NEU.0000219859.35349.EF
Long-lasting significant functional improvement in chronic severe spinal cord injury following scar resection and polyethylene glycol implantation, Neurobiology of Disease, vol.67, pp.165-179, 2014. ,
DOI : 10.1016/j.nbd.2014.03.018
Long-Distance Growth and Connectivity of Neural Stem Cells after Severe Spinal Cord Injury, Cell, vol.150, issue.6, pp.1264-1273, 2012. ,
DOI : 10.1016/j.cell.2012.08.020
Alginate hydrogel and matrigel as potential cell carriers for neurotransplantation, Journal of Biomedical Materials Research Part A, vol.161, issue.2, pp.242-252, 2006. ,
DOI : 10.1002/jbm.a.30603
Chitosan implants in the rat spinal cord: Biocompatibility and biodegradation, Journal of Biomedical Materials Research Part A, vol.23, issue.6, pp.395-404, 2011. ,
DOI : 10.1002/jbm.a.33070
The Use of Chitosan-Based Scaffolds to Enhance Regeneration in the Nervous System, Int Rev Neurobiol, vol.109, pp.1-62, 2013. ,
DOI : 10.1016/B978-0-12-420045-6.00001-8
Regenerative medicine for the treatment of spinal cord injury: more than just promises?, Journal of Cellular and Molecular Medicine, vol.88, issue.334, pp.2564-2582, 2012. ,
DOI : 10.1111/j.1582-4934.2012.01603.x
Chitin-based Materials in Tissue Engineering: Applications in Soft Tissue and Epithelial Organ, International Journal of Molecular Sciences, vol.9, issue.Suppl 1, pp.1936-1963, 2011. ,
DOI : 10.1016/j.biomaterials.2011.02.057
A material decoy of??biological media based on??chitosan physical hydrogels: application to??cartilage tissue engineering, Biochimie, vol.88, issue.5, pp.551-564, 2006. ,
DOI : 10.1016/j.biochi.2006.03.002
Multi-membrane chitosan hydrogels as chondrocytic cell bioreactors, Biomaterials, vol.32, issue.23, pp.5354-5364, 2011. ,
DOI : 10.1016/j.biomaterials.2011.04.012
URL : https://hal.archives-ouvertes.fr/hal-00649105
Repair of thoracic spinal cord injury by chitosan tube implantation in adult rats, Biomaterials, vol.30, issue.6, pp.1121-1132, 2009. ,
DOI : 10.1016/j.biomaterials.2008.10.063
Chitosan Channels Containing Spinal Cord-Derived Stem/Progenitor Cells for Repair of Subacute Spinal Cord Injury in the Rat, Neurosurgery, vol.67, issue.6, pp.1733-1744, 2010. ,
DOI : 10.1227/NEU.0b013e3181f9af35
NT3-chitosan elicits robust endogenous neurogenesis to enable functional recovery after spinal cord injury, Proceedings of the National Academy of Sciences, vol.49, issue.3, pp.13354-13359, 2015. ,
DOI : 10.1016/S0165-0270(99)00113-2
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629318
Chitosan scaffolds induce human dental pulp stem cells to neural differentiation: potential roles for spinal cord injury therapy, Cell and Tissue Research, vol.43, issue.1, 2016. ,
DOI : 10.1007/s00441-016-2402-1
Rheometric Study of the Gelation of Chitosan in Aqueous Solution without Cross-Linking Agent, Biomacromolecules, vol.6, issue.2, pp.653-662, 2005. ,
DOI : 10.1021/bm049593m
Determination of degree of deacetylation of chitosan by 1H NMR spectroscopy, Polymer Bulletin, vol.I, issue.1, pp.87-94, 1991. ,
DOI : 10.1007/BF00299352
Chitosan Hydrogels for the Regeneration of Infarcted Myocardium: Preparation, Physicochemical Characterization, and Biological Evaluation, Biomacromolecules, vol.17, issue.5, pp.1662-72, 2016. ,
DOI : 10.1021/acs.biomac.6b00075
URL : https://hal.archives-ouvertes.fr/hal-01396644
