A limitation factor in the field of cystic fibrosis (CF) has been the ineffectiveness of the CF mouse model. The recent development of the CF pig and ferret has provided additional animal models that can potentially be used to elucidate CF pathology further and to develop therapies for CF. In our preliminary work, we generated CFTR KO rabbits by using Cas9. Encouragingly CFTR null rabbits mimic human patients in several aspects including spontaneous lung infection. It is recognized that the majority of human CF patients (>70%) carry CFTR ?F508 mutation. It is further realized that CFTR?F508 protein from other species shows differences in its processing compared to human CFTR?F508 (hCFTR?F508). Thus, studies on understanding CF and developing new treatments would be further expedited with a new rabbit model expressing the hCFTR?F508.
In Aim 1, we propose to generate hCFTR?F508 rabbits.
In Aim 2, we propose to express WT rabbit CFTR (rbCFTR) in hCFTR?F508 rabbits to increase the life expectancy of the CF rabbits which is critical to fully recapitulate CF disease progression in the animals. The success of proposed work will provide an animal model for the characterization of CF pathology and the underlying molecular mechanisms. The development of therapeutic regimens would also be greatly facilitated by a model that displayed characteristic CF pathology.

Public Health Relevance

Cystic fibrosis (CF) is a life-threatening monogenetic disease. The majority of human CF patients carry the ?F508 mutation in the CF transmembrane conductance regulator (CFTR) gene. We propose to develop humanized CFTR?F508 knock-in rabbits. Successful completion of this project will establish a novel animal model for the study of CFTR biology, and facilitate the development of therapeutic strategies for CF.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21OD020187-02
Application #
9226064
Study Section
Lung Cellular, Molecular, and Immunobiology Study Section (LCMI)
Program Officer
Contreras, Miguel A
Project Start
2016-04-01
Project End
2018-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
2
Fiscal Year
2017
Total Cost
$209,250
Indirect Cost
$74,250
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109