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Differential thermostability and response to cystic fibrosis transmembrane conductance regulator (CFTR) potentiators of human and mouse F508del-CFTR

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)L71-L86
Number of pages16
JournalAJP - Lung Cellular and Molecular Physiology
Volume317
Issue number1
Early online date24 Jun 2019
DOIs
DateAccepted/In press - 4 Apr 2019
DateE-pub ahead of print - 24 Jun 2019
DatePublished (current) - Jul 2019

Abstract

Cross-species comparative studies have highlighted differences between human and mouse cystic fibrosis transmembrane conductance regulator (CFTR), the epithelial Cl− channel defective in cystic fibrosis (CF). Here, we compare the impact of the most common CF mutation F508del on the function of human and mouse CFTR heterologously expressed in mammalian cells and their response to CFTR modulators using the iodide efflux and patch-clamp techniques. Once delivered to the plasma membrane, human F508del-CFTR exhibited a severe gating defect characterized by infrequent channel openings and was thermally unstable, deactivating within minutes at 37°C. By contrast, the F508del mutation was without effect on the gating pattern of mouse CFTR, and channel activity demonstrated thermostability at 37°C. Strikingly, at all concentrations tested, the clinically approved CFTR potentiator ivacaftor was without effect on the mouse F508del-CFTR Cl− channel. Moreover, eight CFTR potentiators, including ivacaftor, failed to generate CFTR-mediated iodide efflux from CHO cells expressing mouse F508del-CFTR. However, they all produced CFTR-mediated iodide efflux with human F508del-CFTR-expressing CHO cells, while fifteen CFTR correctors rescued the plasma membrane expression of both human and mouse F508del-CFTR. Interestingly, the CFTR potentiator genistein enhanced CFTR-mediated iodide efflux from CHO cells expressing either human or mouse F508del-CFTR, whereas it only potentiated human F508del-CFTR Cl− channels in cell-free membrane patches, suggesting that its action on mouse F508del-CFTR is indirect. Thus, the F508del mutation has distinct effects on human and mouse CFTR Cl− channels.

    Research areas

  • CFTR chloride ion channel, CFTR potentiation, cystic fibrosis, F508del-CFTR, ivacaftor (VX-770)

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via AIP at https://www.physiology.org/doi/full/10.1152/ajplung.00034.2019 . Please refer to any applicable terms of use of the publisher.

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    Licence: CC BY

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