Chitosan hydrogel for repairing nerve tissue, p.2874672, 2016. ,
Salmon fibrin treatment of spinal cord injury promotes functional recovery and density of serotonergic innervation, Experimental Neurology, vol.235, issue.1, pp.345-356, 2012. ,
DOI : 10.1016/j.expneurol.2012.02.016
Improving Axial Resolution in Confocal Microscopy with New High Refractive Index Mounting Media, PLOS ONE, vol.43, issue.1 Suppl, p.121096, 2015. ,
DOI : 10.1371/journal.pone.0121096.t001
URL : https://hal.archives-ouvertes.fr/hal-01233480
A New Method of Study of the Brain Capillaries and its Application to the Regional Localisation of Mental Disorder, J Anat, vol.69, pp.62-71, 1934. ,
Giant scaffolding protein AHNAK1 interacts with ??-dystroglycan and controls motility and mechanical properties of schwann cells, Glia, vol.32, issue.Mar 27, pp.1392-1406, 2014. ,
DOI : 10.1002/glia.22685
Protein analysis on two-dimensional polyacrylamide gels in the femtogram range: Use of a new sulfur-labeling reagent, Analytical Biochemistry, vol.169, issue.2, pp.372-375, 1988. ,
DOI : 10.1016/0003-2697(88)90298-9
The Isolation and Characterization of Murine Macrophages, Curr Protoc Immunol Chapter, vol.35, 2008. ,
DOI : 10.1002/0471142735.im1401s83
A Sensitive and Reliable Locomotor Rating Scale for Open Field Testing in Rats, Journal of Neurotrauma, vol.12, issue.1, pp.1-21, 1995. ,
DOI : 10.1089/neu.1995.12.1
CatWalk-Assisted Gait Analysis in the Assessment of Spinal Cord Injury, Journal of Neurotrauma, vol.23, issue.3-4, pp.537-548, 2006. ,
DOI : 10.1089/neu.2006.23.537
Astrocytic and Vascular Remodeling in the Injured Adult Rat Spinal Cord after Chondroitinase ABC Treatment, Journal of Neurotrauma, vol.31, issue.9, pp.803-818, 2014. ,
DOI : 10.1089/neu.2013.3143
Extensive structural remodeling of the injured spinal cord revealed by phosphorylated MAP1B in sprouting axons and degenerating neurons, European Journal of Neuroscience, vol.20, issue.6, pp.1446-1461, 2007. ,
DOI : 10.1111/j.1460-9568.2007.05794.x
URL : https://hal.archives-ouvertes.fr/hal-00181436
Managing Inflammation after Spinal Cord Injury through Manipulation of Macrophage Function, Neural Plasticity, vol.172, issue.7, p.945034, 2013. ,
DOI : 10.1038/nrn3053
URL : http://doi.org/10.1155/2013/945034
Cytokine pathways regulating glial and leukocyte function after spinal cord and peripheral nerve injury, Experimental Neurology, vol.258, pp.62-77, 2014. ,
DOI : 10.1016/j.expneurol.2014.04.006
Inflammation and its role in neuroprotection, axonal regeneration and functional recovery after spinal cord injury, Experimental Neurology, vol.209, issue.2, pp.378-388, 2008. ,
DOI : 10.1016/j.expneurol.2007.06.009
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2692462
Emerging Concepts in Myeloid Cell Biology after Spinal Cord Injury, Neurotherapeutics, vol.20, issue.Pt 7, pp.252-261, 2011. ,
DOI : 10.1007/s13311-011-0032-6
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101835
Functional plasticity of macrophages: reversible adaptation to changing microenvironments, Journal of Leukocyte Biology, vol.76, issue.3, pp.509-513, 2004. ,
DOI : 10.1189/jlb.0504272
Sequential expression of macrophage anti-microbial/inflammatory and wound healing markers following innate, alternative and classical activation, Clinical & Experimental Immunology, vol.89, issue.3, pp.369-379, 2010. ,
