[1]
National Spinal Cord Injury Statistical Center. Spinal cord injury facts and figures at a glance.
The Journal of Spinal Cord Medicine , 2010, 33(4): 439–440
[2] Sekhon L H, Fehlings M G. Epidemiology, demographics, and pathophysiology of acute spinal cord injury.
Spine , 2001, 26(24 Suppl): S2–S12
[3] Parr A M, Tator C H, Keating A. Bone marrow-derived mesenchymal stromal cells for the repair of central nervous system injury.
Bone Marrow Transplantation , 2007, 40(7): 609–619
[4] LaPlaca M C, Simon C M, Prado G R,
. CNS injury biomechanics and experimental models. In: Weber J T, Maas A I R, eds.
Neurotrauma: New Insights into Pathology and Treatment. Elsevier Science , 2007, 13-26
[5] Beattie M S, Hermann G E, Rogers R C,
. Cell death in models of spinal cord injury. In: McKerracher L, Doucet G, Rossignol S, eds.
Spinal Cord Trauma: Regeneration, Neural Repair and Functional Recovery .
Amsterdam:
Elsevier Science, 2002, 37–47
[6] Sauaia A, Moore F A, Moore E E,
. Epidemiology of trauma deaths: a reassessment.
The Journal of Trauma Injury Infection and Critical Care , 1995, 38(2): 185–193
[7] Tator C H. Update on the pathophysiology and pathology of acute spinal cord injury.
Brain Pathology , 1995, 5(4): 407–413
[8] Tator C H, Fehlings M G. Review of the secondary injury theory of acute spinal cord trauma with emphasis on vascular mechanisms.
Journal of Neurosurgery , 1991, 75(1): 15–26
[9] Guth L, Zhang Z Y, Steward O. The unique histopathological responses of the injured spinal cord - Implications for neuroprotective therapy. In: Trembly B S W, ed.
Neuroprotective Agents: Fourth International Conference , 1999, 366–384
[10] Yiu G, He Z. Glial inhibition of CNS axon regeneration.
Nature Reviews Neuroscience , 2006, 7(8): 617–627
[11] Profyris C, Cheema S S, Zang D W,
. Degenerative and regenerative mechanisms governing spinal cord injury.
Neurobiology of Disease , 2004, 15(3): 415–436
[12] Yiu G, He Z G. Glial inhibition of CNS axon regeneration.
Nature Reviews Neuroscience , 2006, 7(8): 617–627
[13] Fawcett J W, Asher R A. The glial scar and central nervous system repair.
Brain Research Bulletin , 1999, 49(6): 377–391
[14] Silver J, Miller J H. Regeneration beyond the glial scar.
Nature Reviews Neuroscience , 2004, 5(2): 146–156
[15] Tang X F, Davies J E, Davies S J A. 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 , 2003, 71(3): 427–444
[16] Hynds D L, Snow D M. Neurite outgrowth inhibition by chondroitin sulfate proteoglycan: stalling/stopping exceeds turning in human neuroblastoma growth cones.
Experimental Neurology , 1999, 160(1): 244–255
[17] Davies S J A, Goucher D R, Doller C,
. Robust regeneration of adult sensory axons in degenerating white matter of the adult rat spinal cord.
The Journal of Neuroscience , 1999, 19(14): 5810–5822
[18] Pasterkamp R J, Giger R J, Ruitenberg M J,
. Expression of the gene encoding the chemorepellent semaphorin III is induced in the fibroblast component of neural scar tissue formed following injuries of adult but not neonatal CNS.
Molecular and Cellular Neurosciences , 1999, 13(2): 143–166
[19] De Winter F, Oudega M, Lankhorst A J,
. Injury-induced class 3 semaphorin expression in the rat spinal cord.
Experimental Neurology , 2002, 175(1): 61–75
[20] Chen M S, Huber A B, van der Haar M E,
. Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1.
Nature , 2000, 403(6768): 434–439
[21] GrandPré T, Nakamura F, Vartanian T,
. Identification of the Nogo inhibitor of axon regeneration as a Reticulon protein.
Nature , 2000, 403(6768): 439–444
[22] Prinjha R, Moore S E, Vinson M,
. Neurobiology: Inhibitor of neurite outgrowth in humans.
Nature , 2000, 403(6768): 383–384
[23] Huber A B, Weinmann O, Br?samle C,
. Patterns of Nogo mRNA and protein expression in the developing and adult rat and after CNS lesions.
The Journal of Neuroscience , 2002, 22(9): 3553–3567
[24] Wang X X, Chun S J, Treloar H,
. Localization of Nogo-A and Nogo-66 receptor proteins at sites of axon-myelin and synaptic contact.
The Journal of Neuroscience , 2002, 22(13): 5505–5515
[25] McKerracher L, David S, Jackson D L,
. Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth.
Neuron , 1994, 13(4): 805–811
[26] Filbin M T. Myelin-associated inhibitors of axonal regeneration in the adult mammalian CNS.
Nature Reviews Neuroscience , 2003, 4(9): 703–713
[27] Kim J E, Li S X, GrandPré T,
. Axon regeneration in young adult mice lacking Nogo-A/B.
Neuron , 2003, 38(2): 187–199
[28] GrandPré T, Li S X, Strittmatter S M. Nogo-66 receptor antagonist peptide promotes axonal regeneration.
Nature , 2002, 417(6888): 547–551
[29] Simonen M, Pedersen V, Weinmann O,
. Systemic deletion of the myelin-associated outgrowth inhibitor Nogo-A improves regenerative and plastic responses after spinal cord injury.
Neuron , 2003, 38(2): 201–211
[30] Crowe M J, Bresnahan J C, Shuman S L,
. Apoptosis and delayed degeneration after spinal cord injury in rats and monkeys.
