AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (1.2 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Review | Open Access

Nanofibrous scaffolds supporting optimal central nervous system regeneration: an evidence-based review

Munyaradzi KamudzanduPaul RoachRosemary A FrickerYing Yang( )
Institute for Science and Technology in Medicine, School of Medicine, Keele University, Stoke-on-Trent, UK
Show Author Information

Abstract

Restoration of function following damage to the central nervous system (CNS) is severely restricted by several factors. These include the hindrance of axonal regeneration imposed by glial scars resulting from inflammatory response to damage, and limited axonal outgrowth toward target tissue. Strategies for promoting CNS functional regeneration include the use of nanotechnology. Due to their structural similarity, synthetic nanofibers could play an important role in regeneration of CNS neural tissue toward restoration of function following injury. Two-dimensional nanofibrous scaffolds have been used to provide contact guidance for developing brain and spinal cord neurites, particularly from neurons cultured in vitro. Three-dimensional nanofibrous scaffolds have been used, both in vitro and in vivo, for creating cell adhesion permissive milieu, in addition to contact guidance or structural bridges for axons, to control reconnection in brain and spinal cord injury models. It is postulated that nanofibrous scaffolds made from biodegradable and biocompatible materials can become powerful structural bridges for both guiding the outgrowth of neurites and rebuilding glial circuitry over the "lesion gaps" resulting from injury in the CNS.