DOI : 10.1111/j.1365-2249.2009.04086.x
Identification of Two Distinct Macrophage Subsets with Divergent Effects Causing either Neurotoxicity or Regeneration in the Injured Mouse Spinal Cord, Journal of Neuroscience, vol.29, issue.43, pp.13435-13444, 2009. ,
DOI : 10.1523/JNEUROSCI.3257-09.2009
Molecular and cellular mechanisms underlying the role of blood vessels in spinal cord injury and repair, Cell and Tissue Research, vol.94, issue.3, pp.269-288, 2012. ,
DOI : 10.1007/s00441-012-1440-6
Griffonia simplicifolia isolectin B4 identifies a specific subpopulation of angiogenic blood vessels following contusive spinal cord injury in the adult mouse, The Journal of Comparative Neurology, vol.21, issue.1, pp.1031-1052, 2008. ,
DOI : 10.1002/cne.21570
Temporal progression of angiogenesis and basal lamina deposition after contusive spinal cord injury in the adult rat, The Journal of Comparative Neurology, vol.78, issue.4, pp.308-324, 2002. ,
DOI : 10.1002/cne.10168
Micropatterned ECM substrates reveal complementary contribution of low and high affinity ligands to neurite outgrowth, Cytoskeleton, vol.127, issue.6 Pt 2, pp.373-388, 2011. ,
DOI : 10.1002/cm.20518
Adult NG2+ Cells Are Permissive to Neurite Outgrowth and Stabilize Sensory Axons during Macrophage-Induced Axonal Dieback after Spinal Cord Injury, Journal of Neuroscience, vol.30, issue.1, pp.255-265, 2010. ,
DOI : 10.1523/JNEUROSCI.3705-09.2010
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823089
Entrapment via Synaptic-Like Connections between NG2 Proteoglycan+ Cells and Dystrophic Axons in the Lesion Plays a Role in Regeneration Failure after Spinal Cord Injury, Journal of Neuroscience, vol.34, issue.49, pp.16369-16384, 2014. ,
DOI : 10.1523/JNEUROSCI.1309-14.2014
Spontaneous longitudinally orientated axonal regeneration is associated with the Schwann cell framework within the lesion site following spinal cord compression injury of the rat, Journal of Neuroscience Research, vol.53, issue.1, pp.51-65, 1998. ,
DOI : 10.1002/(SICI)1097-4547(19980701)53:1<51::AID-JNR6>3.0.CO;2-I
Automated Quantitative Gait Analysis During Overground Locomotion in the Rat: Its Application to Spinal Cord Contusion and Transection Injuries, Journal of Neurotrauma, vol.18, issue.2, pp.187-201, 2001. ,
DOI : 10.1089/08977150150502613
Molecular dissection of reactive astrogliosis and glial scar formation, Trends in Neurosciences, vol.32, issue.12, pp.638-647, 2009. ,
DOI : 10.1016/j.tins.2009.08.002
Astrocyte scar formation aids central nervous system axon regeneration, Nature, vol.34, issue.7598, pp.195-200, 2016. ,
DOI : 10.1038/nature17623
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243141
Glial Scar Borders Are Formed by Newly Proliferated, Elongated Astrocytes That Interact to Corral Inflammatory and Fibrotic Cells via STAT3-Dependent Mechanisms after Spinal Cord Injury, Journal of Neuroscience, vol.33, issue.31, pp.12870-12886, 2013. ,
DOI : 10.1523/JNEUROSCI.2121-13.2013
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728693
Regeneration beyond the glial scar, Nature Reviews Neuroscience, vol.5, issue.2, pp.146-156, 2004. ,
DOI : 10.1038/nrn1326
Guiding migration of transplanted glial progenitor cells in the injured spinal cord, Scientific Reports, vol.161, issue.1, p.22576, 2016. ,
