dc.contributor.author
Hiller, Thomas
dc.contributor.author
Berg, Johanna
dc.contributor.author
Elomaa, Laura
dc.contributor.author
Röhrs, Viola
dc.contributor.author
Ullah, Imran
dc.contributor.author
Schaar, Katrin
dc.contributor.author
Dietrich, Ann-Christin
dc.contributor.author
Al-Zeer, Munir A.
dc.contributor.author
Kurtz, Andreas
dc.contributor.author
Hocke, Andreas C.
dc.contributor.author
Hippenstiel, Stefan
dc.contributor.author
Fechner, Henry
dc.contributor.author
Weinhart, Marie
dc.contributor.author
Kurreck, Jens
dc.date.accessioned
2018-10-24T15:10:45Z
dc.date.available
2018-10-24T15:10:45Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/23114
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-908
dc.description.abstract
Bioprinting is a novel technology that may help to overcome limitations associated with two-dimensional (2D) cell cultures and animal experiments, as it allows the production of three-dimensional (3D) tissue models composed of human cells. The present study describes the optimization of a bioink composed of alginate, gelatin and human extracellular matrix (hECM) to print human HepaRG liver cells with a pneumatic extrusion printer. The resulting tissue model was tested for its suitability for the study of transduction by an adeno-associated virus (AAV) vector and infection with human adenovirus 5 (hAdV5). We found supplementation of the basic alginate/gelatin bioink with 0.5 and 1 mg/mL hECM provides desirable properties for the printing process, the stability of the printed constructs, and the viability and metabolic functions of the printed HepaRG cells. The tissue models were efficiently transduced by AAV vectors of serotype 6, which successfully silenced an endogenous target (cyclophilin B) by means of RNA interference. Furthermore, the printed 3D model supported efficient adenoviral replication making it suitable to study virus biology and develop new antiviral compounds. We consider the approach described here paradigmatic for the development of 3D tissue models for studies including viral vectors and infectious viruses.
en
dc.format.extent
17 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
adeno-associated virus
en
dc.subject
transduction
en
dc.subject
extracellular matrix
en
dc.subject
organ models
en
dc.subject
gene silencing
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie
dc.title
Generation of a 3D Liver Model Comprising Human Extracellular Matrix in an Alginate/Gelatin-Based Bioink by Extrusion Bioprinting for Infection and Transduction Studies
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
3129
dcterms.bibliographicCitation.doi
10.3390/ijms19103129
dcterms.bibliographicCitation.journaltitle
International Journal of Molecular Sciences
dcterms.bibliographicCitation.number
10
dcterms.bibliographicCitation.volume
19
dcterms.bibliographicCitation.url
https://doi.org/10.3390/ijms19103129
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1422-0067
dcterms.isPartOf.issn
1661-6596