References

1.
Huang H, Chen L, Sanberg P. Cell therapy from bench to bedside translation in CNS neurorestoratology era. Cell Med. 2010;1(1):15–46.
2.
Huang H, Chen L. Neurorestorative process, law, and mechanisms. Journal of Neurorestoratology. 2015;3:23–30.
3.
Horner PJ, Gage FH. Regenerating the damaged central nervous system. Nature. 2000;407(6807):963–970.
4.
Taylor JSH, Bampton ETW. Factors secreted by Schwann cells stimulate the regeneration of neonatal retinal ganglion cells. J Anat. 2004;204(1):25–31.
5.
Stoll G, Griffin JW, Li CY, Trapp BD. Wallerian degeneration in the peripheral nervous system: participation of both Schwann cells and macrophages in myelin degradation. J Neurocytol. 1989;18(5):671–683.
6.
Schmidt CE, Leach JB. Neural tissue engineering: strategies for repair and regeneration. Annu Rev Biomed Eng. 2003;5:293–347.
7.
Tian L, Prabhakaran MP, Ramakrishna S. Strategies for regeneration of components of nervous system: scaffolds, cells and biomolecules. Regenerative Biomaterials. 2015;2(1):31–45.
8.
Kalil K, Reh T. A light and electron microscopic study of regrowing pyramidal tract fibers. J Comp Neurol. 1982;211(3):265–275.
9.
Pasterkamp RJ, Giger RJ, Ruitenberg MJ, et al. 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. Mol Cell Neurosci. 1999;13(2):143–166.
10.
Rhodes KE, Fawcett JW. Chondroitin sulphate proteoglycans: preventing plasticity or protecting the CNS? J Anat. 2004;204(1):33–48.
11.
McKeon RJ, Schreiber RC, Rudge JS, Silver J. Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhibitory molecules on reactive astrocytes. J Neurosci. 1991;11(11):3398–3411.
12.
Perry VH, Brown MC, Gordon S. The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration. J Exp Med. 1987;165(4):1218–1223.
13.
Stoll G, Trapp BD, Griffin JW. Macrophage function during Wallerian degeneration of rat optic nerve: clearance of degenerating myelin and Ia expression. J Neurosci. 1989;9(7):2327–2335.
14.
Obeso JA, Rodriguez-Oroz MC, Stamelou M, Bhatia KP, Burn DJ. The expanding universe of disorders of the basal ganglia. Lancet. 2014;384(9942):523–531.
15.
Utter AA, Basso MA. The basal ganglia: an overview of circuits and function. Neurosci Biobehav Rev. 2008;32(3):333–342.
16.
Han D, Cheung KC. Biodegradable cell-seeded nanofiber scaffolds for neural repair. Polymers. 2011;3(4):1684–1733.
17.
Houweling DA, Lankhorst AJ, Gispen WH, Bär PR, Joosten EA. Collagen containing neurotrophin-3 (NT-3) attracts regrowing injured corticospinal axons in the adult rat spinal cord and promotes partial functional recovery. Exp Neurol. 1998;153(1):49–59.
18.
Ramón-Cueto A, Plant GW, Avila J, Bunge MB. Long-distance axonal regeneration in the transected adult rat spinal cord is promoted by olfactory ensheathing glia transplants. J Neurosci. 1998;18(10):3803–3815.
19.
Guan J, Fujimoto KL, Sacks MS, Wagner WR. Preparation and characterization of highly porous, biodegradable polyurethane scaffolds for soft tissue applications. Biomaterials. 2005;26(18):3961–3971.
20.
Martínez-Pérez C, Olivas-Armendariz I, Castro-Carmona JS, García-Casillas PE. Scaffolds for tissue engineering via thermally induced phase separation. In: Wislet-Gendebien S, editor. Advances in Regenerative Medicine. InTech; 2011:275–294. Available from: http://orbi.ulg.ac.be/bitstream/2268/101891/1/Advances_in_Regenerative_Medicine.pdf#page=287. Accessed January 11, 2015.
21.
Zhong C, Cooper A, Kapetanovic A, Fang Z, Zhang M, Rolandi M. A facile bottom-up route to self-assembled biogenic chitin nanofibers. Soft Matter. 2010;6(21):5298–5301.
22.
Kim SW, Han SO, Sim IN, Cheon JY, Park WH. Fabrication and characterization of cellulose acetate/montmorillonite composite nanofibers by electrospinning. Journal of Nanomaterials. 2015;.
23.
Pham QP, Sharma U, Mikos AG. Electrospinning of polymeric nanofibers for tissue engineering applications: a review. Tissue Eng. 2006;12(5):1197–1211.
24.
Huang Z-M, Zhang Y-Z, Kotaki M, Ramakrishna S. A review on polymer nanofibers by electrospinning and their applications in nanocomposites. Composites Science and Technology. 2003;63(15):2223–2253.
25.
Bhardwaj N, Kundu SC. Electrospinning: a fascinating fiber fabrication technique. Biotechnol Adv. 2010;28(3):325–347.
26.
