dc.contributor.author
Demko, Peter
dc.contributor.author
Hillebrandt, Karl H.
dc.contributor.author
Napierala, Hendrik
dc.contributor.author
Haep, Nils
dc.contributor.author
Tang, Peter
dc.contributor.author
Gassner, Joseph M. G. V.
dc.contributor.author
Kluge, Martin
dc.contributor.author
Everwien, Hannah
dc.contributor.author
Polenz, Dietrich
dc.contributor.author
Reutzel-Selke, Anja
dc.contributor.author
Raschzok, Nathanael
dc.contributor.author
Pratschke, Johann
dc.contributor.author
Sauer, Igor M.
dc.contributor.author
Struecker, Benjamin
dc.contributor.author
Dobrindt, Eva M.
dc.date.accessioned
2024-09-27T09:51:48Z
dc.date.available
2024-09-27T09:51:48Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/45060
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-44772
dc.description.abstract
Purpose: Artificial organs might serve as alternative solutions for whole organ transplantation. Decellularization of a liver provides a non-immunogenic matrix with the advantage of three afferent systems, the portal vein, the hepatic artery and the bile duct. This study aims to evaluate the recellularization of rat livers with islets of Langerhans via the bile duct and the portal vein for the comparison of different perfusion routes.
Methods: Rat livers were decellularized in a pressure-controlled perfusion manner and repopulated with intact isolated islets of Langerhans via either the portal vein or the bile duct.
Results: Repopulation via the portal vein showed islet clusters stuck within the vascular system demonstrated by ellipsoid borders of thick reticular tissue around the islet cluster in Azan staining. After recellularization via the bile duct, islets were distributed close to the vessels within the parenchymal space and without a surrounding reticular layer. Large clusters of islets had a diameter of up to 1000 mu m without clear shapes.
Conclusion: We demonstrated the bile duct to be superior to the portal vein for repopulation of a decellularized rat liver with islets of Langerhans. This technique may serve as a bioengineering platform to generate an implantable and functional endocrine neo-pancreas and provide scaffolds with the anatomic benefit of three afferent systems to facilitate co-population of cells.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Tissue engineering
en
dc.subject
Islets of Langerhans
en
dc.subject
Extracellular matrix
en
dc.subject
Decellularization
en
dc.subject
Recellularization
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Perfusion-Based Recellularization of Rat Livers with Islets of Langerhans
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1007/s40846-022-00697-5
dcterms.bibliographicCitation.journaltitle
Journal of Medical and Biological Engineering
dcterms.bibliographicCitation.number
2
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.pagestart
271
dcterms.bibliographicCitation.pageend
280
dcterms.bibliographicCitation.volume
42
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1609-0985
dcterms.isPartOf.eissn
2199-4757