Animal models of human disease are a critical component in the development of effective gene therapies. Genetically defined animal models which reproduce the clinical manifestations of a disease help to elucidate the pathophysiologically relevant cellular targets for gene therapy and aid in development and testing of gene vector technologies for therapeutic efficacy. The Animal Models Core will provide support to investigators using animal models for the development of gene therapies for several genetic diseases with an emphasis on cystic fibrosis. In this regard, the Core will provide centralized production, care, breeding, genotyping and quality control of transgenic and knockout animals for use by investigators in the Center. The core will also provide a mechanism for the receipt or distribution of new experimental transgenic and knockout models with the Jackson Laboratory Induced Mutant Resource, a national resource for transgenic and knockout mice, to Center investigators. BL2 animal containment facilities for experiments with recombinant viruses will also be consolidated within the Core for use by investigators of the Center. For CF-based research, the core will provide several animal models for cystic fibrosis, including colonies of CF mice which harbor either null or clinically relevant point mutations, and human bronchial xenografts. These models will play a large programmatic role for studies on CF airway pathogenesis and gene therapy. In addition to the obvious emphasis this Center will have in gene vector development, it is also recognized that a concrete understanding of CF airway pathophysiology is also critical to the overall goals of this Center. Such information on the basic pathobiology of CF airway disease will lead to the identification of the relevant cellular targets and CFTR functions in the lung necessary for successful gene therapy approaches. Although this Core plans to direct the majority of its efforts toward gene therapy of cystic fibrosis, it will also play a broader role in the development of gene therapies for several other genetic diseases of programmatic emphasis to this Center. The main responsibilities of the Core will be: . Generation of transgenic mice . Generation of gene-targeted mice . Genotyping transgenic and knockout animals . Rederival of genetic stocks . Maintenance, cryopreservation, and provision of genetic stocks . Quality control of genetic lines . Generation of human bronchial xenograft models.

Project Start
2001-09-01
Project End
2002-08-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
4
Fiscal Year
2001
Total Cost
$296,752
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Lynch, Thomas J; Ahlers, Bethany A; Parekh, Kalpaj R (2018) Lung transplantation: chronic rejection and stem cell depletion. J Thorac Dis 10:E666-E668
Apicella, Michael A; Coffin, Jeremy; Ketterer, Margaret et al. (2018) Nontypeable Haemophilus influenzae Lipooligosaccharide Expresses a Terminal Ketodeoxyoctanoate In Vivo, Which Can Be Used as a Target for Bactericidal Antibody. MBio 9:
Zeng, Yaohui; Singh, Sachinkumar; Wang, Kai et al. (2018) Effect of Study Design on Sample Size in Studies Intended to Evaluate Bioequivalence of Inhaled Short-Acting ?-Agonist Formulations. J Clin Pharmacol 58:457-465
Norris, Andrew W (2018) Is Cystic Fibrosis Related Diabetes Reversible? New Data on CFTR Potentiation and Insulin Secretion. Am J Respir Crit Care Med :
Metwali, Ahmed; Thorne, Peter S; Ince, M Nedim et al. (2018) Recirculating Immunocompetent Cells in Colitic Mice Intensify Their Lung Response to Bacterial Endotoxin. Dig Dis Sci 63:2930-2939
Moheet, Amir; Ode, Katie Larson (2018) Hypoglycaemia in patients with cystic fibrosis- harbinger of poor outcomes or innocent bystander? J Cyst Fibros 17:428-429
Li, Xingnan; Ortega, Victor E; Ampleford, Elizabeth J et al. (2018) Genome-wide association study of lung function and clinical implication in heavy smokers. BMC Med Genet 19:134
Kroken, Abby R; Chen, Camille K; Evans, David J et al. (2018) The Impact of ExoS on Pseudomonas aeruginosa Internalization by Epithelial Cells Is Independent of fleQ and Correlates with Bistability of Type Three Secretion System Gene Expression. MBio 9:
Janssen, Kayley H; Diaz, Manisha R; Gode, Cindy J et al. (2018) RsmV, a Small Noncoding Regulatory RNA in Pseudomonas aeruginosa That Sequesters RsmA and RsmF from Target mRNAs. J Bacteriol 200:
Janssen, Kayley H; Diaz, Manisha R; Golden, Matthew et al. (2018) Functional Analyses of the RsmY and RsmZ Small Noncoding Regulatory RNAs in Pseudomonas aeruginosa. J Bacteriol 200:

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