Garg K, Bowlin GL. Electrospinning jets and nanofibrous structures. Biomicrofluidics. 2011;5(1):1–19.
27.
Li D, Xia Y. Electrospinning of canofibers: reinventing the wheel? Advanced Materials. 2004;16(14):1151–1170.
28.
Sill TJ, von Recum HA. Electrospinning: applications in drug delivery and tissue engineering. Biomaterials. 2008;29(13):1989–2006.
29.
Lee Y-S, Livingston Arinzeh T. Electrospun nanofibrous materials for neural tissue engineering. Polymers. 2011;3(1):413–426.
30.
Liu H, Ding X, Zhou G, Li P, Wei X, Fan Y. Electrospinning of nanofibers for tissue engineering applications. Journal of Nanomaterials. 2013;2013:1–11.
31.
Yang F, Murugan R, Wang S, Ramakrishna 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.
32.
Li Z, Wang C. Effects of working parameters on electrospinning. In: One-Dimensional nanostructures: Electrospinning Technique and Unique Nanofibers. SpringerBriefs in Materials. Berlin, Heidelberg: Springer Berlin Heidelberg; 2013:15–29.
33.
Okutan N, Terzi P, Altay F. Affecting parameters on electrospinning process and characterization of electrospun gelatin nanofibers. Food Hydrocolloids. 2014;39:19–26.
34.
Corey JM, Gertz CC, Johnson SL, et al. The design of electrospun PLLA nanofiber scaffolds compatible with serum-free growth of primary motor and sensory neurons. Acta Biomater. 2008;4(4):863–875.
35.
Boland ED, Wnek GE, Simpson DG, Pawlowski KJ, Bowlin GL. Tailoring tissue engineering scaffolds using electrostatic processing techniques: A study of poly(glycolic acid) electrospinning. Journal of Macromolecular Science, Part A. 2001;38(12):1231–1243.
36.
Schnell E, Klinkhammer K, Balzer S, et al. Guidance of glial cell migration and axonal growth on electrospun nanofibers of poly-epsilon-caprolactone and a collagen/poly-epsilon-caprolactone blend. Biomaterials. 2007;28(19):3012–3025.
37.
Chen H, Fan X, Xia J, et al. Electrospun chitosan-graft-poly (ε-caprolactone)/poly (ε-caprolactone) nanofibrous scaffolds for retinal tissue engineering. Int J Nanomedicine. 2011;6:453–461.
38.
Boland ED, Telemeco TA, Simpson DG, Wnek GE, Bowlin GL. Utilizing acid pretreatment and electrospinning to improve biocompatibility of poly(glycolic acid) for tissue engineering. J Biomed Mater Res B Appl Biomater. 2004;71(1):144–152.
39.
Carnell LS, Siochi EJ, Holloway NM, et al. Aligned mats from electrospun single fibers. Macromolecules. 2008;41(14):5345–5349.
40.
Matthews JA, Wnek GE, Simpson DG, Bowlin GL. Electrospinning of collagen nanofibers. Biomacromolecules. 2002;3(2):232–238.
41.
Zhong S, Teo WE, Zhu X, Beuerman RW, Ramakrishna S, Yung LYL. An aligned nanofibrous collagen scaffold by electrospinning and its effects on in vitro fibroblast culture. J Biomed Mater Res A. 2006;79(3):456–463.
42.
Punnoose AM, Elamparithi A, Kuruvilla S. Electrospun type 1 collagen matrices using a novel benign solvent for cardiac tissue engineering. Journal of Cellular Physiology. 2015;(August 2014).
43.
Panzavolta S, Gioffrè M, Focarete ML, Gualandi C, Foroni L, Bigi A. Electrospun gelatin nanofibers: optimization of genipin cross-linking to preserve fiber morphology after exposure to water. Acta Biomaterialia. 2011;7(4):1702–1709.
44.
Maleknia L, Majdi ZR. Electrospinning of Gelatin Nanofiber for Biomedical Application. Orient J Chem. 2014;30(4).
45.
Haider S, Al-Zeghayer Y, Ahmed Ali FA, et al. Highly aligned narrow diameter chitosan electrospun nanofibers. J Polym Res. 2013;20(105), .
46.
Lee SJ, Heo DN, Moon JH, et al. Electrospun chitosan nanofibers with controlled levels of silver nanoparticles. Preparation, characterization and antibacterial activity. Carbohydrate Polymers. 2014;111:530–537.
47.
Wang J, Ye R, Wei Y, et al. The effects of electrospun TSF nanofiber diameter and alignment on neuronal differentiation of human embryonic stem cells. J Biomed Mater Res A. 2012;100(3):632–645.
48.
Liu Z, Zhang F, Ming J, Bie S, Li J, Zuo B. Preparation of electrospun silk fibroin nanofibers from solutions containing native silk fibrils. Journal of Applied Polymer Science. 2014;132(1).
49.
Kamudzandu M, Yang Y, Roach P, Fricker RA. Efficient alignment of primary CNS neurites using structurally engineered surfaces and biochemical cues. RSC Adv. 2015;5(28):22053–22059.
50.
