Development of Biological Meniscus Scaffold: Decellularization Method and Recellularization With Meniscal Cell Population Derived From Mesenchymal Stem Cells

dc.contributor.author Kara, Aylin
dc.contributor.author Koçtürk, Semra
dc.contributor.author Bilici, Gökçen
dc.contributor.author Havıtçıoğlu, Hasan
dc.date.accessioned 2021-11-06T09:49:31Z
dc.date.available 2021-11-06T09:49:31Z
dc.date.issued 2021
dc.description.abstract Tissue engineering approaches which include a combination of cells and scaffold materials provide an alternative treatment for meniscus regeneration. Decellularization and recellularization techniques are potential treatment options for transplantation. Maintenance of the ultrastructure composition of the extracellular matrix and repopulation with cells are important factors in constructing a biological scaffold and eliminating immunological reactions. The aim of the study is to develop a method to obtain biological functional meniscus scaffolds for meniscus regeneration. For this purpose, meniscus tissue was decellularized by our modified method, a combination of physical, chemical, and enzymatic methods and then recellularized with a meniscal cell population composed of fibroblasts, chondrocytes and fibrochondrocytes that obtained from mesenchymal stem cells. Decellularized and recellularized meniscus scaffolds were analysed biochemically, biomechanically and histologically. Our results revealed that cellular components of the meniscus were successfully removed by preserving collagen and GAG structures without any significant loss in biomechanical properties. Recellularization results showed that the meniscal cells were localized in the empty lacuna on the decellularized meniscus, and also well distributed and proliferated consistently during the cell culture period (p < 0.05). Furthermore, a high amount of DNA, collagen, and GAG contents (p < 0.05) were obtained with the meniscal cell population in recellularized meniscus tissue. The study demonstrates that our decellularization and recellularization methods were effective to develop a biological functional meniscus scaffold and can mimic the meniscus tissue with structural and biochemical features. We predict that the obtained biological meniscus scaffolds may provide avoidance of adverse immune reactions and an appropriate microenvironment for allogeneic or xenogeneic recipients in the transplantation process. Therefore, as a promising candidate, the obtained biological meniscus scaffolds might be verified with a transplantation experiment. en_US
dc.description.sponsorship The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by Dokuz Eylul University, Department of Scientific Research Project (2015.KB. SAG.039). en_US
dc.identifier.doi 10.1177/0885328220981189
dc.identifier.issn 0885-3282
dc.identifier.issn 1530-8022
dc.identifier.scopus 2-s2.0-85099460380
dc.identifier.uri https://doi.org/10.1177/0885328220981189
dc.identifier.uri https://hdl.handle.net/11147/11442
dc.language.iso en en_US
dc.publisher SAGE Publications en_US
dc.relation.ispartof Journal of Biomaterials Applications en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Meniscus en_US
dc.subject Decellularization en_US
dc.subject Recellularization en_US
dc.subject Mesenchymal stem cells en_US
dc.subject Fibrochondrocytes en_US
dc.subject Tissue engineering en_US
dc.title Development of Biological Meniscus Scaffold: Decellularization Method and Recellularization With Meniscal Cell Population Derived From Mesenchymal Stem Cells en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id 0000-0001-8302-913X
gdc.author.id 0000-0001-7528-1845
gdc.author.id 0000-0001-8302-913X en_US
gdc.author.id 0000-0001-7528-1845 en_US
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Bioengineering en_US
gdc.description.endpage 1207 en_US
gdc.description.issue 9 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 1192 en_US
gdc.description.volume 35 en_US
gdc.description.wosquality Q3
gdc.identifier.openalex W3120956043
gdc.identifier.pmid 33444085
gdc.identifier.wos WOS:000631243600001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.diamondjournal false
gdc.oaire.impulse 9.0
gdc.oaire.influence 2.9625848E-9
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gdc.oaire.keywords Compressive Strength
gdc.oaire.keywords Tissue Engineering
gdc.oaire.keywords Tissue Scaffolds
gdc.oaire.keywords Cell Culture Techniques
gdc.oaire.keywords Cell Differentiation
gdc.oaire.keywords Mesenchymal Stem Cells
gdc.oaire.keywords Biomechanical Phenomena
gdc.oaire.keywords Extracellular Matrix
gdc.oaire.keywords Animals
gdc.oaire.keywords Female
gdc.oaire.keywords Meniscus
gdc.oaire.keywords Collagen
gdc.oaire.keywords Rabbits
gdc.oaire.keywords Biomarkers
gdc.oaire.keywords Cell Proliferation
gdc.oaire.popularity 1.0384564E-8
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gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.collaboration National
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gdc.openalex.normalizedpercentile 0.86
gdc.openalex.toppercent TOP 10%
gdc.opencitations.count 13
gdc.plumx.crossrefcites 10
gdc.plumx.mendeley 23
gdc.plumx.pubmedcites 5
gdc.plumx.scopuscites 14
gdc.scopus.citedcount 14
gdc.wos.citedcount 14
relation.isAuthorOfPublication.latestForDiscovery eff72266-3dea-4765-93f1-358831ec642a
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