Nature Medicine , 1997, 3(1): 73–76
[31] Barres B A, Schmid R, Sendnter M,
. Multiple extracellular signals are required for long-term oligodendrocyte survival.
Development , 1993, 118(1): 283–295
[32] Takano R, Hisahara S, Namikawa K,
. Nerve growth factor protects oligodendrocytes from tumor necrosis factor-α-induced injury through Akt-mediated signaling mechanisms.
The Journal of Biological Chemistry , 2000, 275(21): 16360–16365
[33] Vartanian T, Goodearl A, Vieh?ver A,
. Axonal neuregulin signals cells of the oligodendrocyte lineage through activation of HER4 and Schwann cells through HER2 and HER3.
The Journal of Cell Biology , 1997, 137(1): 211–220
[34] Flores A I, Mallon B S, Matsui T,
. Akt-mediated survival of oligodendrocytes induced by neuregulins.
The Journal of Neuroscience , 2000, 20(20): 7622–7630
[35] Casaccia-Bonnefil P. Cell death in the oligodendrocyte lineage: a molecular perspective of life/death decisions in development and disease.
Glia , 2000, 29(2): 124–135
[36] Woerly S, Petrov P, Syková E,
. Neural tissue formation within porous hydrogels implanted in brain and spinal cord lesions: ultrastructural, immunohistochemical, and diffusion studies.
Tissue Engineering , 1999, 5(5): 467–488
[37] Engler A J, Sen S, Sweeney H L,
. Matrix elasticity directs stem cell lineage specification.
Cell , 2006, 126(4): 677–689
[38] Leipzig N D, Shoichet M S. The effect of substrate stiffness on adult neural stem cell behavior.
Biomaterials , 2009, 30(36): 6867–6878
[39] Mori M, Yamaguchi M, Sumitomo S,
. Hyaluronan-based biomaterials in tissue engineering.
Acta Histochemica et Cytochemica , 2004, 37(1): 1–5
[40] ?zgenel G Y. Effects of hyaluronic acid on peripheral nerve scarring and regeneration in rats.
Microsurgery , 2003, 23(6): 575–581
[41] Estes J M, Scott Adzick N, Harrison M R,
. Hyaluronate metabolism undergoes an ontogenic transition during fetal development: implications for scar-free wound healing.
Journal of Pediatric Surgery , 1993, 28(10): 1227–1231
[42] Campo G M, Avenoso A, Campo S,
. Molecular size hyaluronan differently modulates toll-like receptor-4 in LPS-induced inflammation in mouse chondrocytes.
Biochimie , 2010, 92(2): 204–215
[43] Khaing Z Z, Milman B D, Vanscoy J E,
. High molecular weight hyaluronic acid limits astrocyte activation and scar formation after spinal cord injury.
Journal of Neural Engineering , 2011, 8(4): 046033
[44] Wei Y T, Tian W M, Yu X,
. Hyaluronic acid hydrogels with IKVAV peptides for tissue repair and axonal regeneration in an injured rat brain.
Biomedical Materials , 2007, 2(3): S142–S146
[45] Ma J, Tian W M, Hou S P,
. An experimental test of stroke recovery by implanting a hyaluronic acid hydrogel carrying a Nogo receptor antibody in a rat model.
Biomedical Materials , 2007, 2(4): 233–240
[46] Lee K Y, Ha W S, Park W H. Blood compatibility and biodegradability of partially N-acylated chitosan derivatives.
Biomaterials , 1995, 16(16): 1211–1216
[47] Kim I Y, Seo S J, Moon H S,
. Chitosan and its derivatives for tissue engineering applications.
Biotechnology Advances , 2008, 26(1): 1–21
[48] Yuan Y, Zhang P Y, Yang Y M,
. The interaction of Schwann cells with chitosan membranes and fibers
in vitro.
Biomaterials , 2004, 25(18): 4273–4278
[49] Scanga V I, Goraltchouk A, Nussaiba N,
. Biomaterials for neural-tissue engineering - Chitosan supports the survival, migration, and differentiation of adult-derived neural stem and progenitor cells.
Canadian Journal of Chemistry , 2010, 88(3): 277–287
[50] Itoh S, Yamaguchi I, Suzuki M,
. Hydroxyapatite-coated tendon chitosan tubes with adsorbed laminin peptides facilitate nerve regeneration
in vivo.
Brain Research , 2003, 993(1-2): 111–123
[51] Rosales-Cortes M, Peregrina-Sandoval J, Ba?uelos-Pineda J,
. Regeneration of the axotomised sciatic nerve in dogs using the tubulisation technique with Chitosan biomaterial preloaded with progesterone.
Revista de Neurologia , 2003, 36(12): 1137–1141
[52] Chenite A, Buschmann M, Wang D,
. Rheological characterisation of thermogelling chitosan/glycerol-phosphate solutions.
Carbohydrate Polymers , 2001, 46(1): 39–47
[53] Crompton K E, Prankerd R J, Paganin D M,
. Morphology and gelation of thermosensitive chitosan hydrogels.
Biophysical Chemistry , 2005, 117(1): 47–53
[54] Chenite A, Chaput C, Wang D,
. Novel injectable neutral solutions of chitosan form biodegradable gels
in situ.
Biomaterials , 2000, 21(21): 2155–2161
[55] Crompton K E, Tomas D, Finkelstein D I,
. Inflammatory response on injection of chitosan/GP to the brain.
Journal of Materials Science: Materials in Medicine , 2006, 17(7): 633–639
[56] Barralet J E, Wang L, Lawson M,
. Comparison of bone marrow cell growth on 2D and 3D alginate hydrogels.