Wen X, Tresco PA. Effect of filament diameter and extracellular matrix molecule precoating on neurite outgrowth and Schwann cell behavior on multifilament entubulation bridging device in vitro. Journal of Biomedical Materials Research. Part A. 2006;76A(3):626–637.
51.
Kalil K, Dent EW. Touch and go: guidance cues signal to the growth cone cytoskeleton. Current Opinion in Neurobiology. 2005;15(5):521–526.
52.
Kolodkin AL, Tessier-Lavigne M. Mechanisms and molecules of neuronal wiring: a primer. Cold Spring Harb Perspect Biol. 2011;3(6):pii: a001727.
53.
Gomez TM, Letourneau PC. Actin dynamics in growth cone motility and navigation. Journal of Neurochemistry. 2014;129(2):221–234.
54.
Purves D, Augustine GJ, Fitzpatrick D. Neuroscience. 2nd ed. Sunderland (MA): Sinauer Associates, Inc.; 2001.
55.
Curinga G, Smith GM. Molecular/genetic manipulation of extrinsic axon guidance factors for CNS repair and regeneration. Exp Neurol. 2008;209(2):333–342.
56.
Polleux F, Snider W. Initiating and growing an axon. Cold Spring Harb Perspect Biol. 2010;2(4):a001925.
57.
Purves D, Augustine GJ, Fitzpatrick D, et al. Neuroscience. 3rd ed. Sunderland, MA: Sinauer Associates, Inc.; 2004.
58.
Weightman A, Jenkins S, Pickard M, Chari D, Yang Y. Alignment of multiple glial cell populations in 3D nanofiber scaffolds: toward the development of multicellular implantable scaffolds for repair of neural injury. Nanomedicine. 2014;10(2):291–295.
59.
Mahairaki V, Lim SH, Christopherson GT, et al. Nanofiber matrices promote the neuronal differentiation of human embryonic stem cell-derived neural precursors in vitro. Tissue Eng Part A. 2011;17(5–6):855–863.
60.
Hoffman-Kim D, Mitchel JA, Bellamkonda RV. Topography, cell Response, and nerve regeneration. Annu Rev Biomed Eng. 2010;12:203–231.
61.
Lai B-Q, Wang J-M, Ling E-A, Wu J-L, Zeng Y-S. Graft of a tissue-engineered neural scaffold serves as a promising strategy to restore myelination after rat spinal cord transection. Stem Cells Dev. 2014; 23(8):910–921.
62.
Ellis-Behnke RG, Liang Y-X, You S-W, et al. 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.
63.
Liu C, Huang Y, Pang M, et al. Tissue-engineered regeneration of completely transected spinal cord using induced neural stem cells and gelatin-electrospun poly (lactide-co-glycolide)/polyethylene glycol scaffolds. PLoS One. 2015;10(3):e0117709.
64.
Yang Y, Wimpenny I, Ahearne M. Portable nanofiber meshes dictate cell orientation throughout three-dimensional hydrogels. Nanomedicine. 2011;7(2):131–136.
65.
Weightman AP, Pickard MR, Yang Y, Chari DM. An in vitro spinal cord injury model to screen neuroregenerative materials. Biomaterials. 2014;35(12):3756–3765.
66.
Puschmann TB, Pablo Y De, Zande C, et al. A novel method for three-dimensional culture of central nervous system neurons. Tissue Eng Part C Methods. 2014;20(6):485–493.
67.
Dumont RJ, Okonkwo DO, Verma S, et al. Acute spinal cord injury, part I: pathophysiologic mechanisms. Clinical Neuropharmacol. 2001;24(5):254–264.
68.
Thuret S, Moon LDF, Gage FH. Therapeutic interventions after spinal cord injury. Nature Reviews Neuroscience. 2006;7(8):628–643.
69.
Ray SK, Dixon CE, Banik NL. Molecular mechanisms in the pathogenesis of traumatic brain injury. Histol Histopathol. 2002;17(4):1137–1152.
70.
Onifer SM, Rabchevsky AG, Scheff SW. Rat models of traumatic spinal cord injury to assess motor recovery. ILAR J. 2007;48(4):385–395.
71.
Shibuya S, Yamamoto T, Itano T. Glial and axonal regeneration following spinal cord injury. Cell Adh Migr. 2009;3(1):99–106.
Journal of Neurorestoratology
Pages 123-131
Cite this article:
Kamudzandu M, Roach P, Fricker RA, et al. Nanofibrous scaffolds supporting optimal central nervous system regeneration: an evidence-based review. Journal of Neurorestoratology, 2015, 3(1): 123-131. https://doi.org/10.2147/JN.S70337

498

Views

15

Downloads

0

Crossref

8

Web of Science

0

Scopus

Altmetrics

Published: 02 December 2015
© 2015 The Author(s).

© 2015 Kamudzandu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. Permissions beyond the scope of the License are administered by Dove Medical Press Limited. Information on how to request permission may be found at: http://www.dovepress.com/permissions.php

Return