Por favor, use este identificador para citar o enlazar este Item:http://hdl.handle.net/20.500.12105/9808
Título
New Methods for Disease Modeling Using Lentiviral Vectors
Autor(es)
Fecha de publicación
2018-10
Cita
Trends Mol Med. 2018; 24(10):852-37
Idioma
Inglés
Tipo de documento
journal article
Resumen
Lentiviral vectors (LVs) transduce quiescent cells and provide stable integration to maintain transgene expression. Several approaches have been adopted to optimize LV safety profiles. Similarly, LV targeting has been tailored through strategies including the modification of envelope components, the use of specific regulatory elements, and the selection of appropriate administration routes. Models of aortic disease based on a single injection of pleiotropic LVs have been developed that efficiently transduce the three aorta layers in wild type mice. This approach allows the dissection of pathways involved in aortic aneurysm formation and the identification of targets for gene therapy in aortic diseases. LVs provide a fast, efficient, and affordable alternative to genetically modified mice to study disease mechanisms and develop therapeutic tools.
Palabras clave
MESH
ADAMTS1 Protein | Animals | Aortic Aneurysm | Clinical Trials as Topic | Disease Models, Animal | Gene Expression Regulation | Genetic Therapy | Genetic Vectors | Humans | Immunity, Innate | Lentivirus | Mice | Patient Safety | RNA, Small Interfering | Transduction, Genetic | Transgenes
DOI
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