(This Core was previously named the Gene Transfer, Targeting, and Therapeutics Core) Viral vectors are commonly used to deliver genetic material to targeted cells, both in vitro and in vivo. They also represent attractive candidates for in vivo gene therapy. However, there are significant safety concerns when working with and producing research grade viral vectors. These safety issues are compounded when individual research laboratories are tasked with establishing and maintaining their own safety infrastructure and protocols. To address these concerns, the Salk Institute has established a centralized resource, namely the Viral Vector Core. The Core produces and maintains an extensive library of commonly-used stock viral vectors. In addition, the Core offers custom design and production services for multiple types of viral vectors, including lentivirus, retrovirus, adenovirus, adeno-associated virus, G-deleted rabies, and vesicular stomatitis virus. Finally, the Core provides expert consultation services, helping researchers identify the viral vector tool best suited for their stated objectives, and teaching investigators how to safely handle and use viral vector technologies. Salk Cancer Center members have utilized both the custom and stock vector production services, as well as the NanoSight Particle Tracker, which is used to visualize and count nanoparticles such as viruses and exosomes. To help Salk Cancer Center members innovate new experimental tools and potential therapies, the Viral Vector Core constantly seeks to introduce novel viral vector technologies. Recent advances in viral vector design have produced new AAV capsids and lentivirus/retrovirus envelope proteins with enhanced infection and trafficking characteristics. The Core has incorporated these novel tools into Core offerings, making them available to Cancer Center researchers. Core staff have also introduced a self- inactivating rabies virus that has markedly less cytotoxicity, thus improving the utility of these vectors.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014195-46
Application #
9634007
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
46
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
078731668
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Lewis Jr, Tommy L; Kwon, Seok-Kyu; Lee, Annie et al. (2018) MFF-dependent mitochondrial fission regulates presynaptic release and axon branching by limiting axonal mitochondria size. Nat Commun 9:5008
Eichner, Lillian J; Brun, Sonja N; Herzig, Sébastien et al. (2018) Genetic Analysis Reveals AMPK Is Required to Support Tumor Growth in Murine Kras-Dependent Lung Cancer Models. Cell Metab :
Dravis, Christopher; Chung, Chi-Yeh; Lytle, Nikki K et al. (2018) Epigenetic and Transcriptomic Profiling of Mammary Gland Development and Tumor Models Disclose Regulators of Cell State Plasticity. Cancer Cell 34:466-482.e6
Zarrinpar, Amir; Chaix, Amandine; Xu, Zhenjiang Z et al. (2018) Antibiotic-induced microbiome depletion alters metabolic homeostasis by affecting gut signaling and colonic metabolism. Nat Commun 9:2872
Ramaswamy, Suvasini; Tonnu, Nina; Menon, Tushar et al. (2018) Autologous and Heterologous Cell Therapy for Hemophilia B toward Functional Restoration of Factor IX. Cell Rep 23:1565-1580
Hsu, Cynthia L; Lee, Elian X; Gordon, Kara L et al. (2018) MAP4K3 mediates amino acid-dependent regulation of autophagy via phosphorylation of TFEB. Nat Commun 9:942
Sonntag, Tim; Vaughan, Joan M; Montminy, Marc (2018) 14-3-3 proteins mediate inhibitory effects of cAMP on salt-inducible kinases (SIKs). FEBS J 285:467-480
Herzig, Sébastien; Shaw, Reuben J (2018) AMPK: guardian of metabolism and mitochondrial homeostasis. Nat Rev Mol Cell Biol 19:121-135
Sweeney, Lora B; Bikoff, Jay B; Gabitto, Mariano I et al. (2018) Origin and Segmental Diversity of Spinal Inhibitory Interneurons. Neuron 97:341-355.e3
Hartmann, Phillipp; Hochrath, Katrin; Horvath, Angela et al. (2018) Modulation of the intestinal bile acid/farnesoid X receptor/fibroblast growth factor 15 axis improves alcoholic liver disease in mice. Hepatology 67:2150-2166

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