DOI : 10.1016/S0079-6123(06)61027-3
The astrocyte/meningeal cell interface is a barrier to neurite outgrowth which can be overcome by manipulation of inhibitory molecules or axonal signalling pathways, Molecular and Cellular Neuroscience, vol.24, issue.4, pp.913-925, 2003. ,
DOI : 10.1016/j.mcn.2003.09.004
Changes in distribution, cell associations, and protein expression levels of NG2, neurocan, phosphacan, brevican, versican V2, and tenascin-C during acute to chronic maturation of spinal cord scar tissue, Journal of Neuroscience Research, vol.17, issue.3, pp.427-444, 2003. ,
DOI : 10.1002/jnr.10523
Axonal regeneration through regions of chondroitin sulfate proteoglycan deposition after spinal cord injury: a balance of permissiveness and inhibition, J Neurosci, vol.23, pp.9276-9288, 2003. ,
NG2 Colocalizes With Axons and Is Expressed by a Mixed Cell Population in Spinal Cord Lesions, Journal of Neuropathology and Experimental Neurology, vol.65, issue.4, pp.406-420, 2006. ,
DOI : 10.1097/01.jnen.0000218447.32320.52
The Curious Case of NG2 Cells: Transient Trend or Game Changer?, ASN Neuro, vol.135, issue.1, p.52, 2011. ,
DOI : 10.1038/nn1854
Can regenerating axons recapitulate developmental guidance during recovery from spinal cord injury?, Nature Reviews Neuroscience, vol.10, issue.8, pp.603-616, 2006. ,
DOI : 10.1038/nrn1957
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2288666
Repertoire of microglial and macrophage responses after spinal cord injury, Nature Reviews Neuroscience, vol.109, issue.7, pp.388-399, 2011. ,
DOI : 10.1038/nrn3053
Harnessing monocyte-derived macrophages to control central nervous system pathologies: no longer ???if??? but ???how???, The Journal of Pathology, vol.100, issue.Suppl 1, pp.332-346, 2013. ,
DOI : 10.1002/path.4106
Alternatively Activated Macrophages in Spinal Cord Injury and Remission: Another Mechanism for Repair?, Molecular Neurobiology, vol.265, issue.1???2, pp.1011-1019, 2013. ,
DOI : 10.1007/s12035-013-8398-6
Macrophage activation and its role in repair and pathology after spinal cord injury, Brain Research, vol.1619, pp.1-11, 2015. ,
DOI : 10.1016/j.brainres.2014.12.045
URL : http://doi.org/10.1016/j.brainres.2014.12.045
The significance of macrophage polarization subtypes for animal models of tissue fibrosis and human fibrotic diseases, Clinical and Translational Medicine, vol.110, issue.Suppl1, 2015. ,
DOI : 10.1186/s40169-015-0047-4
Cellular and molecular mechanisms of glial scarring and progressive cavitation: in vivo and in vitro analysis of inflammation-induced secondary injury after CNS trauma, J Neurosci, vol.19, pp.8182-8198, 1999. ,
Another Barrier to Regeneration in the CNS: Activated Macrophages Induce Extensive Retraction of Dystrophic Axons through Direct Physical Interactions, Journal of Neuroscience, vol.28, issue.38, pp.9330-9341, 2008. ,
DOI : 10.1523/JNEUROSCI.2488-08.2008
Exploring the full spectrum of macrophage activation, Nature Reviews Immunology, vol.117, issue.12, pp.958-969, 2008. ,
DOI : 10.1038/nri2448
The phenotype of murine wound macrophages, Journal of Leukocyte Biology, vol.87, issue.1, pp.59-67, 2010. ,
DOI : 10.1189/jlb.0409236
Macrophage polarization following chitosan implantation, Biomaterials, vol.34, issue.38, pp.9952-9959, 2013. ,
DOI : 10.1016/j.biomaterials.2013.09.012