Cell cultures are instrumental for studying basic and applied aspects of gene therapy for cytic fibrosis (CF). Human airway epithelial cells maintained at an air-liquid interface display mucociliary differentiation similar to the in vivo epithelium. These cells faithfully reproduce the high resistance to vectors, characteristic of the native mucosa, providing a strong platform for pre-clinical studies to address issues crucial to the success of gene therapy for CF. A Tissue Procurement and Cell Culture Core was established at the University of North Carolina (UNC) in 1984, under the auspices of the CF Foundation, to provide standardized cell cultures to CF researchers. The Core has supported UNC Gene Therapy for CF projects since 1993 and has increased its output and capabilities to meet growing research demands. The Core routinely makes available cells and media that are unavailable and/or prohibitively expensive if purchased commercially. The present application will provide continuity in the supply of human airway epithelial cell cultures to UNC Gene Therapy for Cystic Fibrosis Program Project investigators by providing the followingspecific functions: 1) Obtain airway tissues from normal, CF and disease control humans as the source for primary cells, for acute ex vivo experiments, protein and RNA isolation, immunostaining and in situ hybridization. Characterize donors while protecting confidentiality. 2) Isolate primary epithelial cells from excised human airways. Prepare and maintain primary epithelial cell cultures. Provide support for preparation of well differentiated airway epithelial cultures from passaged or cryopreserved primary human cells. Optimize culture conditions to replicate gene expression, morphological differentiation, and physiologic functions of airways as evidenced by rotational mucus transport and regulation of the airway surface liquid (ASL) layer. Through these functions, and in conjunction with other Cores in this application, the CellCulture Core will support research towards the development of safe and effective gene therapy for CF.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL051818-11
Application #
6956040
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2004-08-20
Project End
2009-06-30
Budget Start
2004-08-20
Budget End
2005-06-30
Support Year
11
Fiscal Year
2004
Total Cost
$101,859
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Goudy, Kevin S; Johnson, Mark C; Garland, Alaina et al. (2011) Inducible adeno-associated virus-mediated IL-2 gene therapy prevents autoimmune diabetes. J Immunol 186:3779-86
Li, Wuping; Zhang, Liqun; Wu, Zhijian et al. (2011) AAV-6 mediated efficient transduction of mouse lower airways. Virology 417:327-33
Zhang, Liqun; Collins, Peter L; Lamb, Robert A et al. (2011) Comparison of differing cytopathic effects in human airway epithelium of parainfluenza virus 5 (W3A), parainfluenza virus type 3, and respiratory syncytial virus. Virology 421:67-77
Johnson, Jarrod S; Gentzsch, Martina; Zhang, Liqun et al. (2011) AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosis. PLoS Pathog 7:e1002053
Johnson, Jarrod S; Li, Chengwen; DiPrimio, Nina et al. (2010) Mutagenesis of adeno-associated virus type 2 capsid protein VP1 uncovers new roles for basic amino acids in trafficking and cell-specific transduction. J Virol 84:8888-902
Kwilas, Anna R; Yednak, Mark A; Zhang, Liqun et al. (2010) Respiratory syncytial virus engineered to express the cystic fibrosis transmembrane conductance regulator corrects the bioelectric phenotype of human cystic fibrosis airway epithelium in vitro. J Virol 84:7770-81
Mitchell, Angela M; Nicolson, Sarah C; Warischalk, Jayme K et al. (2010) AAV's anatomy: roadmap for optimizing vectors for translational success. Curr Gene Ther 10:319-340
Zhang, Liqun; Limberis, Maria P; Thompson, Catherine et al. (2010) ?-Fetoprotein gene delivery to the nasal epithelium of nonhuman primates by human parainfluenza viral vectors. Hum Gene Ther 21:1657-64
Zhang, Liqun; Button, Brian; Gabriel, Sherif E et al. (2009) CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium. PLoS Biol 7:e1000155
Li, Wuping; Zhang, Liqun; Johnson, Jarrod S et al. (2009) Generation of novel AAV variants by directed evolution for improved CFTR delivery to human ciliated airway epithelium. Mol Ther 17:2067-77

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