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Phenotypes of CF rabbits generated by CRISPR/Cas9-mediated disruption of the CFTR gene
Jie Xu, … , Richard C. Boucher, Fei Sun
Jie Xu, … , Richard C. Boucher, Fei Sun
Published November 24, 2020
Citation Information: JCI Insight. 2021;6(1):e139813. https://doi.org/10.1172/jci.insight.139813.
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Research Article Cell biology Pulmonology

Phenotypes of CF rabbits generated by CRISPR/Cas9-mediated disruption of the CFTR gene

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Abstract

Existing animal models of cystic fibrosis (CF) have provided key insights into CF pathogenesis but have been limited by short lifespans, absence of key phenotypes, and/or high maintenance costs. Here, we report the CRISPR/Cas9-mediated generation of CF rabbits, a model with a relatively long lifespan and affordable maintenance and care costs. CF rabbits supplemented solely with oral osmotic laxative had a median survival of approximately 40 days and died of gastrointestinal disease, but therapeutic regimens directed toward restoring gastrointestinal transit extended median survival to approximately 80 days. Surrogate markers of exocrine pancreas disorders were found in CF rabbits with declining health. CFTR expression patterns in WT rabbit airways mimicked humans, with widespread distribution in nasal respiratory and olfactory epithelia, as well as proximal and distal lower airways. CF rabbits exhibited human CF–like abnormalities in the bioelectric properties of the nasal and tracheal epithelia. No spontaneous respiratory disease was detected in young CF rabbits. However, abnormal phenotypes were observed in surviving 1-year-old CF rabbits as compared with WT littermates, and these were especially evident in the nasal respiratory and olfactory epithelium. The CF rabbit model may serve as a useful tool for understanding gut and lung CF pathogenesis and for the practical development of CF therapeutics.

Authors

Jie Xu, Alessandra Livraghi-Butrico, Xia Hou, Carthic Rajagopalan, Jifeng Zhang, Jun Song, Hong Jiang, Hong-Guang Wei, Hui Wang, Mohamad Bouhamdan, Jinxue Ruan, Dongshan Yang, Yining Qiu, Youming Xie, Ronald Barrett, Sharon McClellan, Hongmei Mou, Qingtian Wu, Xuequn Chen, Troy D. Rogers, Kristen J. Wilkinson, Rodney C. Gilmore, Charles R. Esther Jr., Khalequz Zaman, Xiubin Liang, Michael Sobolic, Linda Hazlett, Kezhong Zhang, Raymond A. Frizzell, Martina Gentzsch, Wanda K. O’Neal, Barbara R. Grubb, Y. Eugene Chen, Richard C. Boucher, Fei Sun

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Figure 1

Characterization of CF rabbit gastrointestinal function, weight gain, and mortality.

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Characterization of CF rabbit gastrointestinal function, weight gain, an...
(A) Survival curves for WT and heterozygous rabbits (black, n = 190), CF rabbits on Golytely (blue, n = 23), and CF rabbits on Golytely, Bio-Serve, and abdominal palpation-directed GI therapy (orange, n = 38). (B) Weight gain for WT rabbits (black, n = 32), untreated CF rabbits (blue, n = 17), and CF rabbits treated with Golytely starting at P14 (red, n = 15). *P < 0.05 versus untreated CF, 2-way ANOVA with Tukey’s test for multiple comparisons. (C) mRNA in situ hybridization for rabbit CFTR or negative control (RNAscope, red chromogen) on sections of WT jejunum. Scale bar: 50 μm. Representative micrographs from n = 2 rabbits. (D) Ussing chamber characterization of freshly excised jejunal tissue from WT (white bar, white dots) and CF (gray bar, black dots) rabbits at approximately P52, illustrating short-circuit currents (Isc) under basal conditions, and after forskolin stimulation (ΔFsk), bumetanide inhibition (ΔBumet), glucose addition (Δglucose), and phloridzin inhibition. n = 4/genotype, *P < 0.05 versus WT. Unpaired, 2-tailed t test with Welch’s correction for unequal variance. (E) Freshly excised WT and CF gastrointestinal tract, deconvoluted from stomach (S) to rectum (R). Asterisk represents cecum. The proximal colon (highlighted in red) was dilated in CF rabbits as compared with WT, and there was a paucity of stool pellets in the distal colon of CF rabbits. Arrow indicates a site of obstruction. (F and G) (AB-PAS stained cross section of distal colon in approximately 3 months-old WT (F) (Scale bar: 0.1 mm) and CF (G) (Scale bar: 0.1mm) rabbits, demonstrating mucus retention (arrows) in the crypts of CF rabbits. (H and I) H&E-stained cross section of distal colon in approximately 3 months-old CF rabbit (H) (Scale bar: 50 μm) and high magnification of region of interest (I) (Scale bar: 20 μm) illustrating granulocytic infiltrates (arrows) in the intestinal submucosa. Representative micrographs from n = 4 CF and 4 WT rabbits.
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