The Cells and Tissue Core was formulated to provide airway cells for use in animal models and in vitro gene transfer experiments. The use of these models is required for understanding the pathophysiology of CF and for studies of CFTR gene transfer to airway epithelia. Overall objectives: The purpose of this core is to provide centralized access to non-CF and CF tissue and airway cells used for model systems in the analysis of gene transfer to the airway and pathophysiology in CF. The main responsibilities for the Core will include. 1. Acquisition of normal and CF tissue; 2. Generation of in vitro models of human airway epithelia; 3. Production of cultured cells for investigators in the Center; 4. Characterization of cultured and native epithelia; 5. Research and development of new methods for the culture and study of airway epithelia; 6. Teaching investigators the methods for developing in vitro model systems; 7. Record keeping relevant to tissue acquisition and cell culture; 8. Create a repository of airway tissue and primary cell cultures from the Regional Midwest CF Lung Tissue Acquisition Program; 9. Electrophysiologic analysis of CF airway epithelia transduced by gene delivery vectors; 10. Bronchoscopic acquisition and processing of human alveolar macrophages for distribution among the members of the Center. A successful Cell Culture Core will provide the models and expertise to the growing community of investigators from different areas, and allow them to focus their unique expertise in the development of CF gene transfer.

Project Start
2000-09-01
Project End
2001-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
3
Fiscal Year
2000
Total Cost
$143,268
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Reznikov, Leah R; Meyerholz, David K; Kuan, Shin-Ping et al. (2018) Solitary Cholinergic Stimulation Induces Airway Hyperreactivity and Transcription of Distinct Pro-inflammatory Pathways. Lung 196:219-229
Martinez, Carlos H; Li, Sara X; Hirzel, Andrew J et al. (2018) Alveolar eosinophilia in current smokers with chronic obstructive pulmonary disease in the SPIROMICS cohort. J Allergy Clin Immunol 141:429-432
Ash, Samuel Y; Rahaghi, Farbod N; Come, Carolyn E et al. (2018) Pruning of the Pulmonary Vasculature in Asthma. The Severe Asthma Research Program (SARP) Cohort. Am J Respir Crit Care Med 198:39-50
Hua, Xiaoyang; Vijay, Rahul; Channappanavar, Rudragouda et al. (2018) Nasal priming by a murine coronavirus provides protective immunity against lethal heterologous virus pneumonia. JCI Insight 3:
Meyerholz, David K; Sieren, Jessica C; Beck, Amanda P et al. (2018) Approaches to Evaluate Lung Inflammation in Translational Research. Vet Pathol 55:42-52
Schmidt, Megan E; Knudson, Cory J; Hartwig, Stacey M et al. (2018) Memory CD8 T cells mediate severe immunopathology following respiratory syncytial virus infection. PLoS Pathog 14:e1006810
Hornick, Emma E; Banoth, Balaji; Miller, Ann M et al. (2018) Nlrp12 Mediates Adverse Neutrophil Recruitment during Influenza Virus Infection. J Immunol 200:1188-1197
Abou Alaiwa, Mahmoud H; Launspach, Jan L; Grogan, Brenda et al. (2018) Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis. JCI Insight 3:
Lynch, Thomas J; Anderson, Preston J; Rotti, Pavana G et al. (2018) Submucosal Gland Myoepithelial Cells Are Reserve Stem Cells That Can Regenerate Mouse Tracheal Epithelium. Cell Stem Cell 22:653-667.e5
Kang, Chen; Xie, Litao; Gunasekar, Susheel K et al. (2018) SWELL1 is a glucose sensor regulating ?-cell excitability and systemic glycaemia. Nat Commun 9:367

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