Biomaterial based strategies to reconstruct the nigrostriatal pathway in organotypic slice co-cultures

dc.bibliographicCitation.firstPage250eng
dc.bibliographicCitation.journalTitleActa Biomaterialiaeng
dc.bibliographicCitation.lastPage262eng
dc.bibliographicCitation.volume121eng
dc.contributor.authorUcar, Buket
dc.contributor.authorKajtez, Janko
dc.contributor.authorFoidl, Bettina M.
dc.contributor.authorEigel, Dimitri
dc.contributor.authorWerner, Carsten
dc.contributor.authorLong, Katherine R.
dc.contributor.authorEmnéus, Jenny
dc.contributor.authorBizeau, Joëlle
dc.contributor.authorLomora, Mihai
dc.contributor.authorPandit, Abhay
dc.contributor.authorNewland, Ben
dc.contributor.authorHumpel, Christian
dc.date.accessioned2021-09-02T11:14:10Z
dc.date.available2021-09-02T11:14:10Z
dc.date.issued2021
dc.description.abstractProtection or repair of the nigrostriatal pathway represents a principal disease-modifying therapeutic strategy for Parkinson's disease (PD). Glial cell line-derived neurotrophic factor (GDNF) holds great therapeutic potential for PD, but its efficacious delivery remains difficult. The aim of this study was to evaluate the potential of different biomaterials (hydrogels, microspheres, cryogels and microcontact printed surfaces) for reconstructing the nigrostriatal pathway in organotypic co-culture of ventral mesencephalon and dorsal striatum. The biomaterials (either alone or loaded with GDNF) were locally applied onto the brain co-slices and fiber growth between the co-slices was evaluated after three weeks in culture based on staining for tyrosine hydroxylase (TH). Collagen hydrogels loaded with GDNF slightly promoted the TH+ nerve fiber growth towards the dorsal striatum, while GDNF loaded microspheres embedded within the hydrogels did not provide an improvement. Cryogels alone or loaded with GDNF also enhanced TH+ fiber growth. Lines of GDNF immobilized onto the membrane inserts via microcontact printing also significantly improved TH+ fiber growth. In conclusion, this study shows that various biomaterials and tissue engineering techniques can be employed to regenerate the nigrostriatal pathway in organotypic brain slices. This comparison of techniques highlights the relative merits of different technologies that researchers can use/develop for neuronal regeneration strategies. © 2020eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/6665
dc.identifier.urihttps://doi.org/10.34657/5712
dc.language.isoengeng
dc.publisherAmsterdam [u.a.] : Elseviereng
dc.relation.doihttps://doi.org/10.1016/j.actbio.2020.11.035
dc.relation.essn1878-7568
dc.relation.issn1742-7061
dc.rights.licenseCC BY-NC-ND 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/eng
dc.subject.ddc530eng
dc.subject.otherCryogeleng
dc.subject.otherGDNFeng
dc.subject.otherHydrogeleng
dc.subject.otherMicrocontact printingeng
dc.subject.otherNigrostriatal pathway regenerationeng
dc.subject.otherOrganotypic brain sliceseng
dc.titleBiomaterial based strategies to reconstruct the nigrostriatal pathway in organotypic slice co-cultureseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectPhysikeng
wgl.typeZeitschriftenartikeleng
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