Journal of Materials Science: Materials in Medicine , 2005, 16(6): 515–519
[57] Dvir-Ginzberg M, Gamlieli-Bonshtein I, Agbaria R,
. Liver tissue engineering within alginate scaffolds: effects of cell-seeding density on hepatocyte viability, morphology, and function.
Tissue Engineering , 2003, 9(4): 757–766
[58] Mosahebi A, Simon M, Wiberg M,
. A novel use of alginate hydrogel as Schwann cell matrix.
Tissue Engineering , 2001, 7(5): 525–534
[59] Frampton J P, Hynd M R, Shuler M L,
. Fabrication and optimization of alginate hydrogel constructs for use in 3D neural cell culture.
Biomedical Materials , 2011, 6(1): 015002
[60] Ashton R S, Banerjee A, Punyani S,
. Scaffolds based on degradable alginate hydrogels and poly(lactide-
co-glycolide) microspheres for stem cell culture.
Biomaterials , 2007, 28(36): 5518–5525
[61] Suzuki Y, Kitaura M, Wu S F,
. Electrophysiological and horseradish peroxidase-tracing studies of nerve regeneration through alginate-filled gap in adult rat spinal cord.
Neuroscience Letters , 2002, 318(3): 121–124
[62] Kobayashi K, Huang C I, Lodge T P. Thermoreversible gelation of aqueous methylcellulose solutions.
Macromolecules , 1999, 32(21): 7070–7077
[63] Tate M C, Shear D A, Hoffman S W,
. Biocompatibility of methylcellulose-based constructs designed for intracerebral gelation following experimental traumatic brain injury.
Biomaterials , 2001, 22(10): 1113–1123
[64] Gros T, Sakamoto J S, Blesch A,
. Regeneration of long-tract axons through sites of spinal cord injury using templated agarose scaffolds.
Biomaterials , 2010, 31(26): 6719–6729
[65] Hejcl A, Lesny P, Prádny M,
. Biocompatible hydrogels in spinal cord injury repair.
Physiological Research , 2008, 57(Suppl 3): S121–S132
[66] Giannetti S, Lauretti L, Fernandez E,
. Acrylic hydrogel implants after spinal cord lesion in the adult rat.
Neurological Research , 2001, 23(4): 405–409
[67] Flynn L, Dalton P D, Shoichet M S. Fiber templating of poly(2-hydroxyethyl methacrylate) for neural tissue engineering.
Biomaterials , 2003, 24(23): 4265–4272
[68] Tsai E C, Dalton P D, Shoichet M S,
. Synthetic hydrogel guidance channels facilitate regeneration of adult rat brainstem motor axons after complete spinal cord transection.
Journal of Neurotrauma , 2004, 21(6): 789–804
[69] Yu T T, Shoichet M S. Guided cell adhesion and outgrowth in peptide-modified channels for neural tissue engineering.
Biomaterials , 2005, 26(13): 1507–1514
[70] Lesny P, Prádny M, Jendelová P,
. Macroporous hydrogels based on 2-hydroxyethyl methacrylate. Part 4: growth of rat bone marrow stromal cells in three-dimensional hydrogels with positive and negative surface charges and in polyelectrolyte complexes.
Journal of Materials Science: Materials in Medicine , 2006, 17(9): 829–833
[71] Hejcl A, Lesny P, Pradny M,
. Macroporous hydrogels based on 2-hydroxyethyl methacrylate. Part 6: 3D hydrogels with positive and negative surface charges and polyelectrolyte complexes in spinal cord injury repair.
Journal of Materials Science: Materials in Medicine , 2009, 20(7): 1571–1577
[72] Tsai E C, Dalton P D, Shoichet M S,
. Matrix inclusion within synthetic hydrogel guidance channels improves specific supraspinal and local axonal regeneration after complete spinal cord transection.
Biomaterials , 2006, 27(3): 519–533
[73] Kapur T A, Shoichet M S. Immobilized concentration gradients of nerve growth factor guide neurite outgrowth.
Journal of Biomedical Materials Research Part A , 2004, 68A(2): 235–243
[74] Woerly S, Pinet E, De Robertis L,
. Heterogeneous PHPMA hydrogels for tissue repair and axonal regeneration in the injured spinal cord.
Journal of Biomaterials Science, Polymer Edition , 1998, 9(7): 681–711
[75] Woerly S, Doan V D, Sosa N,
. Prevention of gliotic scar formation by NeuroGel
TM allows partial endogenous repair of transected cat spinal cord.
Journal of Neuroscience Research , 2004, 75(2): 262–272
[76] Hejcl A, Sedy J, Kapcalova M,
. HPMA-RGD hydrogels seeded with mesenchymal stem cells improve functional outcome in chronic spinal cord injury.
Stem Cells and Development , 2010, 19(10): 1535–1546
[77] Xu X M, Chen A, Guénard V,
. Bridging Schwann cell transplants promote axonal regeneration from both the rostral and caudal stumps of transected adult rat spinal cord.
Journal of Neurocytology , 1997, 26(1): 1–16
[78] Borgens R B, Shi R Y, Bohnert D. Behavioral recovery from spinal cord injury following delayed application of polyethylene glycol.
The Journal of Experimental Biology , 2002, 205(1): 1–12
[79] Burdick J A, Ward M, Liang E,
. Stimulation of neurite outgrowth by neurotrophins delivered from degradable hydrogels.
Biomaterials , 2006, 27(3): 452–459
[80] Piantino J, Burdick J A, Goldberg D,
. An injectable, biodegradable hydrogel for trophic factor delivery enhances axonal rewiring and improves performance after spinal cord injury.
Experimental Neurology , 2006, 201(2): 359–367
[81] Lampe K J, Mooney R G, Bjugstad K B,
. Effect of macromer weight percent on neural cell growth in 2D and 3D nondegradable PEG hydrogel culture.
