Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising/recruitment
  • Contact
  • Current Issue
  • Past Issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • Recently published
    • Technical Advances
    • Clinical Medicine
    • Reviews
    • Editorials
    • Perspectives
    • Top read articles
  • JCI This Month
    • Current issue
    • Past issues

  • Current issue
  • Past issues
  • Specialties
  • Recently published
  • In-Press Preview
  • Concise Communication
  • Editorials
  • Viewpoint
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Transfers
  • Advertising/recruitment
  • Contact
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.
View: Text | PDF
Research Article Cell biology Pulmonology

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

  • Text
  • PDF
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

×

Figure 2

Evidence of systemic inflammation in CF rabbits.

Options: View larger image (or click on image) Download as PowerPoint
Evidence of systemic inflammation in CF rabbits.
(A–C) Representative gr...
(A–C) Representative gross appearance of the vermiform appendix isolated from approximately 1-year-old WT (A) and CF (B) rabbits. CF rabbits exhibited swollen and discolored appendix as compared with WT counterparts. When cut in cross section (C), the CF appendix lumen was impacted with solid caseous material and remnants of cecal content. (D and E) Representative histology micrographs of the vermiform appendix isolated from approximately 1-year-old WT rabbit. Cross section, H&E (D) and AB-PAS (E) stain. Scale bar: 1 mm. (F) Higher magnification of the appendix mucosa in WT rabbits, H&E stain. Scale bar: 0.2 mm. (G and H) Representative histology of the vermiform appendix isolated from approximately 1-year-old CF rabbit, illustrating marked enlargement (G, H&E stain) and impaction with AB-PAS+ material (H, AB-PAS stain). Scale bar: 1 mm. (I and J) Higher magnification of the CF appendix exhibiting grossly simplified epithelial structures compared with WT, barely detectable lymphoid tissue, and intraluminal accumulation of granulocytes (arrows). H&E stain. Scale bar: 0.2 mm (I) and 0.1 mm (J). Representative micrographs from n = 5 CF and WT rabbits. (K–M) Hematologic values for WT and CF rabbits at approximately 4–5 months of age. Total hemoglobin (K), white blood cell (WBC) total (L), and differential cell counts (M). n = 19 WT (white bars, white dots) and 17 CF (gray bars, black dots) rabbits. *P < 0.05 versus WT. Unpaired, 2-tailed t test.
Follow JCI Insight:
Copyright © 2021 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts