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dc.contributor.authorPanseri, Silvia
dc.contributor.authorCunha, Carla
dc.contributor.authorLowery, Joseph L.
dc.contributor.authorDel Carro, Ubaldo
dc.contributor.authorTaraballi, Francesca
dc.contributor.authorAmadio, Stefano
dc.contributor.authorVescovi, Angelo
dc.contributor.authorGelain, Fabrizio
dc.date.accessioned2010-09-29T20:14:17Z
dc.date.available2010-09-29T20:14:17Z
dc.date.issued2008-04
dc.date.submitted2007-08
dc.identifier.issn1472-6750
dc.identifier.urihttp://hdl.handle.net/1721.1/58768
dc.description.abstractBackground: Although many nerve prostheses have been proposed in recent years, in the case of consistent loss of nervous tissue peripheral nerve injury is still a traumatic pathology that may impair patient's movements by interrupting his motor-sensory pathways. In the last few decades tissue engineering has opened the door to new approaches;: however most of them make use of rigid channel guides that may cause cell loss due to the lack of physiological local stresses exerted over the nervous tissue during patient's movement. Electrospinning technique makes it possible to spin microfiber and nanofiber flexible tubular scaffolds composed of a number of natural and synthetic components, showing high porosity and remarkable surface/volume ratio. Results: In this study we used electrospun tubes made of biodegradable polymers (a blend of PLGA/PCL) to regenerate a 10-mm nerve gap in a rat sciatic nerve in vivo. Experimental groups comprise lesioned animals (control group) and lesioned animals subjected to guide conduits implantated at the severed nerve stumps, where the tubular scaffolds are filled with saline solution. Four months after surgery, sciatic nerves failed to reconnect the two stumps of transected nerves in the control animal group. In most of the treated animals the electrospun tubes induced nervous regeneration and functional reconnection of the two severed sciatic nerve tracts. Myelination and collagen IV deposition have been detected in concurrence with regenerated fibers. No significant inflammatory response has been found. Neural tracers revealed the re-establishment of functional neuronal connections and evoked potential results showed the reinnervation of the target muscles in the majority of the treated animals. Conclusion: Corroborating previous works, this study indicates that electrospun tubes, with no additional biological coating or drug loading treatment, are promising scaffolds for functional nervous regeneration. They can be knitted in meshes and various frames depending on the cytoarchitecture of the tissue to be regenerated. The versatility of this technique gives room for further scaffold improvements, like tuning the mechanical properties of the tubular structure or providing biomimetic functionalization. Moreover, these guidance conduits can be loaded with various fillers like collagen, fibrin, or self-assembling peptide gels or loaded with neurotrophic factors and seeded with cells. Electrospun scaffolds can also be synthesized in different micro-architectures to regenerate lesions in other tissues like skin and bone.en_US
dc.description.sponsorshipFondazione Cariploen_US
dc.description.sponsorshipNicolas G. and Dorothea K. Dumbros Scholarship and Fellowship Funden_US
dc.description.sponsorshipUnited States. Army (contract DAAD-19-02-D-0002)en_US
dc.description.sponsorshipSixth Framework Programme (European Commission)en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/1472-6750-8-39en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleElectrospun micro- and nanofiber tubes for functional nervous regeneration in sciatic nerve transectionsen_US
dc.typeArticleen_US
dc.identifier.citationBMC Biotechnology. 2008 Apr 11;8(1):39en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Soldier Nanotechnologiesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorLowery, Joseph L.
dc.relation.journalBMC Biotechnologyen_US
dc.eprint.versionFinal published versionen_US
dc.identifier.pmid18405347
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2010-09-03T16:19:17Z
dc.language.rfc3066en
dc.rights.holderPanseri et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsPanseri, Silvia; Cunha, Carla; Lowery, Joseph; Del Carro, Ubaldo; Taraballi, Francesca; Amadio, Stefano; Vescovi, Angelo; Gelain, Fabrizioen
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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