dc.contributor.author
Kotnik, Katarina
dc.contributor.author
Popova, Elena
dc.contributor.author
Todiras, Mihail
dc.contributor.author
Mori, Marcelo A.
dc.contributor.author
Alenina, Natalia
dc.contributor.author
Seibler, Jost
dc.contributor.author
Bader, Michael
dc.date.accessioned
2018-06-08T03:22:02Z
dc.date.available
2015-09-23T07:01:58.426Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15016
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19204
dc.description.abstract
The rat is an important animal model in biomedical research, but gene
targeting technology is not established for this species. Therefore, we aimed
to produce transgenic knockdown rats using shRNA technology and pronuclear
microinjection. To this purpose, we employed a tetracycline-inducible shRNA
expression system targeting the insulin receptor (IR). Doxycycline (DOX)
treatment of the resulting transgenic rats led to a dose-dependent and
reversible increase in blood glucose caused by ubiquitous inhibition of IR
expression and signalling. We could neither detect an interferon response nor
disturbances in microRNA processing after DOX treatment excluding toxic
effects of shRNA expression. Low dose DOX treatment induced a chronic state of
diabetes mellitus. In conclusion, we have developed a technology which allows
the specific, inducible, and reversible suppression of any gene of interest in
the rat. Our first transgenic rat line generated with this method represents
an inducible model for diabetes mellitus.
en
dc.rights.uri
http://creativecommons.org/licenses/by/2.5/
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Inducible Transgenic Rat Model for Diabetes Mellitus Based on shRNA-Mediated
Gene Knockdown
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
PLoS ONE. - 4 (2009), 4, Artikel Nr. e5124
dcterms.bibliographicCitation.doi
10.1371/journal.pone.0005124
dcterms.bibliographicCitation.url
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0005124
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.mycore.fudocsId
FUDOCS_document_000000023152
refubium.note.author
Der Artikel wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000005428
dcterms.accessRights.openaire
open access