Publication:
Chitosan channels stuffed with mesenchyme originated stem/progenitor cells for renovate axonal regeneration in complete spinal cord transection

dc.contributor.coauthorÇakıcı, Nazlı
dc.contributor.coauthorBozkurt, Gökhan
dc.contributor.coauthorPuralı, Nuhan
dc.contributor.coauthorDenkbaş, Emir Baki
dc.contributor.coauthorKorkusuz, Petek
dc.contributor.coauthorUçkan Çetinkaya, Duygu
dc.contributor.kuauthorBaşak, Ahmet Tulgar
dc.contributor.kuprofileDoctor
dc.contributor.unitKoç University Hospital
dc.date.accessioned2024-11-09T13:48:21Z
dc.date.issued2021
dc.description.abstractAim: to examine the implantation of chitosan channels stuffed with mesenchyme-originated stem/progenitor cells (MSPCs) derived from adult rats in a spinal cord transection model. The level of axonal regeneration, the effect of chitosan channels on the survival of MSPCs, and the functional recovery results were also evaluated. Material and methods: chitosan channels stuffed with MSPCs were implanted at the level of T8 in a transected rat spinal cord. MSPCs were harvested from the pelvic bone marrow of adult rats, and the MSPC-chitosan channel group was compared with three control groups. The axonal regeneration capacity, the effect of chitosan channels on the survival of MSPCs, and the functional recovery results were compared among four groups. The survival of MSPCs was evaluated using histopathological techniques and electron microscopy, axonal regeneration/germination was evaluated by confocal microscopy, and locomotor function was assessed for 4 weeks using the Basso, Beattie, and Bresnahan locomotor score. Results: the MSPC-chitosan channel group exhibited enhanced survival of transplanted MSPCs compared with MSPCs transplanted directly into the lesion cavity, although no significant difference was detected in locomotor function between the treatment and control groups. The MSPC-chitosan channel group demonstrated thicker myelination of axons than the other groups. Conclusion: chitosan channels promoted the survival of transplanted MSPCs and created a tissue bridge after complete spinal cord transection. They also induced axonal regeneration and germination. No significant improvement in functional recovery was found between the groups.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue2
dc.description.openaccessYES
dc.description.publisherscopeNational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipHacettepe University
dc.description.versionPublisher version
dc.description.volume31
dc.formatpdf
dc.identifier.doi10.5137/1019-5149.JTN.29489-20.5
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR02824
dc.identifier.issn1019-5149
dc.identifier.linkhttps://doi.org/10.5137/1019-5149.JTN.29489-20.5
dc.identifier.quartileQ4
dc.identifier.scopus2-s2.0-85103474500
dc.identifier.urihttps://hdl.handle.net/20.500.14288/3817
dc.identifier.wos631709500006
dc.keywordsMesenchyme-originated stem/progenitor cells
dc.keywordsAxonal regeneration
dc.keywordsChitosan channel
dc.keywordsComplete spinal cord transection
dc.languageEnglish
dc.publisherTurkish Neurosurgical Society
dc.relation.grantnoNA
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9475
dc.sourceTurkish Neurosurgery
dc.subjectClinical neurology
dc.subjectSurgery
dc.titleChitosan channels stuffed with mesenchyme originated stem/progenitor cells for renovate axonal regeneration in complete spinal cord transection
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorBaşak, Ahmet Tulgar

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