Journal of Biomedical Materials Research Part A , 2010, 94(4): 1162–1171
[82] Xie J W, MacEwan M R, Schwartz A G,
. Electrospun nanofibers for neural tissue engineering.
Nanoscale , 2010, 2(1): 35–44
[83] Smith L A, Ma P X. Nano-fibrous scaffolds for tissue engineering.
Colloids and Surfaces B: Biointerfaces , 2004, 39(3): 125–131
[84] Wang W, Itoh S, Matsuda A,
. Influences of mechanical properties and permeability on chitosan nano/microfiber mesh tubes as a scaffold for nerve regeneration.
Journal of Biomedical Materials Research Part A , 2008, 84A(2): 557–566
[85] Liu T, Teng W K, Chan B P,
. Photochemical crosslinked electrospun collagen nanofibers: synthesis, characterization and neural stem cell interactions.
Journal of Biomedical Materials Research Part A , 2010, 95A(1): 276–282
[86] Wang W, Itoh S, Konno K,
. Effects of Schwann cell alignment along the oriented electrospun chitosan nanofibers on nerve regeneration.
Journal of Biomedical Materials Research Part A , 2009, 91A(4): 994–1005
[87] Hurtado A, Cregg J M, Wang H B,
. Robust CNS regeneration after complete spinal cord transection using aligned poly-L-lactic acid microfibers.
Biomaterials , 2011, 32(26): 6068–6079
[88] Yang F, Murugan R, Wang S,
. Electrospinning of nano/micro scale poly(L-lactic acid) aligned fibers and their potential in neural tissue engineering.
Biomaterials , 2005, 26(15): 2603–2610
[89] Gertz C C, Leach M K, Birrell L K,
. Accelerated neuritogenesis and maturation of primary spinal motor neurons in response to nanofibers.
Developmental Neurobiology , 2010, 70(8): 589–603
[90] Corey J M, Gertz C C, Wang B S,
. The design of electrospun PLLA nanofiber scaffolds compatible with serum-free growth of primary motor and sensory neurons.
Acta Biomaterialia , 2008, 4(4): 863–875
[91] Bechara S L, Judson A, Popat K C. Template synthesized poly(?-caprolactone) nanowire surfaces for neural tissue engineering.
Biomaterials , 2010, 31(13): 3492–3501
[92] Subramanian A, Krishnan U M, Sethuraman S. Fabrication of uniaxially aligned 3D electrospun scaffolds for neural regeneration.
Biomedical Materials , 2011, 6(2): 025004
[93] Christopherson G T, Song H, Mao H Q. The influence of fiber diameter of electrospun substrates on neural stem cell differentiation and proliferation.
Biomaterials , 2009, 30(4): 556–564
[94] Carlberg B, Axell M Z, Nannmark U,
. Electrospun polyurethane scaffolds for proliferation and neuronal differentiation of human embryonic stem cells.
Biomedical Materials , 2009, 4(4): 045004
[95] Corey J M, Lin D Y, Mycek K B,
. Aligned electrospun nanofibers specify the direction of dorsal root ganglia neurite growth.
Journal of Biomedical Materials Research Part A , 2007, 83A(3): 636–645
[96] Xie J, Willerth S M, Li X,
. The differentiation of embryonic stem cells seeded on electrospun nanofibers into neural lineages.
Biomaterials , 2009, 30(3): 354–362
[97] Zhao X, Pan F, Xu H,
. Molecular self-assembly and applications of designer peptide amphiphiles.
Chemical Society Reviews , 2010, 39(9): 3480–3498
[98] Semino C E, Kasahara J, Hayashi Y,
. Entrapment of migrating hippocampal neural cells in three-dimensional peptide nanofiber scaffold.
Tissue Engineering , 2004, 10(3-4): 643–655
[99] Holmes T C, de Lacalle S, Su X,
. Extensive neurite outgrowth and active synapse formation on self-assembling peptide scaffolds.
Proceedings of the National Academy of Sciences of the United States of America , 2000, 97(12): 6728–6733
[100] Silva G A, Czeisler C, Niece K L,
. Selective differentiation of neural progenitor cells by high-epitope density nanofibers.
Science , 2004, 303(5662): 1352–1355
[101] Tysseling-Mattiace V M, Sahni V, Niece K L,
. Self-assembling nanofibers inhibit glial scar formation and promote axon elongation after spinal cord injury.
The Journal of Neuroscience , 2008, 28(14): 3814–3823
[102] Ellis-Behnke R G, Liang Y X, You S W,
. Nano neuro knitting: peptide nanofiber scaffold for brain repair and axon regeneration with functional return of vision.
Proceedings of the National Academy of Sciences of the United States of America , 2006, 103(13): 5054–5059
[103] Geiger B, Spatz J P, Bershadsky A D. Environmental sensing through focal adhesions.
Nature Reviews Molecular Cell Biology , 2009, 10(1): 21–33
[104] Curran J M, Chen R, Hunt J A. Controlling the phenotype and function of mesenchymal stem cells
in vitro by adhesion to silane-modified clean glass surfaces.
Biomaterials , 2005, 26(34): 7057–7067
[105] Ulman A. Formation and structure of self-assembled monolayers.
Chemical Reviews , 1996, 96(4): 1533–1554
[106] Phillips J E, Petrie T A, Creighton F P,
. Human mesenchymal stem cell differentiation on self-assembled monolayers presenting different surface chemistries.
Acta Biomaterialia , 2010, 6(1): 12–20
[107] Faucheux N, Schweiss R, Lützow K,
. Self-assembled monolayers with different terminating groups as model substrates for cell adhesion studies.
