Sv40 transfected human anterior cruciate ligament derived ligamentocytes—suitable as a human in vitro model for ligament reconstruction?

dc.bibliographicCitation.firstPage593eng
dc.bibliographicCitation.issue2eng
dc.bibliographicCitation.journalTitleInternational journal of molecular scienceseng
dc.bibliographicCitation.volume21eng
dc.contributor.authorSchulze-Tanzil, Gundula
dc.contributor.authorArnold, Philipp
dc.contributor.authorGögele, Clemens
dc.contributor.authorHahn, Judith
dc.contributor.authorBreier, Annette
dc.contributor.authorMeyer, Michael
dc.contributor.authorKohl, Benjamin
dc.contributor.authorSchröpfer, Michaela
dc.contributor.authorSchwarz, Silke
dc.date.accessioned2021-11-05T09:14:37Z
dc.date.available2021-11-05T09:14:37Z
dc.date.issued2020
dc.description.abstractCultured human primary cells have a limited lifespan undergoing dedifferentiation or senescence. Anterior cruciate ligaments (ACL) are hypocellular but tissue engineering (TE) requires high cell numbers. Simian virus (SV) 40 tumor (T) antigen expression could extend the lifespan of cells. This study aimed to identify cellular changes induced by SV40 expression in human ACL ligamentocytes by comparing them with non-transfected ligamentocytes and tissue of the same donor to assess their applicability as TE model. Human ACL ligamentocytes (40-year-old female donor after ACL rupture) were either transfected with a SV40 plasmid or remained non-transfected (control) before monitored for SV40 expression, survival, and DNA content. Protein expression of cultured ligamentocytes was compared with the donor tissue. Ligamentocyte spheroids were seeded on scaffolds embroidered either from polylactic acid (PLA) threads solely or combined PLA and poly (L-lactide-co-e-caprolactone) (P(LA-CL)) threads. These scaffolds were further functionalized with fluorination and fibrillated collagen foam. Cell distribution and survival were monitored for up to five weeks. The transfected cells expressed the SV40 antigen throughout the entire observation time, but often exhibited random and incomplete cell divisions with significantly more dying cells, significantly more DNA and more numerous nucleoli than controls. The expression profile of non-transfected and SV40-positive ligamentocytes was similar. In contrast to controls, SV40-positive cells formed larger spheroids, produced less vimentin and focal adhesions and died on the scaffolds after 21 d. Functionalized scaffolds supported human ligamentocyte growth. SV40 antigen expressing ligamentocytes share many properties with their non-transfected counterparts suggesting them as a model, however, applicability for TE is limited. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/7186
dc.identifier.urihttps://doi.org/10.34657/6233
dc.language.isoengeng
dc.publisherBasel : Molecular Diversity Preservation Internationaleng
dc.relation.doihttps://doi.org/10.3390/ijms21020593
dc.relation.essn1422-0067
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc570eng
dc.subject.ddc540eng
dc.subject.otherAnterior cruciate ligamenteng
dc.subject.otherEmbroidered scaffoldeng
dc.subject.otherLigamentocyteseng
dc.subject.otherP(LA-CL)eng
dc.subject.otherPLAeng
dc.subject.otherSV40eng
dc.subject.otherTissue engineeringeng
dc.titleSv40 transfected human anterior cruciate ligament derived ligamentocytes—suitable as a human in vitro model for ligament reconstruction?eng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectBiowissensschaften/Biologieeng
wgl.typeZeitschriftenartikeleng
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