R117H-CFTR function and response to VX-770 correlate with mRNA and protein expression in intestinal organoids

J Cyst Fibros. 2020 Sep;19(5):728-732. doi: 10.1016/j.jcf.2020.02.001. Epub 2020 Feb 13.

Abstract

Introduction: Variability in disease severity and CFTR modulator responses exists between patients with identical CFTR genotypes. Here, we characterized transcription, translation and function of R117H-CFTR using intestinal organoids and correlated them with in vitro responses to ivacaftor (VX-770).

Methods: Organoids were generated from individuals possessing at least one R117H-CFTR allele. The forskolin-induced swelling (FIS) assay was used to measure CFTR function and response to VX-770 treatment. R117H-CFTR protein and mRNA expression levels were determined in parallel and Pearson's correlation coefficients were assessed.

Results: Variability in R117H-CFTR FIS responses was observed and correlated significantly with mRNA and protein expression. Response to VX-770 treatment in organoids correlated with mRNA and protein expression as well.

Conclusions: Our results indicate that gene expression, protein expression and CFTR function are strongly correlated in organoids from people with CFTR-R117H-7T/9T, which may suggest that CFTR gene expression may have consequences for CF diagnosis, prognosis and therapeutic benefit.

Keywords: CFTR; Organoids; R117H; VX-770; mRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminophenols / pharmacology*
  • Cell Culture Techniques
  • Chloride Channel Agonists / pharmacology*
  • Colon / drug effects*
  • Colon / metabolism
  • Cystic Fibrosis / drug therapy
  • Cystic Fibrosis / metabolism*
  • Cystic Fibrosis / pathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / drug effects*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism
  • Humans
  • Organoids / drug effects*
  • Organoids / metabolism
  • Quinolones / pharmacology*
  • RNA, Messenger / metabolism

Substances

  • Aminophenols
  • Chloride Channel Agonists
  • Quinolones
  • RNA, Messenger
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • ivacaftor