Biomaterials , 2004, 25(14): 2721–2730
[108] Barbosa J N, Barbosa M A, Aguas A P. Adhesion of human leukocytes to biomaterials: an
in vitro study using alkanethiolate monolayers with different chemically functionalized surfaces.
Journal of Biomedical Materials Research Part A , 2003, 65(4): 429–434
[109] Inoue S, Imamura M, Umezawa A,
. Attachment, proliferation and adipogenic differentiation of adipo-stromal cells on self-assembled monolayers of different chemical compositions.
Journal of Biomaterials Science, Polymer Edition , 2008, 19(7): 893–914
[110] Keselowsky B G, Collard D M, García A J. Integrin binding specificity regulates biomaterial surface chemistry effects on cell differentiation.
Proceedings of the National Academy of Sciences of the United States of America , 2005, 102(17): 5953–5957
[111] Keselowsky B G, Collard D M, García A J. Surface chemistry modulates focal adhesion composition and signaling through changes in integrin binding.
Biomaterials , 2004, 25(28): 5947–5954
[112] Ren Y J, Zhang H, Huang H,
.
In vitro behavior of neural stem cells in response to different chemical functional groups.
Biomaterials , 2009, 30(6): 1036–1044
[113] Georges P C, Miller W J, Meaney D F,
. Matrices with compliance comparable to that of brain tissue select neuronal over glial growth in mixed cortical cultures.
Biophysical Journal , 2006, 90(8): 3012–3018
[114] Saha K, Keung A J, Irwin E F,
. Substrate modulus directs neural stem cell behavior.
Biophysical Journal , 2008, 95(9): 4426–4438
[115] Lynam D, Bednark B, Peterson C,
. Precision microchannel scaffolds for central and peripheral nervous system repair.
Journal of Materials Science: Materials in Medicine , 2011, 22(9): 2119–2130
[116] Wong D Y, Leveque J C, Brumblay H,
. Macro-architectures in spinal cord scaffold implants influence regeneration.
Journal of Neurotrauma , 2008, 25(8): 1027–1037
[117] Scott J B, Afshari M, Kotek R,
. The promotion of axon extension
in vitro using polymer-templated fibrin scaffolds.
Biomaterials , 2011, 32(21): 4830–4839
[118] Stokols S, Sakamoto J, Breckon C,
. Templated agarose scaffolds support linear axonal regeneration.
Tissue Engineering , 2006, 12(10): 2777–2787
[119] Stokols S, Tuszynski M H. Freeze-dried agarose scaffolds with uniaxial channels stimulate and guide linear axonal growth following spinal cord injury.
Biomaterials , 2006, 27(3): 443–451
[120] M?llers S, Heschel I, Damink L H H O,
. Cytocompatibility of a novel, longitudinally microstructured collagen scaffold intended for nerve tissue repair.
Tissue Engineering Part A , 2009, 15(3): 461–472
[121] Luo Y, Shoichet M S. A photolabile hydrogel for guided three-dimensional cell growth and migration.
Nature Materials , 2004, 3(4): 249–253
[122] Xie J W, MacEwan M R, Li X R,
. Neurite outgrowth on nanofiber scaffolds with different orders, structures, and surface properties.
ACS Nano , 2009, 3(5): 1151–1159
[123] Cooper A, Bhattarai N, Zhang M. Fabrication and cellular compatibility of aligned chitosan-PCL fibers for nerve tissue regeneration.
Carbohydrate Polymers , 2011, 85(1): 149–156
[124] Cho Y I, Choi J S, Jeong S Y,
. Nerve growth factor (NGF)-conjugated electrospun nanostructures with topographical cues for neuronal differentiation of mesenchymal stem cells.
Acta Biomaterialia , 2010, 6(12): 4725–4733
[125] Xie J, Willerth S M, Li X,
. The differentiation of embryonic stem cells seeded on electrospun nanofibers into neural lineages.
Biomaterials , 2009, 30(3): 354–362
[126] Wang Y S, Yao M, Zhou J H,
. The promotion of neural progenitor cells proliferation by aligned and randomly oriented collagen nanofibers through β1 integrin/MAPK signaling pathway.
Biomaterials , 2011, 32(28): 6737–6744
[127] Liu B P, Fournier A, GrandPré T,
. Myelin-associated glycoprotein as a functional ligand for the Nogo-66 receptor.
Science , 2002, 297(5584): 1190–1193
[128] Domeniconi M, Cao Z U, Spencer T,
. Myelin-associated glycoprotein interacts with the Nogo66 receptor to inhibit neurite outgrowth.
Neuron , 2002, 35(2): 283–290
[129] Tian W M, Zhang C L, Hou S P,
. Hyaluronic acid hydrogel as Nogo-66 receptor antibody delivery system for the repairing of injured rat brain:
in vitro.
Journal of Controlled Release , 2005, 102(1): 13–22
[130] Hou S, Tian W, Xu Q,
. The enhancement of cell adherence and inducement of neurite outgrowth of dorsal root ganglia co-cultured with hyaluronic acid hydrogels modified with Nogo-66 receptor antagonist
in vitro.
Neuroscience , 2006, 137(2): 519–529
[131] Wei Y T, He Y, Xu C L,
. Hyaluronic acid hydrogel modified with nogo-66 receptor antibody and poly-L-lysine to promote axon regrowth after spinal cord injury.
Journal of Biomedical Materials Research Part B: Applied Biomaterials , 2010, 95B(1): 110–117
[132] Grendt S J, Rodriguez J L, Pawlik J W,
. Consequences of high-dose steroid therapy for acute spinal cord injury.
The Journal of Trauma Injury, Infection, and Critical Care , 1997, 42(2): 279–284
[133] Qian T, Guo X, Levi A D,
. High-dose methylprednisolone may cause myopathy in acute spinal cord injury patients.
