The Viral Vector Core Facility is an integral component of the UNC Gene Therapy Center. It has been in operation for over 8 years and has maintained an exponential level of production growth over this time. This growth has been accomplished by rapid incorporation of new technological developments as they become available, and by a commitment to making the proceeds of these technologies as widely accessible to researchers as possible. The pursuit of these goals will continue within the proposed research program. Among the new technologies and services to be added to the Vector Core will be the production of helper-dependent adenovirus vectors (HD-Ad), chimeric capsid adeno-associated virus vectors (chAAV), double-strand (or self-complementary) adeno-associated virus vectors (dsAAV), paramyxovirus vectors, and large-scale plasmid preparations to facilitate the production of experimental laboratory-scale stocks of viral vectors. Each of these services will dovetail with the specific needs and research interests of the MTCC investigators and their cystic fibrosis and metabolic disease research programs. Some of these new services will also play an important supporting role in the proposed pilot and feasibility studies, i.e., production of chAAV (McCarty, P.I.) and paramyxovirus vectors (Pickles, P.I.).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK065988-03
Application #
7222645
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
3
Fiscal Year
2006
Total Cost
$150,380
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Ghaedi, Mahboobe; Le, Andrew V; Hatachi, Go et al. (2018) Bioengineered lungs generated from human iPSCs-derived epithelial cells on native extracellular matrix. J Tissue Eng Regen Med 12:e1623-e1635
Livraghi-Butrico, Alessandra; Wilkinson, Kristen J; Volmer, Allison S et al. (2018) Lung disease phenotypes caused by overexpression of combinations of ?-, ?-, and ?-subunits of the epithelial sodium channel in mouse airways. Am J Physiol Lung Cell Mol Physiol 314:L318-L331
Chen, Gang; Volmer, Allison S; Wilkinson, Kristen J et al. (2018) Role of Spdef in the Regulation of Muc5b Expression in the Airways of Naive and Mucoobstructed Mice. Am J Respir Cell Mol Biol 59:383-396
Goralski, Jennifer L; Wu, Dan; Thelin, William R et al. (2018) The in vitro effect of nebulised hypertonic saline on human bronchial epithelium. Eur Respir J 51:
Hussain, Shah S; George, Shebin; Singh, Shashi et al. (2018) A Small Molecule BH3-mimetic Suppresses Cigarette Smoke-Induced Mucous Expression in Airway Epithelial Cells. Sci Rep 8:13796
Agostini, Maria L; Andres, Erica L; Sims, Amy C et al. (2018) Coronavirus Susceptibility to the Antiviral Remdesivir (GS-5734) Is Mediated by the Viral Polymerase and the Proofreading Exoribonuclease. MBio 9:
Tomati, Valeria; Caci, Emanuela; Ferrera, Loretta et al. (2018) Thymosin ?-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia. JCI Insight 3:
Kim, Christine Seulki; Ahmad, Saira; Wu, Tongde et al. (2018) SPLUNC1 is an allosteric modulator of the epithelial sodium channel. FASEB J 32:2478-2491
Polineni, Deepika; Dang, Hong; Gallins, Paul J et al. (2018) Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease Severity. Am J Respir Crit Care Med 197:79-93
Abdullah, Lubna H; Coakley, Raymond; Webster, Megan J et al. (2018) Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia. Am J Respir Crit Care Med 197:481-491

Showing the most recent 10 out of 133 publications