(Cells and Tissue Core - Core 5) The Cells and Tissue Core was established to provide well-differentiated epithelial models for studies on the pathophysiology of cystic fibrosis (CF) and for molecular and gene therapy experiments. The Cells and Tissue Core mission is to advance CF research within the scope of the National Institute of Diabetes and Digestive and Kidney Diseases. CF affects multiple organs that result in digestive diseases, liver diseases, nutritional disorders, diabetes, and lung disease. These disorders affect people's health and quality of life. The Core achieves this mission by providing relevant models and technical expertise to investigators, developing new in vitro models and approaches, training investigators, and attracting new investigators to CF research and aiding their development. The goals of the Cells and Tissue Core are to collect, process and maintain a human tissue biobank of gallbladder, intestine, pancreas, vas deferens, kidney, and lung specimens, in collaboration with the Clinical Core (Core-6). We will also generate in vitro models of these same organs from humans, pigs, ferrets, and mice with and without CF. The Core will also characterize models and native epithelia in collaboration with other Cores and investigators and perform bioelectric analyses, morphological evaluation, gene expression profiles, and pH measurements in surface and luminal liquid. Finally, the Core will teach investigators at the University of Iowa and other institutions how to successfully implement the methods for in vitro model systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK054759-21
Application #
9983934
Study Section
Special Emphasis Panel (ZDK1)
Project Start
1998-09-30
Project End
2025-03-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
21
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Sweeney, Sean K; Manzar, Gohar S; Zavazava, Nicholas et al. (2018) Tracking embryonic hematopoietic stem cells to the bone marrow: nanoparticle options to evaluate transplantation efficiency. Stem Cell Res Ther 9:204
Kim, Jeeyeon; Farahmand, Miesha; Dunn, Colleen et al. (2018) Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults. Sci Rep 8:16233
Bhatt, Surya P; Washko, George R; Hoffman, Eric A et al. (2018) Imaging Advances in Chronic Obstructive Pulmonary Disease: Insights from COPDGene. Am J Respir Crit Care Med :
Bhatt, Surya P; Bhakta, Nirav R; Wilson, Carla G et al. (2018) New Spirometry Indices for Detecting Mild Airflow Obstruction. Sci Rep 8:17484
Meyerholz, David K; Beck, Amanda P; Goeken, J Adam et al. (2018) Glycogen depletion can increase the specificity of mucin detection in airway tissues. BMC Res Notes 11:763
Cooney, Ashley L; Singh, Brajesh K; Loza, Laura Marquez et al. (2018) Widespread airway distribution and short-term phenotypic correction of cystic fibrosis pigs following aerosol delivery of piggyBac/adenovirus. Nucleic Acids Res 46:9591-9600
Wang, Zekun; Cheng, Fang; Engelhardt, John F et al. (2018) Development of a Novel Recombinant Adeno-Associated Virus Production System Using Human Bocavirus 1 Helper Genes. Mol Ther Methods Clin Dev 11:40-51
Allen, Rondine J; Mathew, Basil; Rice, Kevin G (2018) PEG-Peptide Inhibition of Scavenger Receptor Uptake of Nanoparticles by the Liver. Mol Pharm 15:3881-3891
Polgreen, Philip M; Brown, Grant D; Hornick, Douglas B et al. (2018) CFTR Heterozygotes Are at Increased Risk of Respiratory Infections: A Population-Based Study. Open Forum Infect Dis 5:ofy219
Montoro, Daniel T; Haber, Adam L; Biton, Moshe et al. (2018) A revised airway epithelial hierarchy includes CFTR-expressing ionocytes. Nature 560:319-324

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