Spinal Cord , 2005, 43(4): 199–203
[134] Chvatal S A, Kim Y-T, Bratt-Leal A M,
. Spatial distribution and acute anti-inflammatory effects of Methylprednisolone after sustained local delivery to the contused spinal cord.
Biomaterials , 2008, 29(12): 1967–1975
[135] Schaub N J, Gilbert R J. Controlled release of 6-aminonicotinamide from aligned, electrospun fibers alters astrocyte metabolism and dorsal root ganglia neurite outgrowth.
Journal of Neural Engineering , 2011, 8(4): 046026
[136] Sayer F T, Oudega M, Hagg T. Neurotrophins reduce degeneration of injured ascending sensory and corticospinal motor axons in adult rat spinal cord.
Experimental Neurology , 2002, 175(1): 282–296
[137] Novikova L N, Novikov L N, Kellerth J O. Survival effects of BDNF and NT-3 on axotomized rubrospinal neurons depend on the temporal pattern of neurotrophin administration.
European Journal of Neuroscience , 2000, 12(2): 776–780
[138] Giger R J, Hollis II E R, Tuszynski M H. Guidance molecules in axon regeneration.
Cold Spring Harbor Perspectives in Biology , 2010, 2(7): a001867
[139] Krewson C E, Klarman M L, Saltzman W M. Distribution of nerve growth factor following direct delivery to brain interstitium.
Brain Research , 1995, 680(1-2): 196–206
[140] Li X, Yang Z, Zhang A. The effect of neurotrophin-3/chitosan carriers on the proliferation and differentiation of neural stem cells.
Biomaterials , 2009, 30(28): 4978–4985
[141] Yu L M Y, Wosnick J H, Shoichet M S. Miniaturized system of neurotrophin patterning for guided regeneration.
Journal of Neuroscience Methods , 2008, 171(2): 253–263
[142] Dodla M C, Bellamkonda R V. Differences between the effect of anisotropic and isotropic laminin and nerve growth factor presenting scaffolds on nerve regeneration across long peripheral nerve gaps.
Biomaterials , 2008, 29(1): 33–46
[143] Jain A, Kim Y T, McKeon R J,
.
In situ gelling hydrogels for conformal repair of spinal cord defects, and local delivery of BDNF after spinal cord injury.
Biomaterials , 2006, 27(3): 497–504
[144] Park J, Lim E, Back S,
. Nerve regeneration following spinal cord injury using matrix metalloproteinase-sensitive, hyaluronic acid-based biomimetic hydrogel scaffold containing brain-derived neurotrophic factor.
Journal of Biomedical Materials Research Part A , 2010, 93(3): 1091–1099
[145] Iannotti C, Li H Y, Yan P,
. Glial cell line-derived neurotrophic factor-enriched bridging transplants promote propriospinal axonal regeneration and enhance myelination after spinal cord injury.
Experimental Neurology , 2003, 183(2): 379–393
[146] Wang Y C, Wu Y T, Huang H Y,
. Sustained intraspinal delivery of neurotrophic factor encapsulated in biodegradable nanoparticles following contusive spinal cord injury.
Biomaterials , 2008, 29(34): 4546–4553
[147] Bhang S H, Lee T J, Lim J M,
. The effect of the controlled release of nerve growth factor from collagen gel on the efficiency of neural cell culture.
Biomaterials , 2009, 30(1): 126–132
[148] Cooke M J, Wang Y F, Morshead C M,
. Controlled epi-cortical delivery of epidermal growth factor for the stimulation of endogenous neural stem cell proliferation in stroke-injured brain.
Biomaterials , 2011, 32(24): 5688–5697
[149] Mo L H, Yang Z Y, Zhang A F,
. The repair of the injured adult rat hippocampus with NT-3-chitosan carriers.
Biomaterials , 2010, 31(8): 2184–2192
[150] Taylor S J, Sakiyama-Elbert S E. Effect of controlled delivery of neurotrophin-3 from fibrin on spinal cord injury in a long term model.
Journal of Controlled Release , 2006, 116(2): 204–210
[151] Taylor S J, Rosenzweig E S, McDonald III J W,
. Delivery of neurotrophin-3 from fibrin enhances neuronal fiber sprouting after spinal cord injury.
Journal of Controlled Release , 2006, 113(3): 226–235
[152] Sakiyama-Elbert S E, Hubbell J A. Development of fibrin derivatives for controlled release of heparin-binding growth factors.
Journal of Controlled Release , 2000, 65(3): 389–402
[153] Willerth S M, Johnson P J, Maxwell D J,
. Rationally designed peptides for controlled release of nerve growth factor from fibrin matrices.
Journal of Biomedical Materials Research Part A , 2007, 80A(1): 13–23
[154] Johnson P J, Tatara A, Shiu A,
. Controlled release of neurotrophin-3 and platelet-derived growth factor from fibrin scaffolds containing neural progenitor cells enhances survival and differentiation into neurons in a subacute model of SCI.
Cell Transplantation , 2010, 19(1): 89–101
[155] Taylor S J, McDonald III J W, Sakiyama-Elbert S E. Controlled release of neurotrophin-3 from fibrin gels for spinal cord injury.
Journal of Controlled Release , 2004, 98(2): 281–294
[156] Rahman N, Purpura K A, Wylie R G,
. The use of vascular endothelial growth factor functionalized agarose to guide pluripotent stem cell aggregates toward blood progenitor cells.
Biomaterials , 2010, 31(32): 8262–8270
[157] Shen Y H, Shoichet M S, Radisic M. Vascular endothelial growth factor immobilized in collagen scaffold promotes penetration and proliferation of endothelial cells.
