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Verfasst von:Abel, Tobias [VerfasserIn]   i
 El Filali, Ebtisam [VerfasserIn]   i
 Waern, Johan [VerfasserIn]   i
 Schneider, Irene C. [VerfasserIn]   i
 Yuan, Qinggong [VerfasserIn]   i
 Münch, Robert C. [VerfasserIn]   i
 Hick, Meike [VerfasserIn]   i
 Warnecke, Gregor [VerfasserIn]   i
 Madrahimov, Nodir [VerfasserIn]   i
 Kontermann, Roland E. [VerfasserIn]   i
 Schüttrumpf, Jörg [VerfasserIn]   i
 Müller, Ulrike C. [VerfasserIn]   i
 Seppen, Jurgen [VerfasserIn]   i
 Ott, Michael [VerfasserIn]   i
 Buchholz, Christian J. [VerfasserIn]   i
Titel:Specific gene delivery to liver sinusoidal and artery endothelial cells
Verf.angabe:Tobias Abel, Ebtisam El Filali, Johan Waern, Irene C. Schneider, Qinggong Yuan, Robert C. Münch, Meike Hick, Gregor Warnecke, Nodir Madrahimov, Roland E. Kontermann, Jörg Schüttrumpf, Ulrike C. Müller, Jurgen Seppen, Michael Ott, and Christian J. Buchholz
E-Jahr:2013
Jahr:July 24, 2013
Umfang:9 S.
Teil:volume:122
 year:2013
 number:12
 pages:2030-2038
 extent:9
Fussnoten:Gesehen am 05.05.2021
Titel Quelle:Enthalten in: Blood
Ort Quelle:Washington, DC : American Society of Hematology, 1946
Jahr Quelle:2013
Band/Heft Quelle:122(2013), 12, Seite 2030-2038
ISSN Quelle:1528-0020
Abstract:Different types of endothelial cells (EC) fulfill distinct tasks depending on their microenvironment. ECs are therefore difficult to genetically manipulate ex vivo for functional studies or gene therapy. We assessed lentiviral vectors (LVs) targeted to the EC surface marker CD105 for in vivo gene delivery. The mouse CD105-specific vector, mCD105-LV, transduced only CD105-positive cells in primary liver cell cultures. Upon systemic injection, strong reporter gene expression was detected in liver where mCD105-LV specifically transduced liver sinusoidal ECs (LSECs) but not Kupffer cells, which were mainly transduced by nontargeted LVs. Tumor ECs were specifically targeted upon intratumoral vector injection. Delivery of the erythropoietin gene with mCD105-LV resulted in substantially increased erythropoietin and hematocrit levels. The human CD105-specific vector (huCD105-LV) transduced exclusively human LSECs in mice transplanted with human liver ECs. Interestingly, when applied at higher dose and in absence of target cells in the liver, huCD105-LV transduced ECs of a human artery transplanted into the descending mouse aorta. The data demonstrate for the first time targeted gene delivery to specialized ECs upon systemic vector administration. This strategy offers novel options to better understand the physiological functions of ECs and to treat genetic diseases such as those affecting blood factors.
DOI:doi:10.1182/blood-2012-11-468579
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1182/blood-2012-11-468579
 DOI: https://doi.org/10.1182/blood-2012-11-468579
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1757126546
Verknüpfungen:→ Zeitschrift

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