Acta Biomaterialia , 2008, 4(3): 477–489
[158] Cho Y I, Choi J S, Jeong S Y,
. Nerve growth factor (NGF)-conjugated electrospun nanostructures with topographical cues for neuronal differentiation of mesenchymal stem cells.
Acta Biomaterialia , 2010, 6(12): 4725–4733
[159] Xu X Y, Geremia N, Bao F,
. Schwann cell coculture improves the therapeutic effect of bone marrow stromal cells on recovery in spinal cord-injured mice.
Cell Transplantation , 2011, 20(7): 1065–1086
[160] Schnell E, Klinkhammer K, Balzer S,
. Guidance of glial cell migration and axonal growth on electrospun nanofibers of poly-
?-caprolactone and a collagen/poly-
?-caprolactone blend.
Biomaterials , 2007, 28(19): 3012–3025
[161] Guo J, Su H, Zeng Y,
. Reknitting the injured spinal cord by self-assembling peptide nanofiber scaffold.
Nanomedicine: Nanotechnology, Biology and Medicine , 2007, 3(4): 311–321
[162] Shen Y X, Qian Y Q, Zhang H X,
. Guidance of olfactory ensheathing cell growth and migration on electrospun silk fibroin scaffolds.
Cell Transplantation , 2010, 19(2): 147–157
[163] Lu D, Mahmood A, Qu C,
. Collagen scaffolds populated with human marrow stromal cells reduce lesion volume and improve functional outcome after traumatic brain injury.
Neurosurgery , 2007, 61(3): 596–603
[164] Xiong Y, Qu C S, Mahmood A,
. Delayed transplantation of human marrow stromal cell-seeded scaffolds increases transcallosal neural fiber length, angiogenesis, and hippocampal neuronal survival and improves functional outcome after traumatic brain injury in rats.
Brain Research , 2009, 1263: 183–191
[165] Ren Y J, Zhou Z Y, Liu B F,
. Preparation and characterization of fibroin/hyaluronic acid composite scaffold.
International Journal of Biological Macromolecules , 2009, 44(4): 372–378
[166] Yu H W, Cao B, Feng M Y,
. Combinated transplantation of neural stem cells and collagen type I promote functional recovery after cerebral ischemia in rats.
The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology , 2010, 293(5): 911–917
[167] Oudega M, Xu X M. Schwann cell transplantation for repair of the adult spinal cord.
Journal of Neurotrauma , 2006, 23(3-4): 453–467
[168] Mirsky R, Jessen K R, Brennan A,
. Schwann cells as regulators of nerve development.
Journal of Physiology- Paris , 2002, 96(1-2): 17–24
[169] Boruch A V, Conners J J, Pipitone M,
. Neurotrophic and migratory properties of an olfactory ensheathing cell line.
Glia , 2001, 33(3): 225–229
[170] Au E, Roskams A J. Olfactory ensheathing cells of the lamina propria
in vivo and
in vitro.
Glia , 2003, 41(3): 224–236
[171] Ramer L M, Au E, Richter M W,
. Peripheral olfactory ensheathing cells reduce scar and cavity formation and promote regeneration after spinal cord injury.
The Journal of Comparative Neurology , 2004, 473(1): 1–15
[172] Li B C, Jiao S S, Xu C A,
. PLGA conduit seeded with olfactory ensheathing cells for bridging sciatic nerve defect of rats.
Journal of Biomedical Materials Research Part A , 2010, 94(3): 769–780
[173] Cao Q L, Zhang Y P, Howard R M,
. Pluripotent stem cells engrafted into the normal or lesioned adult rat spinal cord are restricted to a glial lineage.
Experimental Neurology , 2001, 167(1): 48–58
[174] Zurita M, Vaquero J. Functional recovery in chronic paraplegia after bone marrow stromal cells transplantation.
Neuroreport , 2004, 15(7): 1105–1108
[175] Mahmood A, Lu D, Wang L,
. Treatment of traumatic brain injury in female rats with intravenous administration of bone marrow stromal cells.
Neurosurgery , 2001, 49(5): 1196–1204
[176] Gerardo-Nava J, Führmann T, Klinkhammer K,
. Human neural cell interactions with orientated electrospun nanofibers
in vitro.
Nanomedicine: Nanotechnology, Biology and Medicine , 2009, 4(1): 11–30
[177] Prabhakaran M P, Venugopal J R, Ramakrishna S. Mesenchymal stem cell differentiation to neuronal cells on electrospun nanofibrous substrates for nerve tissue engineering.
Biomaterials , 2009, 30(28): 4996–5003
[178] Fukushima K, Enomoto M, Tomizawa S,
. The axonal regeneration across a honeycomb collagen sponge applied to the transected spinal cord.
Journal of Medical and Dental Sciences , 2008, 55(1): 71–79
[179] Koh H S, Yong T, Chan C K,
. Enhancement of neurite outgrowth using nano-structured scaffolds coupled with laminin.
Biomaterials , 2008, 29(26): 3574–3582
[180] Mukhatyar V J, Salmerón-Sánchez M, Rudra S,
. Role of fibronectin in topographical guidance of neurite extension on electrospun fibers.
Biomaterials , 2011, 32(16): 3958–3968
[181] Li W, Guo Y, Wang H,
. Electrospun nanofibers immobilized with collagen for neural stem cells culture.
Journal of Materials Science: Materials in Medicine , 2008, 19(2): 847–854
[182] Hashemi S M, Soudi S, Shabani I,
. The promotion of stemness and pluripotency following feeder-free culture of embryonic stem cells on collagen-grafted 3-dimensional nanofibrous scaffold.
Biomaterials , 2011, 32(30): 7363–7374
[183] Borkenhagen M, Clémence J-F, Sigrist H,
. Three-dimensional extracellular matrix engineering in the nervous system.
Journal of Biomedical Materials Research , 1998, 40(3): 392–400
[184] Cui F Z, Tian W M, Hou S P,
. Hyaluronic acid hydrogel immobilized with RGD peptides for brain tissue engineering.
Journal of Materials Science: Materials in Medicine , 2006, 17(12): 1393–1401
[185] Suzuki M, Itoh S, Yamaguchi I,
. Tendon chitosan tubes covalently coupled with synthesized laminin peptides facilitate nerve regeneration
in vivo.
Journal of Neuroscience Research , 2003, 72(5): 646–659
[186] Schense J C, Bloch J, Aebischer P,
. Enzymatic incorporation of bioactive peptides into fibrin matrices enhances neurite extension.
Nature Biotechnology , 2000, 18(4): 415–419
[187] Spitzer N C. Electrical activity in early neuronal development.
Nature , 2006, 444(7120): 707–712
[188] Ramakers G J A, Winter J, Hoogland T M,
. Depolarization stimulates lamellipodia formation and axonal but not dendritic branching in cultured rat cerebral cortex neurons.
Developmental Brain Research , 1998, 108(1-2): 205–216
[189] Kerns J M, Fakhouri A J, Weinrib H P,
. Electrical stimulation of nerve regeneration in the rat: the early effects evaluated by a vibrating probe and electron microscopy.
Neuroscience , 1991, 40(1): 93–107
[190] Borgens R B, Bohnert D M. The responses of mammalian spinal axons to an applied DC voltage gradient.
Experimental Neurology , 1997, 145(2): 376–389
[191] Kotwal A, Schmidt C E. Electrical stimulation alters protein adsorption and nerve cell interactions with electrically conducting biomaterials.
Biomaterials , 2001, 22(10): 1055–1064
[192] Schmidt C E, Shastri V R, Vacanti J P,
. Stimulation of neurite outgrowth using an electrically conducting polymer.
Proceedings of the National Academy of Sciences of the United States of America , 1997, 94(17): 8948–8953
[193] Kim D H, Richardson-Burns S M, Hendricks J L,
. Effect of immobilized nerve growth factor on conductive polymers: Electrical properties and cellular response.
Advanced Functional Materials , 2007, 17(1): 79–86
[194] Stauffer W R, Cui X T. Polypyrrole doped with 2 peptide sequences from laminin.
Biomaterials , 2006, 27(11): 2405–2413
[195] Xie J, Macewan M R, Willerth S M,
. Conductive core-sheath nanofibers and their potential application in neural tissue engineering.
Advanced Functional Materials , 2009, 19(14): 2312–2318
[196] Lee J Y, Bashur C A, Goldstein A S,
. Polypyrrole-coated electrospun PLGA nanofibers for neural tissue applications.
Biomaterials , 2009, 30(26): 4325–4335
[197] Collier J H, Camp J P, Hudson T W,
. Synthesis and characterization of polypyrrole-hyaluronic acid composite biomaterials for tissue engineering applications.
Journal of Biomedical Materials Research , 2000, 50(4): 574–584
[198] Runge M B, Dadsetan M, Baltrusaitis J,
. The development of electrically conductive polycaprolactone fumarate-polypyrrole composite materials for nerve regeneration.
Biomaterials , 2010, 31(23): 5916–5926
[199] Rivers T J, Hudson T W, Schmidt C E. Synthesis of a novel, biodegradable electrically conducting polymer for biomedical applications.
Advanced Functional Materials , 2002, 12(1): 33–37
[200] Tran P A, Zhang L, Webster T J. Carbon nanofibers and carbon nanotubes in regenerative medicine.
Advanced Drug Delivery Reviews , 2009, 61(12): 1097–1114
[201] Li X M, Gao H, Uo M,
. Effect of carbon nanotubes on cellular functions
in vitro.
Journal of Biomedical Materials Research Part A , 2009, 91A(1): 132–139
[202] Cellot G, Cilia E, Cipollone S,
. Carbon nanotubes might improve neuronal performance by favouring electrical shortcuts.
Nature Nanotechnology , 2009, 4(2): 126–133
[203] Jin G Z, Kim M, Shin U S,
. Neurite outgrowth of dorsal root ganglia neurons is enhanced on aligned nanofibrous biopolymer scaffold with carbon nanotube coating.
Neuroscience Letters , 2011, 501(1): 10–14
[204] Abdullah C A C, Asanithi P, Brunner E W,
. Aligned, isotropic and patterned carbon nanotube substrates that control the growth and alignment of Chinese hamster ovary cells.
Nanotechnology , 2011, 22(20): 205102
[205] Lewitus D Y, Landers J, Branch J R,
. Biohybrid carbon nanotube/agarose fibers for neural tissue engineering.
Advanced Functional Materials , 2011, 21(14): 2624–2632
[206] Lee H J, Park J, Yoon O J,
. Amine-modified single-walled carbon nanotubes protect neurons from injury in a rat stroke model.
Nature Nanotechnology , 2011, 6(2): 121–125
[207] Allen B L, Kichambare P D, Gou P,
. Biodegradation of single-walled carbon nanotubes through enzymatic catalysis.
Nano Letters , 2008, 8(11): 3899–3903
[208] Kagan V E, Konduru N V, Feng W H,
. Carbon nanotubes degraded by neutrophil myeloperoxidase induce less pulmonary inflammation.
Nature Nanotechnology , 2010, 5(5): 354–359
[209] Li X, Yang Z, Zhang A,
. Repair of thoracic spinal cord injury by chitosan tube implantation in adult rats.
Biomaterials , 2009, 30(6): 1121–1132